SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs115482422 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | UBR5 | GRCh38.p7 | 8:102357457 | ACATCCTAGCTACTT[C/G]GGAGGCTGAGGCAGG | 51366 |
rs115689452 | snp | G/T | 0.0566069 | 0.158427 | intron-variant | UBR5 | GRCh38.p7 | 8:102316830 | AAACATATTATTACT[G/T]CCACAAAACACCTGC | 51366 |
rs115705110 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | UBR5 | GRCh38.p7 | 8:102266329 | TAGAGTGTATCCTGG[A/G]CATTGTGAATTAGTT | 51366 |
rs115737783 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102275006 | CTTTAAGAAATGGCT[G/T]ATTTAAGGTCTGTGA | 51366 |
rs115740103 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102316356 | TACATTTAGAAAAAA[A/G]GAAAATACATTGATG | 51366 |
rs115842451 | snp | A/G | 0.0131934 | 0.0801412 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102412236 | TGGATGGACGTCATG[A/G]TGCTTTCCTTCTCGT | 51366 |
rs115854341 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | UBR5 | GRCh38.p7 | 8:102391184 | AAAGAAAAGAAAACT[C/G]AAAGTGACAATTGTG | 51366 |
rs115856579 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | UBR5 | GRCh38.p7 | 8:102312635 | TAAAATCAACCCAGA[C/T]AGACTCTGAGCTTTG | 51366 |
rs115881330 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | UBR5 | GRCh38.p7 | 8:102370459 | CTGATAGATATATTT[A/T]TGGGGTGCATGCATA | 51366 |
rs115910068 | snp | G/T | 0.0240643 | 0.107019 | intron-variant | UBR5 | GRCh38.p7 | 8:102341614 | CTCTTTATCTGCTAG[G/T]GGGGCCCCAAAGTTC | 51366 |
rs115913298 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | UBR5 | GRCh38.p7 | 8:102383672 | AAAAGAGAAAAATGA[C/T]AAAATGGATGGGGAG | 51366 |
rs116011108 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | UBR5 | GRCh38.p7 | 8:102404038 | AAAATGTCCTGTACC[C/T]GGATTGTGGTGGTGA | 51366 |
rs116053850 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBR5 | GRCh38.p7 | 8:102296182 | CTTGGAAAACAATCA[A/G]TAACAACAGATTATC | 51366 |
rs116082545 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | UBR5 | GRCh38.p7 | 8:102260740 | ATTATTTTATGCATA[C/T]ATTTTAAAATATAAA | 51366 |
rs116148245 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102397874 | ATGGATTGGAAGAAT[C/T]AGTATTGTTAAATGT | 51366 |
rs116208802 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | UBR5 | GRCh38.p7 | 8:102390666 | TGGAAAAATGGTCTC[C/T]GAACATCCCTGTAAA | 51366 |
rs116229121 | snp | C/T | 0.0103295 | 0.0711199 | utr-variant-3-prime, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102254111 | ACTAGCAAACCAATA[C/T]AGCCAAATGTTGCTA | 51366 |
rs116231576 | snp | A/G | 0.0566069 | 0.158427 | upstream-variant-2KB, nc-transcript-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102412911 | GTCCGTTCGGCTCCC[A/G]AGCCCAGCCCCGCCG | 51366 |
rs116301227 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | UBR5 | GRCh38.p7 | 8:102355770 | TACACAGTCTGTTCT[A/G]GCAGAGAGAACAGAG | 51366 |
rs116332458 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | UBR5 | GRCh38.p7 | 8:102395051 | GTGCTGTTCCTTCTG[C/T]CTAGGGAGCTCTTCC | 51366 |
rs116395139 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | UBR5 | GRCh38.p7 | 8:102273863 | TACATACATATGCTT[A/G]TATGTTTTAAAAGGG | 51366 |
rs116402181 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102350428 | ACCCTCCTATATATC[A/G]CCAAATTATCTTACA | 51366 |
rs116460982 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | UBR5 | GRCh38.p7 | 8:102401193 | TTAAAAAAGCTTAAC[C/T]ATATCATGTCCCCGA | 51366 |
rs116478618 | snp | A/G | 0.0333238 | 0.124705 | intron-variant | UBR5 | GRCh38.p7 | 8:102369838 | AATACAATGACAATT[A/G]GTTGTACAGTTTGGT | 51366 |
rs116487520 | snp | A/C/T | 0.00597247 | 0.0543191 | intron-variant | UBR5 | GRCh38.p7 | 8:102260693 | GTTTTAGGGTCCTAC[A/C/T]GCTAATACAGTAGGA | 51366 |
rs116575695 | snp | C/G | 0.00400297 | 0.0445585 | intron-variant | UBR5 | GRCh38.p7 | 8:102265297 | ACAGAGAATATCAGA[C/G]AGTAAGCCCCAAGAT | 51366 |
rs116627439 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | UBR5 | GRCh38.p7 | 8:102316647 | CGGTGTTTCTATTCA[C/T]AAATCCCTTCAACCC | 51366 |
rs116633990 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | UBR5 | GRCh38.p7 | 8:102334446 | ACAGGTGCACGCTAC[A/C]GCACCTGGCTAATTT | 51366 |
rs116642300 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBR5 | GRCh38.p7 | 8:102349108 | CTCAAGGCTGCAGTA[C/T]GAAACAGCATTTATT | 51366 |
rs116704228 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | UBR5 | GRCh38.p7 | 8:102282527 | ACAAAAAAATTAGCA[C/T]TGTGGCGGGTGCCTC | 51366 |
rs116716307 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBR5 | GRCh38.p7 | 8:102339919 | TGTGTACAAAATTGA[A/G]ACTATCCTTTAGCAG | 51366 |
rs116788406 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | UBR5 | GRCh38.p7 | 8:102367862 | GGCTAACATAAAGAG[C/T]CACACCAGCCTTCTG | 51366 |
rs116820172 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303480 | AGCAGTGCTTCCATT[A/T]ATGATCTTGTCAAGC | 51366 |
rs116850792 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102266463 | CCAACTAAAAAGGCT[C/T]CCTTATGCTATAGCA | 51366 |
rs116855202 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | UBR5 | GRCh38.p7 | 8:102257095 | TATGGTTTTACTTGA[C/T]GGGTGGACGTAAGTT | 51366 |
rs116907639 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | UBR5 | GRCh38.p7 | 8:102341261 | AAAAAAAGTAAAAGC[C/T]CAATGGTTTAAATCA | 51366 |
rs116911745 | snp | C/G | 0.0573587 | 0.15934 | intron-variant | UBR5 | GRCh38.p7 | 8:102402035 | AGCCTGGGCAACATG[C/G]TGAAACCCCATCTCT | 51366 |
rs116912893 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | UBR5 | GRCh38.p7 | 8:102308880 | CCCTGTACATGAGTT[C/T]ACCCTGCAGTAAAAT | 51366 |
rs116947064 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UBR5 | GRCh38.p7 | 8:102336177 | TATGTCTTCTTTGAA[A/G]AAACGTCTTATAAGG | 51366 |
rs116954774 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | UBR5 | GRCh38.p7 | 8:102325615 | CTATTAACTATTACT[C/G]CATATCCCAAAAACC | 51366 |
rs117000352 | snp | A/G | 0.0573587 | 0.15934 | intron-variant | UBR5 | GRCh38.p7 | 8:102282701 | GAGGGGGTGGTGGCG[A/G]CGGGAGGATCCAAAT | 51366 |
rs117009061 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102254768 | TCACAGAGCCTCAGT[A/G]TTTTCATCTGTAACA | 51366 |
rs117009744 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | UBR5 | GRCh38.p7 | 8:102409065 | GTTTTAAGCAGGAAC[A/G]TAGTACTAACTCAAG | 51366 |
rs117016494 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102396451 | TCCAGTTCTCAGAGC[C/T]GTCTTCCATAGGGCC | 51366 |
rs117026471 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102356620 | AAAAAATTACCTGGG[C/T]ATGTTGGTGAGCACC | 51366 |
rs117061753 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | UBR5 | GRCh38.p7 | 8:102347701 | GGGGTTGCAGTAGCA[C/T]GATCTCGGCTCACTG | 51366 |
rs117088075 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UBR5 | GRCh38.p7 | 8:102373071 | AGCTCTCGAACTCCT[A/G]GGCTCAAGCTGTCCT | 51366 |
rs117103565 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102256626 | CTAAGTCAAAATTAC[A/T]AGGGTGGCTAAAAGC | 51366 |
rs117104586 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBR5 | GRCh38.p7 | 8:102392691 | ATCAGAATATAGTGA[C/T]AAGAACTAGTTTTTA | 51366 |
rs117109841 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102355541 | GTAAAAAAAAAATTT[G/T]ATTTACAAAATAACT | 51366 |
rs117150973 | snp | C/T | 0.00212575 | 0.0325324 | intron-variant | UBR5 | GRCh38.p7 | 8:102287391 | AATACACACACACAG[C/T]CTTAGCATAAGCAAG | 51366 |
rs117159903 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | UBR5 | GRCh38.p7 | 8:102333932 | TTCTTACTTCATATT[A/G]AATTACATTTGTGAC | 51366 |
rs117198831 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UBR5 | GRCh38.p7 | 8:102375820 | CCTGGCTGTCTAAGC[A/G]CCTTACATTGGTAAC | 51366 |
rs117230160 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303463 | CACATTAGCACATAG[C/T]GAGCAGTGCTTCCAT | 51366 |
rs117250487 | snp | A/G | 0.0573587 | 0.15934 | intron-variant | UBR5 | GRCh38.p7 | 8:102354504 | CATCTATTGTTCAAC[A/G]GTCACAAGTAACAGA | 51366 |
rs117285004 | snp | A/G | 0.046122 | 0.144685 | intron-variant | UBR5 | GRCh38.p7 | 8:102280501 | GTCATTTTACTTGAA[A/G]TATTTGTATAATATG | 51366 |
rs117294140 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102362878 | TTTTTTTTTTTTTGA[A/G]TCTCGATCTGTTGCC | 51366 |
rs117303721 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBR5 | GRCh38.p7 | 8:102394355 | GCGAGCCACCGCATC[C/T]GGCCAGAATTTATTC | 51366 |
rs117323662 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102257323 | AAAGGATTAAGGATG[C/T]ATACAGGGAGAAGCA | 51366 |
rs117335022 | snp | C/T | 0.0569829 | 0.158885 | intron-variant, downstream-variant-500B, nc-transcript-variant | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102251910 | AAGAATCTGCATTAA[C/T]AAACTTTACAAATGA | 51366 |
rs117338069 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102297329 | TTTTGCCTCATTTAC[C/T]TAGGAATTAAATCAA | 51366 |
rs117338901 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102379076 | GGAAATCACTTGCTA[A/G]TTACAGAGATACATC | 51366 |
rs117385805 | snp | A/G | 0.0573587 | 0.15934 | intron-variant | UBR5 | GRCh38.p7 | 8:102268719 | CAGGAGGGTATTCTG[A/G]TAAGTGAATTTGAGA | 51366 |
rs117387999 | snp | C/G | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102347883 | CCTCCCAAAGCGCTG[C/G]GAAAATAATTTTTTA | 51366 |
rs117401820 | snp | C/T | 0.0573587 | 0.15934 | intron-variant | UBR5 | GRCh38.p7 | 8:102397041 | TCTGTGAGAACAGCA[C/T]TTGAAGAGGCCACAT | 51366 |
rs117436093 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102270710 | TTTTAGGAAAGACAG[A/G]GTTTCACCATGTTGG | 51366 |
rs117447530 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102352937 | TACACAAGCCCTCCA[C/T]TGAGTTTAAAGACAA | 51366 |
rs117449180 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102339862 | GTTTCCTTCTCCATA[A/C]AAATGAATGGATCAG | 51366 |
rs117473148 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102278554 | TATTTTTATTATACA[C/T]GAAAAATTCAAATTT | 51366 |
rs117512916 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102300389 | ATATTAAGCTCCCAC[A/C]CAAACTTAAGCACAG | 51366 |
rs117540117 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | UBR5 | GRCh38.p7 | 8:102271383 | CCCTAGCATCTGTGT[C/T]GTTAATGCCTTTCTC | 51366 |
rs117540257 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102280204 | ACATTTCTTTAATAC[A/G]TCCTTAGTTGTGAAA | 51366 |
rs117557182 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102323221 | GTTTACAACTTCACA[C/T]CTCTAAGTCTTCCTT | 51366 |
rs117576089 | snp | A/G | 0.0573587 | 0.15934 | intron-variant | UBR5 | GRCh38.p7 | 8:102288477 | GAGACGGAGATGGGC[A/G]GATCACAAGGTCAAG | 51366 |
rs117576519 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBR5 | GRCh38.p7 | 8:102364419 | ACTCCTGGGCTCAAC[A/G]GATCTACTTGTCTTG | 51366 |
rs117586464 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102301435 | ATTAAAAAATAACTA[C/T]AGTTAATTATTTTAT | 51366 |
rs117586916 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102256912 | GATCATTTTTAAATA[C/T]TTCCAGAAGTGGTCT | 51366 |
rs117595392 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | UBR5 | GRCh38.p7 | 8:102400035 | CCAAAAATATCTGGC[A/G]TAATATGTTACCATT | 51366 |
rs117617560 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102314913 | TAATGGAAACTAGTA[C/T]TTTTTAAAGACAAGT | 51366 |
rs117638395 | snp | C/T | 0.084728 | 0.187577 | intron-variant | UBR5 | GRCh38.p7 | 8:102390189 | TGAATAGTACATGTT[C/T]GCTCAAAATAAAAGC | 51366 |
rs117645205 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102306487 | GTGAGACAGGCCACT[C/T]TGATTGTGGAACTAA | 51366 |
rs117652749 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | UBR5 | GRCh38.p7 | 8:102351995 | CTAAAATAAGTTTTT[A/T]AATTGTTTTTAAAAT | 51366 |
rs117681718 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | UBR5 | GRCh38.p7 | 8:102273930 | ACAAGAATGGACTTA[C/T]ATCCATTCTTTTGTA | 51366 |
rs117693930 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | UBR5 | GRCh38.p7 | 8:102283577 | AGAATTCTGTGTTCT[C/G]TGGGGTAACAACTAC | 51366 |
rs117695477 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | UBR5 | GRCh38.p7 | 8:102344011 | ACACTATTACATAGT[A/G]CATTCAATATATTAA | 51366 |
rs117717567 | snp | A/T | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102255283 | GAAAAGCTTTTTTTT[A/T]AATCTAATCATTTTA | 51366 |
rs117725033 | snp | A/T | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102357293 | TCATGGCCAGAAAGA[A/T]AAAGACTGAGGATCT | 51366 |
rs117739535 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBR5 | GRCh38.p7 | 8:102309958 | TAGTACTCTCAGCAC[A/G]TCATAAGGAATCCTT | 51366 |
rs117766015 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | UBR5 | GRCh38.p7 | 8:102326399 | TACAGTATTACTCTA[C/T]TGAATGAAGGAAGAA | 51366 |
rs117768146 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102274391 | TTGATTAATGTTGTT[A/G]GGAAGTTGGCTATTC | 51366 |
rs117770744 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102271012 | TCTTAGTTACTATAC[A/G]TATGTTCAAAATTAA | 51366 |
rs117775774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102398391 | AAAAACTGGGAAAAC[C/T]CTCCAGGACACTGGA | 51366 |
rs117782297 | snp | C/T | 0.100588 | 0.200439 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102411705 | CGGGACAAGCCCAGC[C/T]CAGCCCACCCCGGGG | 51366 |
rs117797594 | snp | G/T | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102270239 | ACTAACAAGTAAAAA[G/T]ATTAGCACAACTAGT | 51366 |
rs117820249 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | UBR5 | GRCh38.p7 | 8:102284097 | TTGACTTCAGGTATG[A/G]GGCACTTTTACTATA | 51366 |
rs117822368 | snp | A/T | 0.0399052 | 0.1355 | intron-variant | UBR5 | GRCh38.p7 | 8:102260036 | TGTCTTAAAAAAAAA[A/T]ATATTTTTTTTTACC | 51366 |
rs117858984 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | UBR5 | GRCh38.p7 | 8:102359814 | GAAATAAATGGCGTG[A/T]CATTATAAACATATG | 51366 |
rs117861413 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | UBR5 | GRCh38.p7 | 8:102297150 | AAATATACAGTTTAT[A/G]ATATACAAATAGAAA | 51366 |
rs117889583 | snp | A/G/T | 0.0329836 | 0.124112 | intron-variant | UBR5 | GRCh38.p7 | 8:102284765 | TTGGGGGTCGGGCGC[A/G/T]GTGGCTCACGCCTGT | 51366 |
rs117890049 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102353083 | CTACCAGTCCCCGTA[C/T]GTCAATCGCCATTAA | 51366 |
rs117915041 | snp | A/C | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102260858 | TACCACTAAAACAGT[A/C]GGACCCTAAAACAGT | 51366 |
rs117933759 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102284089 | CTTGGATTTTGACTT[C/T]AGGTATGAGGCACTT | 51366 |
rs117947562 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | UBR5 | GRCh38.p7 | 8:102307025 | GATGACTCTACCTGT[C/T]AGATCCTGACAAAGT | 51366 |
rs117983544 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBR5 | GRCh38.p7 | 8:102364206 | GCCTCTTTTGAGACT[A/G]GGTCTCACTCTGTCG | 51366 |
rs117997731 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | UBR5 | GRCh38.p7 | 8:102325902 | TTCAATCTGTTGATA[C/T]CTTCTTCTGACAAAG | 51366 |
rs118009291 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102273668 | AGCCCAAATACCTAG[A/T]CTGTAAGGGATTAGC | 51366 |
rs118045329 | snp | A/T | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102391084 | CAAAGTGGGAGAATC[A/T]CTTCAGCCTGGGAGG | 51366 |
rs118073779 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102307777 | ACACAGTTGGTCCCA[A/G]CATCCTGCTTGACAT | 51366 |
rs118075062 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | UBR5 | GRCh38.p7 | 8:102299646 | TCTCTGCAAGCCAAA[A/G]GTCAAATTGGATAGA | 51366 |
rs118132857 | snp | C/G | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102273385 | AACTATACTGAGGTG[C/G]TATTTCTTACCTATT | 51366 |
rs118150328 | snp | C/G | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102356214 | TAGCACTTTGGGAGG[C/G]TAAGGCAAGGAGATC | 51366 |
rs118170050 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102384675 | AAACACACACACACA[A/T]ATTTAGGGACAAGTC | 51366 |
rs118179276 | snp | A/T | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102348130 | TCGGGAGGTTGAGGA[A/T]GAACTGCTTGAACCA | 51366 |
rs137885788 | in-del | -/A | 0.103082 | 0.202275 | intron-variant | UBR5 | GRCh38.p7 | 8:102389486 | CTACATGAGAAACAT[-/A]AGAGTAAGAACCACC | 51366 |
rs137898888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102349784 | ATGAATTGAAAGACC[A/G]AATATTGCTAAGAGG | 51366 |
rs137899532 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBR5 | GRCh38.p7 | 8:102332333 | TGCTTTCTCCCATCA[C/T]GCCAGTAATGTTCAC | 51366 |
rs137906088 | in-del | -/A | 0.186592 | 0.241835 | intron-variant | UBR5 | GRCh38.p7 | 8:102278803 | TAAATGTTATATTGC[-/A]AAAAAAACTTTTACT | 51366 |
rs137921349 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102272539 | CTTACTTGTGTGGGT[A/G]CCTTTGTTGGCATTT | 51366 |
rs137923050 | snp | A/C | 0.0225045 | 0.103662 | intron-variant | UBR5 | GRCh38.p7 | 8:102259950 | GGAGAATCACTTGAA[A/C]CCAGGAGGCGGAGGT | 51366 |
rs137940203 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102291507 | CCCCCTCACATATAT[A/C]AAGCTAAACATAAAT | 51366 |
rs137942152 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102384280 | GCAATGATTCTCATC[C/T]TTTCTTCAAAGGTGA | 51366 |
rs137942616 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | UBR5 | GRCh38.p7 | 8:102256130 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 51366 |
rs137973554 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBR5 | GRCh38.p7 | 8:102409221 | AAGTCACAGCCAACA[C/T]CCTCTTCTTTCCACC | 51366 |
rs138009606 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102362624 | AAATGTTATACATAC[G/T]CCAAAAATAAATGAC | 51366 |
rs138028570 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102326419 | TGAAGGAAGAATGAC[A/G]TGACACATACACGTT | 51366 |
rs138052105 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102319485 | TCCCACACACAATAA[C/T]AATGGGAGACTTTAA | 51366 |
rs138054497 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102376901 | GGAACTCACTACTCA[C/T]TCTAAAACACCATAA | 51366 |
rs138071649 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBR5 | GRCh38.p7 | 8:102405689 | CCAGGTATGGTGGCG[C/T]GCGCCTGTACTCCCA | 51366 |
rs138091752 | in-del | -/ACAATGTGTATACATGTAT | 0.137867 | 0.223442 | intron-variant | UBR5 | GRCh38.p7 | 8:102370491 | AACATGTACATGTAC[-/ACAATGTGTATACATGTAT]ACAATGTGTTAATAA | 51366 |
rs138133275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102273782 | GGATATACTACTAAG[C/T]GAGAAAAGCAAGATG | 51366 |
rs138209681 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | UBR5 | GRCh38.p7 | 8:102335537 | ATACACAATAAAATT[C/T]ATTTATTTATTTAGT | 51366 |
rs138234146 | in-del | -/TTTG | | | intron-variant | UBR5 | GRCh38.p7 | 8:102310341 | TTTTTTAAAATGTTT[-/TTTG]TTTGTTTGTTTGTTT | 51366 |
rs138247504 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | UBR5 | GRCh38.p7 | 8:102397181 | ACTGAAGAGGATAAA[A/C]CAGTCCCCACATCCT | 51366 |
rs138265094 | in-del | -/ACA | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102311093 | CCCCTTTGTGCTCCT[-/ACA]ACATTATGCATGCCT | 51366 |
rs138277264 | snp | C/T | 0.0110788 | 0.0735978 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102293637 | TGATGGTCGTGGTGG[C/T]AGTGGTTCCACTGAA | 51366 |
rs138283971 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UBR5 | GRCh38.p7 | 8:102310439 | GCAACCTCCGCCTCC[A/G]GGGTTCAAGTGATTC | 51366 |
rs138292092 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102297901 | CAACTCCTGGCTCTA[C/T]TTAGCAAATTATAGA | 51366 |
rs138335237 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102351181 | GATCCAGCAATTGCA[A/T]GTCTGGTATATATTC | 51366 |
rs138376624 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | UBR5 | GRCh38.p7 | 8:102337699 | AGGATTTCTGCATCA[A/G]TGTTCAAAGATATTA | 51366 |
rs138376644 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102391675 | CTCCATCTACAATCC[C/T]TAGGATTAAATGTTT | 51366 |
rs138396904 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | UBR5 | GRCh38.p7 | 8:102336710 | CCATTGGTCTATGTT[G/T]CTGTTTTTACGCCAG | 51366 |
rs138441844 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102320062 | aacacattcaaaagc[G/T]agcagaaggcaagaa | 51366 |
rs138447031 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102388540 | GTATCAGAAGAGTAA[C/T]GTGCTGATGACGTCA | 51366 |
rs138465095 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBR5 | GRCh38.p7 | 8:102262268 | TATTTGCTTTTCAAA[A/G]TATAAGAAGGGTTAT | 51366 |
rs138473888 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102388440 | TAGTATTTCAGTGCA[A/G]ACATGTCTCTGAAAA | 51366 |
rs138518996 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | UBR5 | GRCh38.p7 | 8:102263442 | CATTTGTTTTGTGTC[A/C]AGTAATTTCTCTAAA | 51366 |
rs138542317 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102314656 | AGATGTAAAAAATGA[A/C/T]ATGAGTTGCCTTAAA | 51366 |
rs138542461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102260200 | TTTTGAATGTCTGGA[A/G]CAATGAACCATGCTG | 51366 |
rs138553849 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102399726 | CCAAAGCGGGTGGAT[C/G]ACGAGGTCAGGAGTT | 51366 |
rs138564113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102305356 | TAGCACATTACATAT[A/G]TTAAAAATTTCTCAT | 51366 |
rs138565877 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102400867 | CCCTATTCTCAAACA[C/G]ACAGGTATAAAACCT | 51366 |
rs138585686 | snp | C/G/T | 6.78179e-05 | 0.00582282 | intron-variant | UBR5 | GRCh38.p7 | 8:102279236 | AGATAAAATGTTTTG[C/G/T]TTTTTAGGAAAATTA | 51366 |
rs138608853 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102332003 | CTCCAGACTTACCTA[C/G]AGCTGTCTTAAAAAG | 51366 |
rs138660819 | snp | C/T | 0.0752113 | 0.178743 | intron-variant | UBR5 | GRCh38.p7 | 8:102284990 | TGCAGTGAGCCGAGA[C/T]GGCACCACTGCACTC | 51366 |
rs138664410 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | UBR5 | GRCh38.p7 | 8:102372843 | TAGAAATTCTTATAT[C/T]GTACCACAAATAACA | 51366 |
rs138678186 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102403924 | GAAAAGCATTACAGT[A/G]AGAGAAAGCAGAACA | 51366 |
rs138706820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102368195 | TGCAATAAATAAACA[C/T]AAAATTAGCTATATT | 51366 |
rs138846718 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | UBR5 | GRCh38.p7 | 8:102278327 | CCCACGTGAAATTTA[C/T]TTACTCTCTTCAAGA | 51366 |
rs138866633 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102274134 | AATTTAACTGTGTAT[A/C]TCTAACTGCATATGA | 51366 |
rs138876898 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102366671 | CTAAGTAACTCAATA[A/G]TCATATTAGGAAACT | 51366 |
rs138913761 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102305268 | CCTCATAGTCACAGC[A/G]CAGAATGTGTTGCAT | 51366 |
rs138947567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102306697 | TGTACGGTGCTGTCA[C/T]ATACACTGGTTTCAA | 51366 |
rs138949643 | snp | C/T | 0.162909 | 0.23434 | intron-variant | UBR5 | GRCh38.p7 | 8:102267952 | GCTGGAGTGCAGTGG[C/T]GCAATCTCAGCTCAC | 51366 |
rs138950302 | in-del | -/AAAGAA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102269615 | TGTTTCATATCATAT[-/AAAGAA]AAACTCTTGATAGAA | 51366 |
rs138955927 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | UBR5 | GRCh38.p7 | 8:102391959 | TCTGGTAATCCTCAC[G/T]GCTATACTCCCAACA | 51366 |
rs138981701 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | UBR5 | GRCh38.p7 | 8:102344995 | GGTCCTAAATCCATT[C/G]TAGTAAGTTTTTTCA | 51366 |
rs139028385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102276167 | TCAAACTTTCACCAT[A/G]AACCAGAATCTCCAT | 51366 |
rs139029258 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102355891 | AGCCCTAATCTTCTT[A/C]AGAGTAGGTCTACAG | 51366 |
rs139033356 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | UBR5 | GRCh38.p7 | 8:102264023 | CAGGCATAAGCCACC[A/G]TGCCTGGCCTGGAAG | 51366 |
rs139050981 | snp | G/T | 6.61212e-05 | 0.00574945 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102323369 | TTTCAGGAGATCTAA[G/T]TTGAAATCTACAGCT | 51366 |
rs139054299 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | UBR5 | GRCh38.p7 | 8:102312660 | GCTTTGCTACTGACA[A/T]CTATATTCAAGGCTC | 51366 |
rs139060173 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102411560 | CCTCCCTCACTCCCT[C/T]CCCCAACTATCACCT | 51366 |
rs139071756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102400262 | TCAAGATCAGCCTAG[A/G]CAACACAGCAAGACC | 51366 |
rs139159922 | snp | A/G | 0.000263913 | 0.0114842 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295511 | GACTGTCTGTACTAA[A/G]AATAGTAAGAGGTGC | 51366 |
rs139294055 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBR5 | GRCh38.p7 | 8:102271325 | AGTCAATGCAAAGAA[A/G]TGAGACAAATGTAAG | 51366 |
rs139308706 | snp | C/G/T | 4.94599e-05 | 0.00497272 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102272697 | CAGCCATTGGTGTAG[C/G/T]AGCACATCTTCGACC | 51366 |
rs139342336 | snp | C/T | 9.44465e-05 | 0.00687127 | intron-variant | UBR5 | GRCh38.p7 | 8:102264608 | ATTCTAGAATACATA[C/T]ATCCCCCCACACATA | 51366 |
rs139369208 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102360457 | TTAAACTAGAAAGCA[A/G]TAGTTTCACTGTTTT | 51366 |
rs139374487 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102333777 | TACTGCACATCATGA[C/T]TGGAATGATGGCAAC | 51366 |
rs139388069 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102401527 | AAAGTAGCAGAAAGA[C/T]GAACAGATGCCAACA | 51366 |
rs139434916 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102316477 | TTTAACAATTTTACT[A/G]AAGTTTTAAAGTTCA | 51366 |
rs139441145 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102405772 | TGCAGTGAGCCAAGA[C/T]TGTGCCAAAATGGCA | 51366 |
rs139457107 | in-del | -/AG | 0.497881 | 0.0324789 | intron-variant | UBR5 | GRCh38.p7 | 8:102392815 | AATGAGCCTGTTATC[-/AG]AGGTCTCCCCACAGC | 51366 |
rs139470413 | snp | C/G | 0.0279526 | 0.114869 | intron-variant | UBR5 | GRCh38.p7 | 8:102381043 | GAGAGAGAAAGCAAA[C/G]GAGAACAGGGAAAAC | 51366 |
rs139485637 | snp | C/T | 0.0238149 | 0.106492 | intron-variant | UBR5 | GRCh38.p7 | 8:102327696 | AAGCATCTTTCTATA[C/T]ATACACAAGCATTCA | 51366 |
rs139611652 | snp | A/T | 1.64942e-05 | 0.00287173 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102281471 | ATAATTTAGGAAGTC[A/T]CCTCGTGCAGACATC | 51366 |
rs139631475 | in-del | -/AC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102287379 | CAATCCACGCTGAAT[-/AC]ACACACACAGCCTTA | 51366 |
rs139636615 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102271944 | TTTTGTAATTTTCAC[A/T]AATTTTAAAATTTGA | 51366 |
rs139708842 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102293693 | CATCTATGCTAGTAC[C/T]AGCCAGGGTAAATGG | 51366 |
rs139724709 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102386704 | TCATATAGGCCGGGC[A/G]CGGTGGCTCATGCCT | 51366 |
rs139791656 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | UBR5 | GRCh38.p7 | 8:102357937 | GATCACCTGAGGTCC[A/G]GAGTTCAAGACCAAC | 51366 |
rs139798359 | snp | C/G/T | 0.00557734 | 0.0525397 | intron-variant | UBR5 | GRCh38.p7 | 8:102311185 | GACCATTAGCTCTTT[C/G/T]AGGGAAGAAAGGGGC | 51366 |
rs139840602 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102329713 | CCCTCAAGAGACTGT[C/T]TCTGATGACACTATG | 51366 |
rs139854203 | in-del | -/G | 0.00874735 | 0.0655527 | intron-variant | UBR5 | GRCh38.p7 | 8:102285988 | AAATCTGACCCCCAC[-/G]CCACCTCCCCCCGCC | 51366 |
rs139860593 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102257902 | AACCTCTACAGTTCA[C/T]TAGTCAATCCTGACT | 51366 |
rs139899317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102307318 | GTAACCCATCAAGAA[C/T]TCTAAAATGATATGA | 51366 |
rs139899339 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102252345 | AAAATCTTTTACTAT[G/T]ATTAGAAGTATTTTT | 51366 |
rs139914688 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102315883 | TGATTTCAAGGAAGA[G/T]CTTGAAAAACTTCAT | 51366 |
rs139934737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102312124 | CAGCTGAAGAAGTTT[C/T]AAAATTTACCTTTGG | 51366 |
rs139952877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102256457 | AGGTGCCCTGAATCT[A/G]AAGACTGACTAAAGG | 51366 |
rs139955761 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102389203 | CTAGCCTGATGACTT[C/G]CTTCTTGCAAAGGTA | 51366 |
rs139974948 | in-del | -/AC | 0.0573587 | 0.15934 | intron-variant | UBR5 | GRCh38.p7 | 8:102266850 | ATTTTATTTATAAAG[-/AC]AGTTTCTTCAGAAAT | 51366 |
rs139982998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102363453 | AACCCATGAGCTCTA[A/G]GAGAAGGCTGACTAG | 51366 |
rs139991906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102301461 | TTTATAGTATCAATG[C/T]CTTCTTTTTCCAATT | 51366 |
rs139998422 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBR5 | GRCh38.p7 | 8:102334378 | CTCACTGCAACCTCC[A/G]CCTCCTGCGTTCCAG | 51366 |
rs140042629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102374981 | AAACGGACATTCATG[C/T]CTTAGCTCTAAGCCC | 51366 |
rs140062532 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102379821 | CTAAATATGTAGCTA[-/T]TGAAAGGCAACTGTA | 51366 |
rs140099819 | snp | C/T | 8.3176e-05 | 0.00644834 | intron-variant | UBR5 | GRCh38.p7 | 8:102342444 | AGGGATCCATTTAAA[C/T]GGAAGCAGTGTGAAT | 51366 |
rs140124086 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102291775 | CTCTGCCATCTACTA[C/T]TCAGGAGAATACAAA | 51366 |
rs140143640 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102286756 | AAACCTACCATAAAA[C/T]AGTTTTTATTAGAAA | 51366 |
rs140193494 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102338125 | GTGAGTAAAGGGAGC[A/G]GGAAAAAGGAGTCGG | 51366 |
rs140195197 | snp | A/G | 1.65007e-05 | 0.00287229 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102270159 | AAAGGGCCTAGTGTC[A/G]ATGGAAAGCTGTCTT | 51366 |
rs140212916 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102266107 | TTTAATTCTAAAAAT[G/T]TCCCTTTGTTCTCTT | 51366 |
rs140213243 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102259899 | TGGGCATGCTGGCGC[A/G]CGCCTATAGTCCCAG | 51366 |
rs140280535 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102305709 | TGATAGCCAATTAAG[C/G]AAAGGATATAAATTT | 51366 |
rs140284966 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102391442 | GTTAATTTCCTATAA[A/C]GTGTGATAATGGTAA | 51366 |
rs140340753 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102374883 | AACAAACTCTTAAGG[A/C]AAGAACTATGTTTTA | 51366 |
rs140345531 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303375 | AAGAATACACATTTT[A/T]AAAGGAATAGTTAAC | 51366 |
rs140381022 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102369385 | AGTATGATTTTGTCA[C/T]CTGGACCAGGATACA | 51366 |
rs140391619 | in-del | -/CAT | 0.0182019 | 0.0936463 | intron-variant | UBR5 | GRCh38.p7 | 8:102379299 | GTAAAACGCGGTCGC[-/CAT]CATCATAGCTACAAT | 51366 |
rs140422134 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102325218 | AACTAATATAAATAA[C/T]GAAGGCCGATCAATA | 51366 |
rs140432013 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102261907 | AGAAAAGTGTATATT[G/T]GCTTTACCTGTCCTC | 51366 |
rs140432729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102407791 | TATATTGCTTGAAAT[A/G]TTCTTCATAAAAGTC | 51366 |
rs140441478 | snp | C/T | 0.000580292 | 0.0170238 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102312222 | ACAGTCGGGAACCTT[C/T]GGTGTTCCACCAGTT | 51366 |
rs140487941 | in-del | -/AC/CA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102261701 | TCCATCTCACACACA[-/AC/CA]CACACACACAAAAAG | 51366 |
rs140532509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102402509 | TAACCCTACCATATT[A/G]TCTGGGCTTTCTTAG | 51366 |
rs140557529 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102375800 | AAGCCTATTATAGTG[C/T]AGAGCCTGGCTGTCT | 51366 |
rs140559277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102283691 | AGTACAGCTATCTTT[A/G]CCAAGCATTCAATTC | 51366 |
rs140597277 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | UBR5 | GRCh38.p7 | 8:102371642 | CGCCCAGGCTGGAGT[A/G]CAATGGCACGATCTC | 51366 |
rs140599016 | snp | A/C | 0.00101056 | 0.0224557 | intron-variant | UBR5 | GRCh38.p7 | 8:102278790 | CAAGTTGTCCTTAAT[A/C]AATGTTATATTGCAA | 51366 |
rs140601769 | snp | C/T | 3.32851e-05 | 0.00407939 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102286373 | GCCTGCTGGTGTAGA[C/T]GTACTGGAAGGGGCT | 51366 |
rs140621274 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102273695 | TAGCTGCAAAAACTG[C/T]GATAACAACCATTAA | 51366 |
rs140640466 | snp | A/G | 1.651e-05 | 0.0028731 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102347047 | AGCTGATGACCTACC[A/G]GAGGATCCTCCACCA | 51366 |
rs140655616 | in-del | -/AT | 0.226188 | 0.248863 | intron-variant | UBR5 | GRCh38.p7 | 8:102396622 | TATATCTAAATTCAA[-/AT]ATATATATATACACA | 51366 |
rs140710235 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102388421 | AAATGAATACACACA[A/C]TAGTAGTATTTCAGT | 51366 |
rs140744625 | snp | A/G | 0.000262556 | 0.0114546 | intron-variant | UBR5 | GRCh38.p7 | 8:102296856 | AAATCTAAACAGCTT[A/G]TAATATTAAACTAAA | 51366 |
rs140747021 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102262224 | AACTATTTAAAGAGA[G/T]AAGTTTAATAAATCT | 51366 |
rs140747291 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102351459 | GTTCCACTTATATGA[A/G]GCATCTTAAATAGAC | 51366 |
rs140767462 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102313221 | GTATATCTGCTCTTT[A/C]CTTTAAGTATAAATG | 51366 |
rs140769614 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102398928 | GCTCAAACAACTCTA[C/T]AAGAAAAAATCTAAT | 51366 |
rs140814150 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102331733 | CTCTTCAAATGATTT[C/G]CCTCTGTTCATTATC | 51366 |
rs140838937 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102258102 | TTTCAGATGATGCCA[A/G]TGCTACTGATCTGAG | 51366 |
rs140845666 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102259387 | TCCCAGTGATTTAAC[A/G]ATTTTAAAAGTTTTG | 51366 |
rs140887830 | snp | C/T | 0.00835141 | 0.0640778 | upstream-variant-2KB, nc-transcript-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102412906 | GATTGGTCCGTTCGG[C/T]TCCCGAGCCCAGCCC | 51366 |
rs140889026 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102350513 | TGGGAAAAGTGGATA[A/T]CCACATGCAAAAGAA | 51366 |
rs140917951 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102370924 | CTCCTGGCTCATCCA[C/T]GTTGTTGCAAATGAC | 51366 |
rs140921725 | in-del | -/GAG | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102266607 | TGGGATTACAGGCGT[-/GAG]GAGCCACCACACCTG | 51366 |
rs140966610 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102407203 | CAACCTCTGCCTCAC[A/G]GGCTCAAGCTCTGTC | 51366 |
rs141040700 | in-del | -/GC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102326896 | GGAAATTCATCAATT[-/GC]TTTTTTTTTTTTTTT | 51366 |
rs141094542 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102384125 | AGCCTTTTTGAAAAC[A/G]ACACAGAACTTTCTA | 51366 |
rs141130667 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102308511 | ATTGCCTAGTGACAT[C/T]GTAGCTGTTGTTAAA | 51366 |
rs141134307 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102291186 | AGCCCCGTTAATACA[C/T]TACTAAGTTTTGGGG | 51366 |
rs141167447 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBR5 | GRCh38.p7 | 8:102277659 | CGCTGGGATTACAGG[C/T]ATAAGCCAGCACAAC | 51366 |
rs141255965 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102331187 | TCCCAGTGAACAGGA[A/G]GCTATAATAAGTTTT | 51366 |
rs141289790 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBR5 | GRCh38.p7 | 8:102339553 | AAAAAAGGTAAAATT[C/T]TGAAGAACTGGTTGT | 51366 |
rs141291363 | in-del | -/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102392606 | CAGGACTATTAGATA[-/C]CAAAAAAAAAAAAAA | 51366 |
rs141291501 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102253064 | AAAACAAAAACCTGT[C/T]AGTTATTAGGTGTAA | 51366 |
rs141291939 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102325603 | TTCCTTTTTTCACTA[C/T]TAACTATTACTGCAT | 51366 |
rs141323060 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102263718 | AGTTAGAATGCTCTA[-/T]TTTTTTTTTTGTTTT | 51366 |
rs141324821 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBR5 | GRCh38.p7 | 8:102275314 | AATTTGGTGGTTACA[A/G]TAAGAAAAAAATAAA | 51366 |
rs141335442 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | UBR5 | GRCh38.p7 | 8:102395758 | GGTAATATCTATTAC[A/C]GTCTAATACACAGAA | 51366 |
rs141367959 | snp | A/C/T | 9.88393e-05 | 0.00702929 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102305211 | GTAGATTCTGCTCTA[A/C/T]AACAACCGCTTGCTC | 51366 |
rs141375309 | snp | C/G | 0.00239568 | 0.0345268 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102411280 | TTGCGAACTGCAAAC[C/G]TAAGAGTTTTCCTTT | 51366 |
rs141383011 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102335431 | TAGCTGCTCTTGTCA[C/G]AAAATAGTAACTGTG | 51366 |
rs141401101 | in-del | -/C | 0.17654 | 0.238964 | intron-variant | UBR5 | GRCh38.p7 | 8:102297841 | TACAAACACACTATA[-/C]ATCAGCCATCTGAAT | 51366 |
rs141421835 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | UBR5 | GRCh38.p7 | 8:102388099 | AAAAACTGCAAAATA[C/T]CCAAGAAAAATGGCA | 51366 |
rs141425108 | snp | A/G | 1.64863e-05 | 0.00287104 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102326576 | GATGTTCGGCATTGA[A/G]GAAATACCAGCACTG | 51366 |
rs141456945 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102315670 | ACATGAGTGATCTCA[A/G]TAAGTACACAGCAAA | 51366 |
rs141462658 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102400325 | ATACATGGCATACCC[A/C]CCTGATGCCACTCCC | 51366 |
rs141504596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102333331 | TGTTTTTATGAAGTA[C/T]GAATTGCTGCTTCTT | 51366 |
rs141518502 | snp | C/T | 0.00011578 | 0.00760767 | intron-variant | UBR5 | GRCh38.p7 | 8:102360544 | GGTTTAATATAATAC[C/T]TAAGAGCTAAATACA | 51366 |
rs141523143 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102350946 | CAAATGAAAAGATGT[C/T]TAACACCATTAATCA | 51366 |
rs141542961 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBR5 | GRCh38.p7 | 8:102260124 | CTAGTAGGGCTGGCA[C/T]TGGCTGGTGTCTGAG | 51366 |
rs141570508 | snp | C/T | 0.165527 | 0.235296 | intron-variant | UBR5 | GRCh38.p7 | 8:102396667 | ACACACACACACACA[C/T]ATATATATATATACA | 51366 |
rs141581167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102256052 | ATACTGGTTTAAAAA[C/T]GGCAGAATTGGGAGG | 51366 |
rs141700512 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102317328 | TACGCTCAGAGTCTC[A/G]CTGATTGCTAGCACA | 51366 |
rs141717308 | snp | C/G | 0.084728 | 0.187577 | intron-variant | UBR5 | GRCh38.p7 | 8:102319154 | GGCAAATTGGATAAA[C/G]AGTCAAGACCCATCA | 51366 |
rs141759042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102316088 | GACAGAGAAAGAACA[C/T]GAAAACTAAAAGCAA | 51366 |
rs141784223 | snp | A/G | 0.093777 | 0.195178 | intron-variant | UBR5 | GRCh38.p7 | 8:102319727 | AAAAGATCAGAAATT[A/G]TAACAAACTGTCTCT | 51366 |
rs141792872 | snp | C/T | 0.000971489 | 0.0220182 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102313849 | CACAAAAACCACTTC[C/T]CGAAGAGACCACTGC | 51366 |
rs141801770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102370323 | AAGCACACGCCACCA[C/T]GCCTGGCTAATTTTT | 51366 |
rs141839787 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102368450 | TTCCCAAGGGGCACA[A/G]TCCTGCTCTGTCACC | 51366 |
rs141844819 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UBR5 | GRCh38.p7 | 8:102365337 | GGGTGTGGTGGTGCA[C/T]GTCTGTAGTCCCAGC | 51366 |
rs141856791 | snp | A/G | 3.2962e-05 | 0.00405954 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102360133 | AAACCATGGAGAGTC[A/G]CTTGTCCTACCAGGC | 51366 |
rs141885384 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102268556 | AAAGGGATATGTAAT[A/C]TGTTAGATATTTTTT | 51366 |
rs141886654 | snp | C/T | 0.000181206 | 0.00951683 | missense, nc-transcript-variant, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102277102 | TTTCTTCTGGCAGCA[C/T]GGGCTGTTCTTCCCC | 51366 |
rs141888290 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | UBR5 | GRCh38.p7 | 8:102362129 | TTGAACAAACCAGAT[C/T]ATCAATGTCCTTATC | 51366 |
rs141926093 | snp | A/G | 0.000734446 | 0.019149 | intron-variant | UBR5 | GRCh38.p7 | 8:102285784 | CCCGCTGAACTTGCT[A/G]TAAGGAAAAAGGACA | 51366 |
rs141968463 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102305976 | GGCTCAAGTGATGCC[C/T]CCACCTCAGCCTCCC | 51366 |
rs141973664 | snp | A/G | 0.000594815 | 0.0172352 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285597 | ATACTTAGGAATAAG[A/G]CCCATCAAGTCCGAG | 51366 |
rs141998967 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102354934 | AGGAGTTAAAGACCA[C/G]CCTGGGCAACATGGC | 51366 |
rs142033197 | snp | A/G | 3.29565e-05 | 0.00405921 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102305275 | GTCACAGCGCAGAAT[A/G]TGTTGCATTAAGGTT | 51366 |
rs142061217 | snp | C/T | 0.000298611 | 0.0122154 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102265257 | CACTTCGACTAGAGC[C/T]ATGGCGCTTTCGGTT | 51366 |
rs142088871 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBR5 | GRCh38.p7 | 8:102402087 | CAGGTGTGGTGGCAC[A/G]CACCTGTAGTCCCAG | 51366 |
rs142104351 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | UBR5 | GRCh38.p7 | 8:102282012 | TGTCTCTACTAAAAA[C/T]ACAAAAATTAGCTGG | 51366 |
rs142108273 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102317279 | GGAAATGGCACACCA[G/T]GAGATTATATCCCTC | 51366 |
rs142112005 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102388491 | AGCTTACTAATTAAA[C/T]GGATGATGAAGCCGA | 51366 |
rs142115753 | snp | C/G | 0.00369524 | 0.0428248 | intron-variant | UBR5 | GRCh38.p7 | 8:102297646 | TCATCTTTCAGGAAA[C/G]GACTTAATTAGCCAT | 51366 |
rs142131013 | snp | C/T | 0.0026528 | 0.036323 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295526 | GAATAGTAAGAGGTG[C/T]TCTCCCCTGCAAAAC | 51366 |
rs142150797 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | UBR5 | GRCh38.p7 | 8:102385539 | TCTTGACTCTGTTTT[G/T]TTTTTTTTTTTGAGA | 51366 |
rs142152663 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBR5 | GRCh38.p7 | 8:102291825 | CAAGGTAAGTCCAGC[A/G]TCTAAACTTTAATTA | 51366 |
rs142175912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102351867 | GCGCCTACAGTCCCA[A/G]CTACTTAGAAGGCTG | 51366 |
rs142211536 | in-del | -/TG/TGTG | 0.329783 | 0.236927 | intron-variant | UBR5 | GRCh38.p7 | 8:102309037 | TAGATAGCTACACAA[-/TG/TGTG]TGTGTGTGTGTGTGT | 51366 |
rs142219176 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102290378 | CAAACAAACAGATAA[A/G]TAGTCTCAATATGAT | 51366 |
rs142247872 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102341224 | AGAGAAATAGGAAAC[A/G]GTAATTGATGTACAA | 51366 |
rs142259387 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B, nc-transcript-variant | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102251938 | TGAATCTTACAACAT[A/G]CAGAAGCATGGAAAC | 51366 |
rs142280664 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102389099 | TATCACTATTCTTAA[C/T]GATCACAGTGGTTTA | 51366 |
rs142326724 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBR5 | GRCh38.p7 | 8:102399887 | GGAGGTGGGGGTTGC[A/G]GTGAGCCGAGATGGC | 51366 |
rs142373047 | snp | C/G/T | 0.0170251 | 0.090679 | intron-variant | UBR5 | GRCh38.p7 | 8:102382166 | ATGCCACACCTGCCA[C/G/T]GGGTCCAATTCAATT | 51366 |
rs142399805 | in-del | -/AAAATG | | | utr-variant-3-prime, cds-indel, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102253887 | ACCATAAAAAAAGTT[-/AAAATG]AAAACACAGAACATA | 51366 |
rs142452758 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102324154 | AGAAGAAACTAAAAG[G/T]CATTATAATTTAAAA | 51366 |
rs142465100 | in-del | -/A | 0.0930568 | 0.194599 | intron-variant | UBR5 | GRCh38.p7 | 8:102274857 | TTTTTTAAAAAGAAC[-/A]AAAAAAATGCATTCC | 51366 |
rs142473006 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102338179 | GAGGGGAAGCAAGAA[A/T]GGATAGATTTTAGGG | 51366 |
rs142475010 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | UBR5 | GRCh38.p7 | 8:102375600 | GTTACTCAATACTTC[A/G]TAGTTGTGGGATACT | 51366 |
rs142497309 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102273313 | AGTTAAATATAACTA[A/T]CCTAACTATATGAAA | 51366 |
rs142504813 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | UBR5 | GRCh38.p7 | 8:102365030 | ATACAATGTTTACGA[C/T]AGGCAGTATTAACAA | 51366 |
rs142513614 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102312722 | GTGATTACAGTCAGT[A/G]AATGTTTTCAGTAAT | 51366 |
rs142528208 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBR5 | GRCh38.p7 | 8:102274342 | TTCTAAGACTGCTAC[C/T]GTGTATGTTGTGGCA | 51366 |
rs142560455 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102364506 | AAATGCTTATGAATA[C/T]ATGAAAAGCAAGTGT | 51366 |
rs142570052 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102271744 | AGACTTCCCAGTTTC[C/T]TCATTCACATCTCCT | 51366 |
rs142570228 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102409414 | TTTTTAAGAGGATGT[A/G]GGTAAAGAAAGAAAA | 51366 |
rs142572126 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBR5 | GRCh38.p7 | 8:102362764 | AGTCAGCTGTTCTAT[A/G]ACTTTATCCTATAAG | 51366 |
rs142583001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102359895 | TAGCCTGTGTGAGTT[A/G]TTTTTATCATGGTGG | 51366 |
rs142585966 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102267635 | AGAGAAGAAAAGAGC[A/T]TCAGCAAAGAAAATA | 51366 |
rs142597673 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102259193 | TTTATATTATTAAAG[C/T]ACAAGACATAATTTT | 51366 |
rs142618507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102307859 | CCTGTGGATGTTCCT[C/T]CTCGATCTCTTATGC | 51366 |
rs142622059 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | UBR5 | GRCh38.p7 | 8:102403171 | CCCAGCATTTTGGGA[A/G]GCCAAGGTGGGAAGA | 51366 |
rs142623692 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102393577 | GGAGGTGGAGGTTGC[A/T]ATGAGCTGAGATCAC | 51366 |
rs142678454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102327467 | AAATACCCCAAATGT[C/T]AACTGTAGTTATCTC | 51366 |
rs142703972 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102378473 | ACATGGTGAAATCCC[A/G]TCTCTACTAAAAATA | 51366 |
rs142750931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102374970 | GGGAGCTTAACAAAC[A/G]GACATTCATGTCTTA | 51366 |
rs142761797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102292785 | TATGGGAGAGCTCTG[C/T]CAGACAAAACTGGAT | 51366 |
rs142805335 | snp | A/G | 0.00609138 | 0.0548506 | intron-variant | UBR5 | GRCh38.p7 | 8:102346405 | TTGGGCCTGAAATAA[A/G]AAATAAAAAGAAGTG | 51366 |
rs142816228 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102273866 | ATACATATGCTTATA[G/T]GTTTTAAAAGGGAGG | 51366 |
rs142928619 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | UBR5 | GRCh38.p7 | 8:102344387 | GGTACCACCTCAGCT[C/T]ACTGCAAGCTCTTCC | 51366 |
rs142960886 | snp | A/C | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102306721 | GTTTCAAGTAACAGC[A/C]AATTATTTAGTTAGA | 51366 |
rs142968444 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102337743 | TTCTTTTCCTCTGGC[A/G]TCTTTGTCTGGCTTA | 51366 |
rs142968475 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | UBR5 | GRCh38.p7 | 8:102391730 | ATGTCAGAAGCATTC[A/T]AACCACAGCAAATCC | 51366 |
rs143012925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102356083 | AGAGAAATGGGTTAT[A/G]AACTGGAGAATAAAA | 51366 |
rs143038207 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | UBR5 | GRCh38.p7 | 8:102390803 | ATCTGCAAAATGAAG[C/T]TGCGAATCTTGCAAA | 51366 |
rs143060208 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102388570 | ATAACAAGATTTGAG[A/G]GTGGCACATCTCACA | 51366 |
rs143097830 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102351507 | AGAATTGGTGGCTGC[C/T]AGGGACTAGAGGGAG | 51366 |
rs143098941 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | UBR5 | GRCh38.p7 | 8:102260041 | TAAAAAAAAAAATAT[A/T]TTTTTTTACCCTGGA | 51366 |
rs143124130 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102268979 | ATTGTACACATTACC[A/G]TCCATGTGCAATAAT | 51366 |
rs143182767 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102358078 | TTGAACCCGGGAGGC[A/G]GAGGTTGCAGTTAGT | 51366 |
rs143201926 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBR5 | GRCh38.p7 | 8:102341373 | AGTTTGGCAGTTGCC[A/G]AAGAAAACAGAATAA | 51366 |
rs143204040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102254586 | AAAGCCCTATTGTTA[C/T]GTTAATAACCTAAAA | 51366 |
rs143245775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102315132 | TTTATCTAGAAATAA[C/T]GAAATTTACACTTAA | 51366 |
rs143268985 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102366407 | CTCTAAGCAAAGACA[A/G]AATACAACTTGCCAA | 51366 |
rs143290364 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | UBR5 | GRCh38.p7 | 8:102310407 | GCTGGAGTTCAGTGG[C/T]GCGATCTCGGCTCAC | 51366 |
rs143354723 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102310223 | ACCAAGCTTTACAGG[C/T]TCTAGTTTCTTAAGA | 51366 |
rs143374248 | snp | C/T | 0.00013188 | 0.00811929 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102272680 | GACTTTTACTCTGTG[C/T]ACAGCCATTGGTGTA | 51366 |
rs143377111 | in-del | -/TA | 0.159292 | 0.232964 | intron-variant | UBR5 | GRCh38.p7 | 8:102314973 | ACATTTTTATTAAAC[-/TA]TGTATTTATATTAAT | 51366 |
rs143383894 | in-del | -/TTAA | 0.0577344 | 0.159793 | intron-variant | UBR5 | GRCh38.p7 | 8:102301197 | AATTGCAATTATTAT[-/TTAA]TTGAGGATAAATGTG | 51366 |
rs143390287 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102279703 | AATAGTAAGTCAGCA[C/T]ACTAGCACCAAATCT | 51366 |
rs143416987 | in-del | -/AG | 0.00755907 | 0.0610114 | intron-variant | UBR5 | GRCh38.p7 | 8:102403702 | TGTTTGTTTTGAGAC[-/AG]AGTCTCACTCTGTTG | 51366 |
rs143428328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102332553 | TCATGGTTCCTCAAA[C/T]ACATCATGACCTTTT | 51366 |
rs143458216 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | UBR5 | GRCh38.p7 | 8:102349601 | GAAGGGAGAGAGAGC[C/G]AAGTGGAGAGGAGAA | 51366 |
rs143483663 | snp | A/C/T | 0.000249816 | 0.0111738 | intron-variant | UBR5 | GRCh38.p7 | 8:102312294 | TCCATAATAAACTCA[A/C/T]GGAGTCAGTTCCAAT | 51366 |
rs143510452 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | UBR5 | GRCh38.p7 | 8:102363731 | GAAAAATAATTGTCA[A/G]GGCCTTTTTCAAAAC | 51366 |
rs143519707 | snp | A/G | 0.176861 | 0.239062 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102411653 | CCCCGGGATCCCCAG[A/G]TCCAGACCACCCCAC | 51366 |
rs143521748 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102328780 | TTTTAGTAGAGATGG[A/G]GTTTTGTATTTTTAG | 51366 |
rs143552597 | snp | A/G | 9.92146e-05 | 0.00704254 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102281296 | ATGGATACCTTTTGC[A/G]TTCTAGTTGAGGTGT | 51366 |
rs143611160 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102334387 | ACCTCCGCCTCCTGC[A/G]TTCCAGCGATTCTCC | 51366 |
rs143616705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102296653 | CCTAGTTACAATGTA[C/T]AATCACCTACTTTTA | 51366 |
rs143669015 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102268395 | TTTTAGTAGAGATAC[A/G]GTTTCACCATGTTGG | 51366 |
rs143692917 | snp | A/G | 0.0103356 | 0.0711407 | intron-variant | UBR5 | GRCh38.p7 | 8:102404214 | CAGTACTTTAGCTGT[A/G]CAAGTAACATAAATT | 51366 |
rs143697496 | in-del | -/TCC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102310770 | TTCACTGGCTTATAA[-/TCC]TCCTCCTCCTCCTCG | 51366 |
rs143703669 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102283855 | AAATGATGCCCCTGC[C/T]ACTTAATCCCTCAAC | 51366 |
rs143719892 | snp | G/T | 0.000197824 | 0.00994348 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102360605 | CATCATTATTATCAG[G/T]TTTACCCAATTCCAA | 51366 |
rs143723314 | snp | C/T | 4.94507e-05 | 0.00497221 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102360111 | CTAGAGTCTCAGAAC[C/T]TGAGAGAAACCATGG | 51366 |
rs143729042 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | UBR5 | GRCh38.p7 | 8:102334724 | AACACGGTGAAACCC[C/G]GTCTCTACCAAAAAT | 51366 |
rs143775454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102353667 | TGTAACACATGTACC[A/G]TACTAACATTAGATT | 51366 |
rs143796468 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | UBR5 | GRCh38.p7 | 8:102399716 | CTTTGGGAGGCCAAA[A/G]CGGGTGGATCACGAG | 51366 |
rs143820445 | snp | C/T | 0.00110318 | 0.02346 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102305194 | GAATGTCTGCAGCAT[C/T]TGTAGATTCTGCTCT | 51366 |
rs143842614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102397336 | GAGGGCAGAGGCCAG[C/T]CATCTTTGTATTCCA | 51366 |
rs143859050 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102316950 | TATGAGGGGGGAGGA[C/G]CCAAGATGGCCAAAT | 51366 |
rs143896177 | snp | C/G/T | 0.0228947 | 0.104514 | intron-variant | UBR5 | GRCh38.p7 | 8:102286792 | TTTCAAGCCCAGCTC[C/G/T]GTGGCTCAGGCAGGA | 51366 |
rs143911232 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | UBR5 | GRCh38.p7 | 8:102392723 | AAAAAGACAGGATTC[C/T]GCTTAGTTTTGAAGT | 51366 |
rs143915591 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102332903 | CACACTGACCAACTG[C/T]TGAATGAACAAATGA | 51366 |
rs143935553 | in-del | -/AA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102371276 | ATATCCTTTTTTTTT[-/AA]AAAAAAAAAAAAAAA | 51366 |
rs143937619 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102369304 | ACCAAAACTCAGCAA[A/G]TGATTTCTTAAAGGT | 51366 |
rs143971650 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102262162 | GATAAAGAATTTTAT[C/G]TAATTTGAAGATACA | 51366 |
rs144001032 | snp | C/T | 0 | 0 | intron-variant | UBR5 | GRCh38.p7 | 8:102398737 | AGTGAGGCGAGATCG[C/T]GCCACTGCACTCTAG | 51366 |
rs144019892 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | UBR5 | GRCh38.p7 | 8:102397663 | CCGAGATTGCCATTG[C/T]ACTCCACCCTGGGCT | 51366 |
rs144052464 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBR5 | GRCh38.p7 | 8:102274664 | CTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC | 51366 |
rs144071860 | in-del | -/AC | 0.0232847 | 0.105357 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102414277 | GTCTGTTAATGAATT[-/AC]ACACACACACACACA | 51366 |
rs144076272 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102263471 | AAATATTTTTAGGAA[C/T]GTGGGTAGTTTTCTT | 51366 |
rs144139021 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102264625 | TCCCCCCACACATAA[A/T]ACGTATTAATATTTT | 51366 |
rs144154804 | snp | C/G/T | 4.94909e-05 | 0.00497428 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102262002 | ATCTGAACTCTGAGA[C/G/T]GCGAGGATTAGTTGC | 51366 |
rs144168456 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102401556 | CAAAATCAGTCCACA[C/T]GTCATCTCTGACCTG | 51366 |
rs144198486 | in-del | -/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102362665 | TTTAGGGCTTAAAAA[-/C]CTGCCACAAAGCATA | 51366 |
rs144248785 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102300058 | TATGGGGGGTGAAAC[C/T]GGATCCTGGTGGTCA | 51366 |
rs144306273 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102307791 | AACATCCTGCTTGAC[A/G]TGTGCTCTTCATTTG | 51366 |
rs144313877 | snp | A/C | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102313834 | ATTCTTGACATCTTC[A/C]ACAAAAACCACTTCC | 51366 |
rs144344248 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102369776 | TTCATCAAGGACACT[A/T]TGAAGTGAAACTGGC | 51366 |
rs144416311 | snp | C/T | 0.00414215 | 0.0453202 | intron-variant | UBR5 | GRCh38.p7 | 8:102298532 | ATATTAATTACTACT[C/T]ATTTTCCTTCCTGAT | 51366 |
rs144432944 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102363733 | AAAATAATTGTCAAG[A/G]CCTTTTTCAAAACCG | 51366 |
rs144469342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102285442 | ACATTTAATTCCCCT[A/G]ATACTGGAATTCTCA | 51366 |
rs144493276 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102333923 | TTCATTTTGTTCTTA[C/G]TTCATATTAAATTAC | 51366 |
rs144540525 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102357219 | ACTTGAGTTTAATCA[C/T]GAGAAATGATAAACA | 51366 |
rs144547260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102386699 | TTAGTTCATATAGGC[C/T]GGGCGCGGTGGCTCA | 51366 |
rs144547325 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102330919 | TTCAGCCTCTGCCAT[C/G]CTTGAGACAGCAAAA | 51366 |
rs144558624 | in-del | -/C | | | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102411166 | AAATCCAAACCAAAA[-/C]CAGCCTATAAAAGAC | 51366 |
rs144579862 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102279663 | TTTGCTAAGCAGAGT[A/G]ATGTCTGAGCAATTT | 51366 |
rs144616449 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102304760 | CTACATTCTAAAAAT[G/T]TAGATAAAAGTTGCC | 51366 |
rs144621399 | in-del | -/T | 0.0260105 | 0.111035 | intron-variant | UBR5 | GRCh38.p7 | 8:102287641 | TAAGCCAGAATATCG[-/T]TAAGGGTGGGAACTA | 51366 |
rs144623404 | snp | C/G/T | 0.00031317 | 0.01251 | synonymous-codon, missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311813 | AGGAAAATTATTTTC[C/G/T]TGTTCTGCTTTTCCT | 51366 |
rs144630551 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102300687 | CAAAAAAATTTTTAA[C/T]AGTACAACTTGCATC | 51366 |
rs144633311 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102352861 | CACTCAAATTCTTTT[C/G]TATAAGCACTGCTGA | 51366 |
rs144636920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102297121 | GAAAACTAGAACTTA[C/T]AAAGGGCTACAGCAA | 51366 |
rs144670403 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102392273 | GGACTGCTCTGCCTA[C/T]GGAGTAGCCATTCTC | 51366 |
rs144715022 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102350621 | TAGAAGGAAACATAA[A/G]GGAAAAGCTTCATGG | 51366 |
rs144719407 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | UBR5 | GRCh38.p7 | 8:102294176 | AGATGTTTAGACATT[A/C]ATAAAGTTATAAGTT | 51366 |
rs144758602 | snp | A/G | 0.105924 | 0.204309 | intron-variant | UBR5 | GRCh38.p7 | 8:102261478 | GAGGCCAAGGTGGGT[A/G]GATCATGAGGTCAGG | 51366 |
rs144773332 | snp | A/G | 4.94417e-05 | 0.00497176 | missense, nc-transcript-variant, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102276978 | AGCAAATACCTGAAA[A/G]ATGTGAGAGGTGGCC | 51366 |
rs144774001 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102299411 | AAGTGTGTCCTTTTT[-/T]CTTCCAGATGACTAG | 51366 |
rs144791170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102276423 | TCTAAAGCCAACATT[C/T]TGCCTCAGCATCTTT | 51366 |
rs144847208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102409860 | CCACAAATCAGCTAC[C/T]TCAAAACTTAGGATA | 51366 |
rs144848171 | snp | A/G | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102414094 | CCCGGGCAACAGAAC[A/G]AGACTCCATCTCAAA | 51366 |
rs144863935 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBR5 | GRCh38.p7 | 8:102257326 | GGATTAAGGATGTAT[A/G]CAGGGAGAAGCATAT | 51366 |
rs144865093 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102345776 | CGTTAAGATATAACA[C/T]TTGTGGCCGGGCACG | 51366 |
rs144886259 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102407269 | TGAGTAGCTGGGATT[A/G]CAGGCGTCCACCACC | 51366 |
rs144969307 | in-del | -/TT | 0.498734 | 0.0251279 | intron-variant | UBR5 | GRCh38.p7 | 8:102335201 | CTTATATGTGAAGTC[-/TT]TTTTTTTTTTTAAAG | 51366 |
rs145007980 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102278014 | AAAATAAAATTAAAT[A/G]AATAAATAAATAAAT | 51366 |
rs145010088 | in-del | -/TAT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102337710 | ATCAATGTTCAAAGA[-/TAT]TATTAGCCTATGGTT | 51366 |
rs145032045 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | UBR5 | GRCh38.p7 | 8:102331304 | GTACACAGCACAGAG[A/C]CCAGTGCAAATAAGC | 51366 |
rs145039781 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102276308 | GTAACATCTCTTTCC[C/T]TAATGCCCTGACTTA | 51366 |
rs145062267 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102253765 | AACCGCAATAAAAGT[A/G]GTTTTTATAGGTAAA | 51366 |
rs145079204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102325799 | TCAAAAAAATAGTGG[C/T]GAGAAAAGTAACATC | 51366 |
rs145081370 | snp | C/G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102409004 | TCTCCCCTCAAGCTC[C/G/T]ACGAACCACATTCTT | 51366 |
rs145097554 | snp | C/T | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102305249 | ATTAGATATTGTCGA[C/T]AGGCCTCATAGTCAC | 51366 |
rs145098295 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102390611 | TGCATAAGGAAACAA[A/C]AGTTGACAAAGCCAA | 51366 |
rs145100120 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303790 | CTAGGAAGCAAGAAT[A/G]ATGAATTTAGAACAA | 51366 |
rs145127545 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | UBR5 | GRCh38.p7 | 8:102272859 | ACAATCTGAAAATCT[A/T]GTTTTAGCCTTTCCT | 51366 |
rs145137858 | snp | C/T | 0.000412769 | 0.0143602 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285165 | GCTAGCTTCTTCTCG[C/T]GCAGTCATCCTCTCT | 51366 |
rs145166702 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | UBR5 | GRCh38.p7 | 8:102323692 | TGTTTCTAGGCCAGG[A/C]GTGGTGGCTCACGCC | 51366 |
rs145192351 | in-del | -/CCT | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102307384 | ACCTCTGTATCATCA[-/CCT]CCTTTAGTTTGAAAC | 51366 |
rs145213588 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102408731 | AGTTGAGGGGAAAAC[A/G]GAATCAAAACACTAA | 51366 |
rs145232595 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102289245 | CCTTAAAGACAAGTT[C/T]GTGTCCAATTTCCTA | 51366 |
rs145248941 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | UBR5 | GRCh38.p7 | 8:102339267 | AGGCACGGTGGTCAC[A/G]CCTGTAATCTCAGCA | 51366 |
rs145249347 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBR5 | GRCh38.p7 | 8:102259900 | GGGCATGCTGGCGCG[C/T]GCCTATAGTCCCAGC | 51366 |
rs145250341 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102340617 | TTCCCTTTAATAGCT[C/G]TCTACATTCTCTTGT | 51366 |
rs145271737 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | UBR5 | GRCh38.p7 | 8:102390259 | GGCATGGTGGCTCAC[A/G]CCTGTAATCCCAGTA | 51366 |
rs145309458 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | UBR5 | GRCh38.p7 | 8:102395338 | CTGACAGGCAGCAGA[C/T]GCCCCCAAATCTTGC | 51366 |
rs145336410 | snp | A/T | 0.0505692 | 0.150756 | intron-variant | UBR5 | GRCh38.p7 | 8:102256110 | AAATCGAGATCATCC[A/T]GGCTAACATGGTGAA | 51366 |
rs145337261 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | UBR5 | GRCh38.p7 | 8:102359531 | ACATCATTTACAAAC[C/T]TCATTAAACTGATTC | 51366 |
rs145353927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102257969 | ACTGATATTCACATG[A/G]GTTTTATCTCATCTG | 51366 |
rs145391465 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102282219 | ATACATTGGAATTTA[C/T]GAAAATTAAAATTGT | 51366 |
rs145392211 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102375215 | AAAATACAAAAATTA[G/T]TCAGGGGTGGTGGTG | 51366 |
rs145422859 | snp | C/T | 1.64939e-05 | 0.0028717 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102326563 | GGGTACCAACAGTGA[C/T]GTTCGGCATTGAAGA | 51366 |
rs145443792 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, downstream-variant-500B | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102252577 | CACATTGATGCTAAT[C/T]AGCTCTTGATCTAAT | 51366 |
rs145443902 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102307691 | ATCCCCACTATCAAT[A/G]ATGACCTAGATGGAG | 51366 |
rs145454925 | snp | C/T | 0.000116894 | 0.00764416 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102304165 | TCTTTCAGAACGCTC[C/T]GCTTCTGAAAAATGA | 51366 |
rs145476648 | in-del | -/G | 0.0437281 | 0.141251 | intron-variant | UBR5 | GRCh38.p7 | 8:102267834 | TCAAAGTTTCAAACT[-/G]GGGTATCAGATTAGC | 51366 |
rs145481406 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102301939 | AAATTTTAACATTGC[A/G]CAGGCCAAACAAAAA | 51366 |
rs145483504 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102389234 | ATGAGGCAGAAGTGA[C/T]GCTGCAAAACTTCTA | 51366 |
rs145538962 | in-del | -/ATATT | 0.0422008 | 0.138995 | intron-variant | UBR5 | GRCh38.p7 | 8:102335388 | TAATAAAATGGTATC[-/ATATT]ATGGATTTTTGTTAA | 51366 |
rs145561090 | snp | C/T | 0.000268173 | 0.0115765 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285129 | AAGAATTTCATACCG[C/T]CTGCCTTCAAGTGTT | 51366 |
rs145575877 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102402826 | CTTGAAACGGCAGGT[G/T]CTCGACACTTCTATA | 51366 |
rs145577823 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | UBR5 | GRCh38.p7 | 8:102317362 | CTCTGAGATCAAACC[A/G]CAAGGCGGCAGCCAG | 51366 |
rs145582275 | in-del | -/A | 0.462034 | 0.132445 | intron-variant | UBR5 | GRCh38.p7 | 8:102392608 | GGACTATTAGATACC[-/A]AAAAAAAAAAAAAAC | 51366 |
rs145637985 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102348966 | AAACCTAGAAAAGCT[A/G]TTGTCATCCTTTTGA | 51366 |
rs145651567 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102325256 | AAATAGTGGGTAAAC[A/G]CTGAAAGTTTTCTGG | 51366 |
rs145670915 | snp | C/T | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311376 | TTAAAGAATGCACAC[C/T]CATTCCAAGACTACT | 51366 |
rs145742638 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102334604 | GCCAGTTAATGTTAA[G/T]TAACAGTACCGAGTC | 51366 |
rs145766816 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102387149 | GTAACAATGCTAAAT[A/G]TAACACTTAAAATGT | 51366 |
rs145806768 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBR5 | GRCh38.p7 | 8:102276562 | TCCATATTGCTTCTA[A/G]GAAGCTTGGGCCACT | 51366 |
rs145811106 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UBR5 | GRCh38.p7 | 8:102399255 | AATTTAAATCACTAC[A/G]TAATATATATTATCT | 51366 |
rs145830552 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102414668 | CCTCCCGAGTAGCTG[A/G]GATTACAGGCGCTGC | 51366 |
rs145842676 | in-del | -/CAG | 0.101658 | 0.201233 | intron-variant | UBR5 | GRCh38.p7 | 8:102312973 | AAACAGCCACATATA[-/CAG]CTAGTGGCTACAATA | 51366 |
rs145937077 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBR5 | GRCh38.p7 | 8:102401660 | ATCCTACCAGGAATC[A/G]TCTCAGGTAGCAGGA | 51366 |
rs145982879 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | UBR5 | GRCh38.p7 | 8:102291562 | AGTGAAACAGAAAAA[G/T]CATACCTCGAGAGAT | 51366 |
rs145992568 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102367937 | TCTCTTCATCTGTGT[A/G]TGAAAAACTTGCTCA | 51366 |
rs146015475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102271912 | TCTGCTCCTACTTGA[C/T]GTGAATCTCCTAAGG | 51366 |
rs146040983 | snp | A/G | 1.64784e-05 | 0.00287035 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102281352 | GCCTTAATCCAGTAT[A/G]TAAGTGCTTGAAAAA | 51366 |
rs146079473 | snp | C/T | 0.000307953 | 0.0124049 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102277106 | TTCTGGCAGCACGGG[C/T]TGTTCTTCCCCTTCT | 51366 |
rs146096321 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102294016 | CTCTTGCCACTGAAC[A/G]TAGAAACCTCATTGT | 51366 |
rs146117297 | snp | C/T | 3.45764e-05 | 0.00415776 | intron-variant | UBR5 | GRCh38.p7 | 8:102285801 | AAGGAAAAAGGACAA[C/T]CACAATGAGCTAATG | 51366 |
rs146238984 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | UBR5 | GRCh38.p7 | 8:102405626 | GAGTTCAAGACCAGC[A/G]TGATCAACACGGTGA | 51366 |
rs146248859 | snp | C/T | 0.021333 | 0.101051 | intron-variant | UBR5 | GRCh38.p7 | 8:102264261 | ACTCTGCTATGCCAT[C/T]TCCCCATAGTCTTTT | 51366 |
rs146259530 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102316209 | CACTTTTAACACTGA[C/G]GAATTACAGCAGTAA | 51366 |
rs146264509 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102401462 | ACAGTACTGACTCCT[A/G]TCTCTGCAGGCAAGT | 51366 |
rs146268222 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102378061 | TCAATGCACTCTAAT[A/G]GGTCTCTAATCTAGA | 51366 |
rs146276613 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102398542 | AATCCCAGCACTTTG[A/G]GAGGCCAAGGAGGCT | 51366 |
rs146296345 | in-del | -/CAT | 0.0640965 | 0.167152 | intron-variant | UBR5 | GRCh38.p7 | 8:102325811 | TGGCGAGAAAAGTAA[-/CAT]CATTTACATTTTAGC | 51366 |
rs146301145 | snp | C/T | 8.29497e-05 | 0.00643956 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295263 | GGCATTCCAGTCCTG[C/T]AGAACACGCTCCAAT | 51366 |
rs146357523 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBR5 | GRCh38.p7 | 8:102388504 | AACGGATGATGAAGC[C/T]GAGTGGTTCTTCTTT | 51366 |
rs146358480 | snp | A/G | 0.222333 | 0.248464 | intron-variant | UBR5 | GRCh38.p7 | 8:102319961 | agagggaaatttaga[A/G]cactaaatgcccaca | 51366 |
rs146369459 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102297796 | ATATAAAGTAAAGCA[C/T]AATTACATCATACCC | 51366 |
rs146383134 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102386031 | CTAATATGATGTGCA[C/T]AGTCCACCATCTCAC | 51366 |
rs146418789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102262174 | TATCTAATTTGAAGA[C/T]ACATTGATATAGAAT | 51366 |
rs146431484 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBR5 | GRCh38.p7 | 8:102398738 | GTGAGGCGAGATCGC[A/G]CCACTGCACTCTAGC | 51366 |
rs146458599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102395733 | TCTATTCAGCAGTGT[C/T]AAGTCACAAGGTAAT | 51366 |
rs146518270 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | UBR5 | GRCh38.p7 | 8:102357874 | GAGTAGGCTGGGTGC[A/G]GTGGCTCAGGCCTGT | 51366 |
rs146529056 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | UBR5 | GRCh38.p7 | 8:102264650 | TATTTTGAGAAATTC[A/T]CTACAGCCTCCTTTC | 51366 |
rs146545078 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102331116 | TATAAATACAGTATA[G/T]ACTACATATAACATA | 51366 |
rs146545530 | snp | C/T | 1.65971e-05 | 0.00288067 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102261243 | GGTATATTTACACCA[C/T]TAGGAATGAGTTCAA | 51366 |
rs146578894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102375899 | GATCACTGGAGGTCT[C/T]CCAATGGCAAGTAAT | 51366 |
rs146580551 | in-del | -/AAAGACCTTAATGGTA | 0.0836354 | 0.186609 | intron-variant | UBR5 | GRCh38.p7 | 8:102331001 | GAAGATAATGAGAAT[-/AAAGACCTTAATGGTA]ATCCGCTTCCACTTA | 51366 |
rs146599651 | in-del | -/AACT | 0.0648419 | 0.167978 | intron-variant | UBR5 | GRCh38.p7 | 8:102305545 | ATTTTTAGCTTTCTC[-/AACT]AACTCAGCTCTGCAA | 51366 |
rs146637832 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102334143 | AAGAGCTTAAACAAG[G/T]GGTCAAATGAAATGG | 51366 |
rs146659305 | snp | C/T | 0.159951 | 0.233219 | intron-variant | UBR5 | GRCh38.p7 | 8:102309094 | GTCTCACTCTGTCGC[C/T]CAGGCTGGAGTGCAG | 51366 |
rs146665531 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBR5 | GRCh38.p7 | 8:102395060 | CTTCTGCCTAGGGAG[C/T]TCTTCCAGTTCTTAA | 51366 |
rs146713185 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102374327 | AACTTGAGGATCCAG[A/G]GAATGAAAGCTAAGT | 51366 |
rs146742588 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102261832 | CTCTTTCATTCCCTA[A/G]CTAAACTGTCTATAC | 51366 |
rs146768756 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBR5 | GRCh38.p7 | 8:102259897 | GCTGGGCATGCTGGC[A/G]CGCGCCTATAGTCCC | 51366 |
rs146771933 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBR5 | GRCh38.p7 | 8:102273438 | TTAACAACTGCTGGC[A/G]AGACTGAGCAATCAG | 51366 |
rs146780475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102283441 | CATTATGATGAAGGG[C/T]TGAAAAACTATGGAA | 51366 |
rs146784093 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | UBR5 | GRCh38.p7 | 8:102375700 | CTGGGCTGGTGTTAG[C/G]GAAATGTGCTACAGG | 51366 |
rs146784501 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102358875 | AACTTCCTGGGCTTA[A/G]ATGATCCTCCCACCT | 51366 |
rs146785335 | in-del | -/TT | 0.00438332 | 0.0466095 | intron-variant | UBR5 | GRCh38.p7 | 8:102382386 | TCAGGAAGCCTAAAC[-/TT]CAGGAAAAAAGGAAA | 51366 |
rs146878598 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | UBR5 | GRCh38.p7 | 8:102380954 | ATTCATTCATAGTTC[C/T]ACATGGCTGGGGAAG | 51366 |
rs146902228 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102267854 | ATCAGATTAGCCCCA[C/G]GATAGAAACTACAGC | 51366 |
rs146909587 | snp | A/G | 1.64876e-05 | 0.00287116 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102272693 | TGTACAGCCATTGGT[A/G]TAGTAGCACATCTTC | 51366 |
rs146914625 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102355113 | AGCCTGGGCAACAGA[C/G]GGAGATCCTGTCTCT | 51366 |
rs146914716 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102403515 | CACATCACTACACTC[C/T]AGCCTGGGCAATAGC | 51366 |
rs146925103 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UBR5 | GRCh38.p7 | 8:102384277 | ACAGCAATGATTCTC[A/G]TCTTTTCTTCAAAGG | 51366 |
rs146940222 | in-del | -/G | 0.0422008 | 0.138995 | intron-variant | UBR5 | GRCh38.p7 | 8:102336820 | TTGCTTTCACTATTT[-/G]GGGTATTTTATGGTT | 51366 |
rs146959929 | in-del | -/TAGTGCTTCCAGTAC | 0.0279526 | 0.114869 | intron-variant | UBR5 | GRCh38.p7 | 8:102337291 | TTGTTTGATGTTCAT[-/TAGTGCTTCCAGTAC]TATGCTGAATGGAAT | 51366 |
rs146966075 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102267268 | GAATGTGGTCTTCAT[A/G]GGGGTGCTGGAACAC | 51366 |
rs146984336 | snp | G/T | 0.00795532 | 0.062565 | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102253104 | CTATGCCAAGTAAGG[G/T]GTCACACTTCACTTC | 51366 |
rs146997597 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102335523 | TGTAAACTTCAAATA[G/T]ACACAATAAAATTTA | 51366 |
rs147020418 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102388386 | ACAATGCCTGACACA[A/C]AGTAGGCACGCAAAC | 51366 |
rs147022462 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBR5 | GRCh38.p7 | 8:102332282 | TTTCCTTGAACAACT[A/G]TAGCATTCTCATAAC | 51366 |
rs147031102 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102361059 | ATAATGGAAGAGATA[A/C]AATGATGCACAATTC | 51366 |
rs147093777 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102263240 | TTGCAGTTTCCAAGA[A/T]CCTATTGACGACAAT | 51366 |
rs147103350 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102314619 | AAAAAACCAAAGTAA[C/T]AGAGATACAAATTAT | 51366 |
rs147144474 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102279973 | GAGTTGGGATATTTT[A/C]TCTTTTCATTGTATT | 51366 |
rs147154180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102276313 | ATCTCTTTCCCTAAT[A/G]CCCTGACTTAGACCA | 51366 |
rs147169480 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102412741 | TCCGCTCCGGAGCGG[C/T]GGGGGAGGGGCAAAC | 51366 |
rs147177313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102328960 | ATATACATTAGATTA[C/T]TAAGGCTTGAGACAC | 51366 |
rs147191332 | snp | C/T | 0.000281945 | 0.0118698 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102312201 | CTTTTTAGGAGTCCT[C/T]TGGAAACAGTCGGGA | 51366 |
rs147239131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102351255 | ATGTTCAAAGCAGCA[C/T]CATTCACAATTGCCA | 51366 |
rs147259517 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102258084 | TCTGCCTGTCTAAAA[C/T]GCTTTCAGATGATGC | 51366 |
rs147262205 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102397367 | GTGTATACACAGGTT[A/T]GCTGGCAAAGTATTT | 51366 |
rs147273353 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102392755 | CAAATTAATTTAATA[G/T]AGATATATGCTAATG | 51366 |
rs147333184 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBR5 | GRCh38.p7 | 8:102263688 | ACCCCCATGTACCTC[C/T]TATAGGTATTTTTGA | 51366 |
rs147348173 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102327668 | ACTTCTCATGTTGGT[A/G]TTCCACTACTCAAAG | 51366 |
rs147379758 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102374975 | CTTAACAAACGGACA[C/T]TCATGTCTTAGCTCT | 51366 |
rs147452415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102307289 | AATGTAAATCCTGTG[A/G]TTTTTCAATATTGGT | 51366 |
rs147494919 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102351652 | TGTATATACTTAAAA[A/G]TGCTTATAATGGTAA | 51366 |
rs147579985 | in-del | -/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102358770 | CAACCCTTTTCTTTT[-/C]TTTTTTTTTTTTTTT | 51366 |
rs147580661 | snp | C/T | 1.65436e-05 | 0.00287602 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285203 | CTGAATTCTGAGAAG[C/T]GTGAAGAGGATGATT | 51366 |
rs147596997 | snp | A/G | 6.62241e-05 | 0.00575392 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102297596 | CTCTTTTTCACTTGA[A/G]GATATTTCAGCTAAA | 51366 |
rs147599555 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102272962 | GCATACAAGAATGTC[C/T]TGCAAATTAAATCAG | 51366 |
rs147609731 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | UBR5 | GRCh38.p7 | 8:102290240 | TTATGAAACGGGGTA[A/G]AAGATGTTGAAGTCA | 51366 |
rs147610156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102348154 | TGAACCAGGACCCAG[A/G]AGGCAGAGGTAGCAG | 51366 |
rs147703355 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102252984 | TATTATGCCACTGAA[A/T]AAAGCTACTTAAACC | 51366 |
rs147713638 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102267505 | ATATACTCACAAAAA[C/T]CTTTTCACCAAAAAT | 51366 |
rs147713884 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | UBR5 | GRCh38.p7 | 8:102323837 | GGGCATGGTGGCATG[C/T]GCCTGTTATCCCAGC | 51366 |
rs147716436 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102407202 | GCAACCTCTGCCTCA[C/T]GGGCTCAAGCTCTGT | 51366 |
rs147725981 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102402871 | CCTGAACTCATGGGG[A/G]AGAAAATAAAAACTT | 51366 |
rs147799868 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102317299 | TTATATCCCTCACCT[A/G]GCTCAGAGGGTCCTA | 51366 |
rs147821381 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBR5 | GRCh38.p7 | 8:102389651 | TTGGGCCCTGGCTCC[A/G]TTGGTATATGACTAA | 51366 |
rs147840526 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102295860 | TGACATTATGAAGGT[A/G]TAACTCACTGAAACC | 51366 |
rs147914999 | snp | A/G | 0.0010938 | 0.0233603 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295329 | ATCTGGCATATCTGA[A/G]TCTAAAATGAAAAAG | 51366 |
rs147928148 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102370103 | AGTAATAATTCATTC[C/T]TCTTACTAAAACAGC | 51366 |
rs147928737 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102313695 | TACCACTGAAGATGA[C/T]AAATAAAACAGCCCT | 51366 |
rs147938122 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | UBR5 | GRCh38.p7 | 8:102365322 | ATTCAAAAATTAGCC[A/G]GGTGTGGTGGTGCAC | 51366 |
rs147946074 | in-del | -/GGAAGGAAGGAAGGAA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102387721 | AAAAAAAAAAAAAAT[-/GGAAGGAAGGAAGGAA]GGAAGGAAGGAAGGA | 51366 |
rs147980404 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | UBR5 | GRCh38.p7 | 8:102296681 | TTATTTAAGGAGGGC[A/G]ATGTTTGAACTAGCA | 51366 |
rs147992130 | in-del | -/ACACAC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102382826 | GAAAATCACATTAAA[-/ACACAC]ACACACACACACACA | 51366 |
rs148066830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102374075 | TCTATTAAATGCAGA[C/T]AGAACTACCACTTGT | 51366 |
rs148096616 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102362032 | GATTCTTGAGTGCAC[A/G]TGGATATCATGAAAT | 51366 |
rs148103121 | in-del | -/A | 0.26078 | 0.249767 | intron-variant | UBR5 | GRCh38.p7 | 8:102265520 | TAAAGTCATTTAATG[-/A]AAACTCGGATAAGCT | 51366 |
rs148105163 | snp | A/G | 0.00296242 | 0.0383723 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102360130 | GAGAAACCATGGAGA[A/G]TCGCTTGTCCTACCA | 51366 |
rs148105280 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBR5 | GRCh38.p7 | 8:102268405 | GATACGGTTTCACCA[C/T]GTTGGCTAGGCTGGT | 51366 |
rs148116258 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102284041 | CCCAGAGTAACAAAG[C/T]TGTTTATCCTGAGGT | 51366 |
rs148120190 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | UBR5 | GRCh38.p7 | 8:102404270 | AAATATTAATACCTT[C/T]TTTAATATCCTGACA | 51366 |
rs148139889 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102305872 | CCTCCCGCCTCAGCC[A/T]CCCATGTAGCTAGCA | 51366 |
rs148147371 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102354359 | CTGCTACAAACTGTC[C/T]TACCCACCTGAAGGG | 51366 |
rs148159249 | snp | A/T | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102305209 | CTGTAGATTCTGCTC[A/T]AAAACAACCGCTTGC | 51366 |
rs148188146 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | UBR5 | GRCh38.p7 | 8:102254850 | ATAAAGTGTCTATTA[C/G]TGGAAAAAAGGCTGC | 51366 |
rs148190327 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102341719 | GCAGTAAAAAACAAG[C/T]GAAAAACATGGGTTC | 51366 |
rs148247259 | in-del | -/T | 0.101658 | 0.201233 | intron-variant | UBR5 | GRCh38.p7 | 8:102391574 | TTATATACACACATA[-/T]TTTGCAAATATAGCA | 51366 |
rs148255677 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102275057 | ACATACCAGAAAGTA[A/C]GAAAGTTTATCAAAA | 51366 |
rs148278329 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102327020 | CCTCCTGCCTCAGCC[A/T]CCCAAGTAGCTGAGA | 51366 |
rs148278644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102410798 | TGGGAAGCGCATGAC[A/G]AACAGGGCATCATGC | 51366 |
rs148308009 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102315400 | GAGTTATTTAATACT[C/G]TGTTTAAGAAAATAA | 51366 |
rs148338262 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102385432 | GAATTACCTCTATCC[A/C]ACCCAAGTGACCTAT | 51366 |
rs148349682 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102260082 | ATTAACATAGTAGGA[C/T]TGATGTTACTCTTTA | 51366 |
rs148378767 | in-del | -/TTT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102269440 | AGAGCCAGAAATATC[-/TTT]TATTTAGGGTAGAAA | 51366 |
rs148383477 | snp | A/C | 5.04121e-05 | 0.00502031 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102286363 | TTTCAGACTTGCCTG[A/C]TGGTGTAGATGTACT | 51366 |
rs148391801 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102322950 | TGTTGTGGGGTGGGG[G/T]GAGGGGGAGGGATAG | 51366 |
rs148409869 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102272384 | TGTCCATTAGAATAG[G/T]TTAAACAAGATTAAA | 51366 |
rs148413041 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102364209 | TCTTTTGAGACTGGG[C/T]CTCACTCTGTCGCCC | 51366 |
rs148422616 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | UBR5 | GRCh38.p7 | 8:102406622 | ATTGCTTTTAGGTAA[C/T]AATCTCAATAATCAA | 51366 |
rs148434197 | snp | A/T | 0.000580407 | 0.0170255 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285684 | ACTGCTGGCGTTGCT[A/T]GCTTCCAAAGCAGCT | 51366 |
rs148435191 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102379174 | GTGGAGGAGTGAGTA[C/G]GGGTATATGCGAACA | 51366 |
rs148444384 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | UBR5 | GRCh38.p7 | 8:102307803 | GACATGTGCTCTTCA[C/T]TTGACTTCCAGGACA | 51366 |
rs148466406 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102357220 | CTTGAGTTTAATCAC[A/G]AGAAATGATAAACAA | 51366 |
rs148476857 | snp | C/G | 1.64972e-05 | 0.00287199 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311839 | TTCCTGTAGCAAGAT[C/G]AAAGATACAGTATCG | 51366 |
rs148495753 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102346055 | AACAAAGCAAGGCTC[C/T]GTCTCAAAAAAGAAA | 51366 |
rs148564360 | in-del | -/C | 0.0637235 | 0.166737 | intron-variant | UBR5 | GRCh38.p7 | 8:102370712 | CGTTAACCAACCTGT[-/C]CTTCATCCTACCTTC | 51366 |
rs148590506 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102330146 | TAACATAAAACAAAT[A/C/G]ATCAGAGCCACAAAG | 51366 |
rs148591556 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102292710 | ACAAGTCTGAAGATA[C/T]ACAGCTTGATTTGTA | 51366 |
rs148623815 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBR5 | GRCh38.p7 | 8:102401954 | AGGCATGGTGGCTCA[C/T]GCTTATAATCCAAGC | 51366 |
rs148644279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102332994 | CAGCCCAATAGCAAG[A/G]GCATGGTGCATGAGG | 51366 |
rs148649864 | in-del | -/AAAA | 0.304188 | 0.244057 | intron-variant | UBR5 | GRCh38.p7 | 8:102284272 | GAAATGTGATTTGAG[-/AAAA]AAAGAGCAGCACTGG | 51366 |
rs148654509 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102351781 | TATTAAAACAATTAT[A/G]CATCAGAAAACAACA | 51366 |
rs148677229 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102398261 | GGTGCTCAGAGAATC[A/G]GATGTCCATATGCAG | 51366 |
rs148706701 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102388943 | ATTGTTCGTTAGTAG[A/T]TACACTTCCATAATA | 51366 |
rs148715278 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102300401 | CACACAAACTTAAGC[A/C]CAGGGAACGAAAGCT | 51366 |
rs148791320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102375435 | CCAATATTAGCAGAC[C/T]AGGTTTTATAAAACA | 51366 |
rs148812818 | snp | C/T | 0.000938604 | 0.021643 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102305175 | CATCACATCTGTGGC[C/T]GATGAATGTCTGCAG | 51366 |
rs148815407 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102349148 | AAATGTCATGTTTAA[A/T]TAACTATTCATAGGC | 51366 |
rs148866740 | snp | C/T | 1.6534e-05 | 0.00287519 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285155 | GTGTTCGTAAGCTAG[C/T]TTCTTCTCGCGCAGT | 51366 |
rs148898444 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | UBR5 | GRCh38.p7 | 8:102296462 | CTGTGGTAACTGTTG[A/C]TGAATGAAAGACTGT | 51366 |
rs148932007 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102404128 | TTTACTGAATGTAAA[A/G]TATAACTCAATAAAG | 51366 |
rs148939978 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102317772 | TCAGACAGCAGCATT[C/T]GCGGTTCACGAAAAT | 51366 |
rs148949596 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | UBR5 | GRCh38.p7 | 8:102334615 | TTAATTAACAGTACC[A/G]AGTCAGGCGCCGTGG | 51366 |
rs148968358 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102262279 | CAAAGTATAAGAAGG[C/G]TTATATTTTGAAAAA | 51366 |
rs148972048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102353422 | CTTGCAAACTTAAAG[C/T]CCATGGGCCAAGTCT | 51366 |
rs148988755 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102276723 | GTCAACAAATCATAC[A/T]GAGCCACAGTATATA | 51366 |
rs149076654 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | UBR5 | GRCh38.p7 | 8:102387474 | GCACTTTGGGAGGCC[A/G]AAGCAGATGGATCAC | 51366 |
rs149115655 | snp | A/G | 0.00755907 | 0.0610114 | utr-variant-3-prime, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102254199 | TTAAGGTACCACCAG[A/G]GGGGTATGACAGCAT | 51366 |
rs149139339 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | UBR5 | GRCh38.p7 | 8:102366038 | TTTCTTGCAGAATTT[C/T]TAAAGCAAAAAAAAA | 51366 |
rs149161467 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | UBR5 | GRCh38.p7 | 8:102381734 | TCCTTCAAATTATAA[A/G]AACAAATATAATTTT | 51366 |
rs149169387 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102289708 | CTGAGCTGAGAATTC[C/T]TAGAAACCAACAATA | 51366 |
rs149173780 | in-del | -/AATCTGTGTT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102289786 | TTTTAAGTCATTTCA[-/AATCTGTGTT]GATGCACATTATTTG | 51366 |
rs149179879 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102310205 | CACTGCTAAAATCCA[A/G]TTACCAAGCTTTACA | 51366 |
rs149204297 | snp | A/G | 0.0573587 | 0.15934 | intron-variant | UBR5 | GRCh38.p7 | 8:102323872 | TGGGAGGCTGAGGCA[A/G]AGAATTGCTTAAACC | 51366 |
rs149248956 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102405968 | AAATTTTCCTTTGGA[A/T]ACTATTTCCTAAATA | 51366 |
rs149256330 | snp | C/T | 0.000223554 | 0.0105701 | intron-variant | UBR5 | GRCh38.p7 | 8:102285108 | TGGGGACGTTCTGTA[C/T]ATATGAAGAATTTCA | 51366 |
rs149266477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102337024 | AAGTGCTGAGATTAT[A/G]AGCATGAGCCACAGC | 51366 |
rs149290918 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102264221 | CGTAGGTCTGTCAGA[A/C]CCCCCAGCCCCACTT | 51366 |
rs149298024 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102373195 | TTTTCAGCTCCGTTC[A/G]AAACAGGAAAAGGAA | 51366 |
rs149302650 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102401296 | TGTCAATTGAAGAAG[A/C]TTTTACATTCCCAGA | 51366 |
rs149308204 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102279311 | CAAAATTCCTACTAC[C/T]TCTTTTATAAAATTT | 51366 |
rs149374385 | in-del | -/AAAG | 0.0566069 | 0.158427 | intron-variant | UBR5 | GRCh38.p7 | 8:102257355 | TGTAGGCAGTGCGAT[-/AAAG]AAAGATAAAAAGCCA | 51366 |
rs149384141 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | UBR5 | GRCh38.p7 | 8:102397574 | GGCATGGTGGCGGGC[A/G]CCTGTAATCCCAGCT | 51366 |
rs149412815 | snp | A/G | 0.000462199 | 0.0151949 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102275750 | CATGAATACCCTGCC[A/G]AACAGTTCTAAAGAA | 51366 |
rs149424540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102257131 | AAGAGGTAGACTTTC[C/T]ACTAAGATCAAAGCT | 51366 |
rs149428571 | snp | A/T | 0.00694944 | 0.0585357 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102345457 | GTAACCAAAATAGCT[A/T]ATGTCTTCAGAAAAC | 51366 |
rs149438784 | snp | A/C/T | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102392156 | TTACCAGTGTGATTG[A/C/T]TGAGAGTTGGCCTGT | 51366 |
rs149481132 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | UBR5 | GRCh38.p7 | 8:102384617 | GGTGGAAGAGAGGAG[C/T]TTGAGGCGAAGAAGA | 51366 |
rs149490481 | in-del | -/AGAC | 0.0107246 | 0.0724382 | intron-variant | UBR5 | GRCh38.p7 | 8:102325856 | GTCAGACTTAATAAA[-/AGAC]AGCTGTATTCTCACG | 51366 |
rs149501088 | snp | G/T | 0.00145627 | 0.0269447 | intron-variant | UBR5 | GRCh38.p7 | 8:102311548 | ATCAAAAAATGTATC[G/T]GATTTTTACAGGCAT | 51366 |
rs149554816 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102351189 | AATTGCATGTCTGGT[A/G]TATATTCGAAAGAAT | 51366 |
rs149555073 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102315032 | AGAATAAAAGGTACA[C/T]AATGCATGCTTTCAA | 51366 |
rs149657371 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102272077 | AACAGTGAGCTTAGT[C/G]ACACAGTGGATTTGC | 51366 |
rs149703917 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102399164 | ATGGCCAGTTAGTGT[C/T]GGATACAAAGAACAA | 51366 |
rs149732027 | snp | C/T | 3.30322e-05 | 0.00406387 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102281490 | CGTGCAGACATCATT[C/T]CTTGACGGGCGCTAA | 51366 |
rs149733852 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102348898 | ACTGGAAAGCCCAAT[A/C]TCTGGCTAAATAAAA | 51366 |
rs149744836 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102259896 | AGCTGGGCATGCTGG[C/T]GCGCGCCTATAGTCC | 51366 |
rs149786726 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102386959 | CCAGCTGGGTGACAG[A/G]GCAAGACTCCGTCTC | 51366 |
rs149793011 | snp | A/G | 0.000198255 | 0.00995431 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102261188 | CATTCTGTGTTCTGC[A/G]TATTTCCGCACATAC | 51366 |
rs149826380 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102329727 | TCTCTGATGACACTA[C/T]GTACAGAACCACCAC | 51366 |
rs149864293 | in-del | -/AG | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102361448 | GCCCAACCCATAAAA[-/AG]TTGACAGATTAAAAG | 51366 |
rs149869919 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | UBR5 | GRCh38.p7 | 8:102316583 | AAGATCTCTGTACTA[C/T]GCTCCAAACAGAAGT | 51366 |
rs149874223 | snp | A/G | 0.000809242 | 0.0200989 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102323388 | AAATCTACAGCTGTC[A/G]TTCATATTCCAAACT | 51366 |
rs149880106 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102369285 | TATTATTCTTTGATA[C/T]TATACCAAAACTCAG | 51366 |
rs149990528 | snp | A/G | 6.60371e-05 | 0.0057458 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102259028 | GATCAGCATTTGCAC[A/G]TTGACTTCACCGCAG | 51366 |
rs150008780 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102339073 | CAAGATGCCTATAAT[C/T]TTCAATTATGCTTTT | 51366 |
rs150040041 | snp | C/T | 0.159622 | 0.233092 | intron-variant | UBR5 | GRCh38.p7 | 8:102375115 | CCTGCAATCCCAGCA[C/T]TTTGGGAGACCAAGG | 51366 |
rs150081463 | snp | A/T | 0.0368353 | 0.130617 | intron-variant | UBR5 | GRCh38.p7 | 8:102378439 | ACTTGAGGTCAGAAG[A/T]TCCAGACCAGCCGGG | 51366 |
rs150093037 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102336658 | AAATTAGTTAATAAT[A/T]TATGTTTGAATTTAC | 51366 |
rs150102939 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102388426 | AATACACACAATAGT[A/G]GTATTTCAGTGCAGA | 51366 |
rs150111343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102262252 | TCTTTGGCTCTGACA[A/G]TATTTGCTTTTCAAA | 51366 |
rs150120930 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102313663 | ATCTGCATCAGATGC[A/G]GGGGTGCAACTAAAG | 51366 |
rs150144413 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBR5 | GRCh38.p7 | 8:102331844 | GCACTACCATGCATG[A/G]TCTTCCCTCCATCTC | 51366 |
rs150186712 | snp | C/T | 4.94409e-05 | 0.00497172 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102360154 | CCTACCAGGCCTTGA[C/T]GTCCTCCCTGCCCCC | 51366 |
rs150223536 | in-del | -/A | 0.00716266 | 0.059414 | intron-variant | UBR5 | GRCh38.p7 | 8:102403969 | GCCAGGACCTAGCCT[-/A]GGGGGAAGTGACTGA | 51366 |
rs150262268 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102391927 | CCACCAAAATCGAGA[C/G]AGCAATGTAAGTGAC | 51366 |
rs150300466 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102291405 | TGTCTCTTGGGCTAG[A/T]AGGGCTTCAAGGAAC | 51366 |
rs150308260 | snp | A/G | 0.000387639 | 0.0139165 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102271136 | ATACAAAATTTACCT[A/G]TCCCGGTCCCTCCGA | 51366 |
rs150313456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102343001 | TTTCATTAGAAATGC[A/G]TACTATAAATTCAAT | 51366 |
rs150332194 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBR5 | GRCh38.p7 | 8:102359214 | GCCTTCAAACACGTG[A/G]TGACTGAAGTAGCAT | 51366 |
rs150344941 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | UBR5 | GRCh38.p7 | 8:102376400 | ATGCATGAAATATCT[C/G]TGGAAGGAATAATAC | 51366 |
rs150347502 | in-del | -/A | 0.0528381 | 0.153711 | intron-variant | UBR5 | GRCh38.p7 | 8:102349223 | CAAAAAAAGGAAATT[-/A]AAAAAACAATCCAGG | 51366 |
rs150356110 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102284530 | AGTAATGCAAGCAAG[C/T]CATTTCTTTCTCCCT | 51366 |
rs150466657 | snp | C/T | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102288214 | TCTTCCCCGTGTTCT[C/T]CCTGTTCATCATGAT | 51366 |
rs150471796 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UBR5 | GRCh38.p7 | 8:102351120 | GAACAACCACTTTCG[A/G]AAAACAATATGGAGA | 51366 |
rs150492938 | snp | A/C/G | 0.00517822 | 0.0506191 | intron-variant | UBR5 | GRCh38.p7 | 8:102273714 | AACAACCATTAAAGT[A/C/G]CAGTACATTAAGCAG | 51366 |
rs150495142 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102396958 | TGATCTGCCCATCTC[A/G]GCCTCCCTAAGTGCT | 51366 |
rs150570300 | in-del | -/AAAAAC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102370114 | TTCTTCTTACTAAAA[-/AAAAAC]CAGCCACAAATGCCA | 51366 |
rs150628620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102310919 | TATCAAAAAAAAGTA[C/T]TTTCTCCCAACTTAT | 51366 |
rs150653683 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | UBR5 | GRCh38.p7 | 8:102362422 | AAGTTATCAAAAAAA[A/C]CACTGCCTGATCTGA | 51366 |
rs150662974 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102379596 | AACCATTCTACAGAT[A/G]TGGTTGGTCCTGTTA | 51366 |
rs150714210 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102411430 | CATTTCAGGAGGAGA[G/T]TAAAGGGAATCCAAT | 51366 |
rs150786432 | snp | C/T | 4.94621e-05 | 0.00497279 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295481 | GTATTGACAATGCTC[C/T]ACCGTCTGCCTTGCG | 51366 |
rs150810093 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBR5 | GRCh38.p7 | 8:102368699 | TTCAAATGATCCCGT[C/T]TGCCTTGGGCTGCCA | 51366 |
rs150810243 | snp | C/T | 0.00565242 | 0.0528608 | intron-variant | UBR5 | GRCh38.p7 | 8:102275638 | AAAAAAAAAAAAATG[C/T]ATGACAGATTATTCC | 51366 |
rs150820680 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102338453 | CATGCATGATCTGTA[C/T]CTTTTTGGTCTGTGT | 51366 |
rs150840501 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102264084 | ACCAGGTACAACTAA[C/T]AATAGTGGATACAAT | 51366 |
rs150844122 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102389100 | ATCACTATTCTTAAC[A/G]ATCACAGTGGTTTAA | 51366 |
rs150852670 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBR5 | GRCh38.p7 | 8:102400379 | ACTCTTCTCCAAGCT[C/T]TCTCCCTGAGCCAGA | 51366 |
rs150863977 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102315701 | TACTCCTGGCTGCTC[C/T]ACAAATGCTGTGATG | 51366 |
rs150874442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102333596 | CAGCAACACCAACTC[C/T]ATTAACTGGCCACAC | 51366 |
rs150893060 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102260136 | GCATTGGCTGGTGTC[A/T]GAGAACTTGGTTTTT | 51366 |
rs150950971 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102313144 | ACCCATGAACTACAG[G/T]TCTATTTTGAGAATC | 51366 |
rs150957689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102364895 | GCCTGTGATAACATT[C/T]GTTTAAATTTGCTAA | 51366 |
rs150979416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102259354 | AAGCTATGGGTTCAA[C/T]AGTGAAGTAGTATTA | 51366 |
rs150983551 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102382167 | TGCCACACCTGCCAC[A/G]GGTCCAATTCAATTA | 51366 |
rs151001883 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBR5 | GRCh38.p7 | 8:102393944 | TAAAAAATAACAATA[A/G]AAAGTTTCTAGAGGA | 51366 |
rs151002496 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102307978 | TCTTGTTCAATATAA[C/T]TCCTCTAAATAAACA | 51366 |
rs151118446 | snp | A/C | 0.000253947 | 0.0112654 | intron-variant | UBR5 | GRCh38.p7 | 8:102277221 | CATTTAAAAGTTACA[A/C]ATGAAGGGAAAAAAA | 51366 |
rs151119071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102370600 | AGATCTTCTCTTCAA[A/G]CTATTTGGAAACATA | 51366 |
rs151131085 | snp | A/G | | | upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102412747 | CCGGAGCGGCGGGGG[A/G]GGGGCAAACGGGAGG | 51366 |
rs151150075 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | UBR5 | GRCh38.p7 | 8:102391138 | GGTGCCACTGCACTC[C/T]ATCCTGGGCAGCAGA | 51366 |
rs151161778 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | UBR5 | GRCh38.p7 | 8:102358221 | CAGTATATAAACTGA[C/T]AAGCAAAACCTGGGA | 51366 |
rs151161908 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102265608 | TTGATGAGTTTGTTG[A/C]CTTTTGGCTTTCATA | 51366 |
rs151171777 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBR5 | GRCh38.p7 | 8:102402207 | AGTGACAGAGTGAGA[C/T]CTTGTCTCAAAAAAA | 51366 |
rs151177011 | snp | C/T | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102268981 | TGTACACATTACCGT[C/T]CATGTGCAATAATGA | 51366 |
rs151215250 | snp | G/T | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102352091 | GATGGGCGGATCACT[G/T]GAGGTCAGGAGTTCG | 51366 |
rs151252698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, nc-transcript-variant | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102252063 | TGTTTGGGGGCAGCT[A/G]CTAAATAGTGAAATC | 51366 |
rs151274652 | snp | C/T | 0 | 0 | intron-variant | UBR5 | GRCh38.p7 | 8:102331692 | TCAATGCTCAATGTA[C/T]GTAATCAGTCCATCT | 51366 |
rs151318993 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102273541 | AAAATTATATGCACA[C/T]GCTCTTTGACCCAGC | 51366 |
rs151328905 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102324644 | TGTAAGAAACAAAAG[A/G]AGATGGTGGTACATT | 51366 |
rs151330682 | snp | C/G | 0.0475351 | 0.146656 | intron-variant | UBR5 | GRCh38.p7 | 8:102407517 | TGCCTGTAATCCCAG[C/G]ATTTTGGTAGGCTGA | 51366 |
rs180683815 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102328163 | TTTGCTCTACCAATT[G/T]TTAAAAGAATTTAGT | 51366 |
rs180689915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102343058 | CGTTTGTCTACTGGT[A/G]GGTTTAAAAAGCACA | 51366 |
rs180713717 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBR5 | GRCh38.p7 | 8:102391112 | AGGTTGATGCTGCAG[C/T]GTACAGTGATGGTGC | 51366 |
rs180720729 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102287873 | GGGTGATTTATTTTC[C/T]TTTTCTCTAATTTCC | 51366 |
rs180724177 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102268390 | TTTTTTTTTAGTAGA[C/G]ATACGGTTTCACCAT | 51366 |
rs180731292 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102377639 | GGAACCCAGGAGGCA[A/G]AGGTCGCAGCGAGCA | 51366 |
rs180742524 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102359952 | GCCCAGAGTTCAGGA[G/T]AATTTTCTCACTCCA | 51366 |
rs180755048 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102399027 | TATATGATGAAAAAA[A/C]GCTATTCCCTACCAC | 51366 |
rs180761849 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102408399 | TTACCTTGTGTTATG[A/T]CACCTGAAAGGGAAA | 51366 |
rs180767604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102370262 | GCCTCCGCCTCCCGG[A/G]TTCTAGCGATTCTCC | 51366 |
rs180780440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102353503 | GAAAAGTCTGAGAAA[C/T]GGTCACAGTCAAGAG | 51366 |
rs180929243 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102265534 | TGAAACTCGGATAAG[A/C]TTCTTTCACTTTATT | 51366 |
rs180932369 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102283140 | AACAAAATATAGTAC[A/G]CTCATACAATGAAAT | 51366 |
rs180945569 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102254086 | CTGGGGTTAGACCCA[A/G]AAGTTGGTGACTAGC | 51366 |
rs180962276 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102290066 | AAAGGCAAAGTGGCA[A/C/G]AAGTTTCACTTCCCT | 51366 |
rs180969541 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102312837 | CTTGAAAATGGCAAC[A/G]TTCTATATTGGCGGT | 51366 |
rs180991295 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102322859 | AAAACCAAACAACGC[A/G]TATTCTCACTCATAG | 51366 |
rs180996767 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102273882 | GTTTTAAAAGGGAGG[C/G]AAGGAAATAAACTTG | 51366 |
rs180997412 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102338001 | TCCAGAAATGCAAAA[C/T]GTAATAAGCAGTCAT | 51366 |
rs180999461 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102396138 | AAAGCTCTATTTTCT[G/T]CCCACTACTCCTAAA | 51366 |
rs181010482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102387105 | TGTTAAATAAAACAA[C/T]GTTTGGAAAACACAG | 51366 |
rs181026866 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102355847 | TCAGAAAACTAAGGA[G/T]TCTGTCTGCATTTTA | 51366 |
rs181032803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102373133 | ACAGGTGTGAGCCAC[C/T]GCACCCAGCCCAGTC | 51366 |
rs181061182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102403567 | AATTAAAATAATAAA[C/T]AAACAAGAAAAAAAT | 51366 |
rs181103680 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102254992 | ATTTACTGCTACATT[G/T]TGATACAGAATCATT | 51366 |
rs181114478 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102274050 | AATGAAACAAAAGGC[C/T]CTAATTATATAGAGC | 51366 |
rs181180615 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102290459 | AAAAGTGGGAAAGGC[C/T]AAGAGAAAATCTGTA | 51366 |
rs181227827 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | UBR5 | GRCh38.p7 | 8:102323071 | TTGTGCACATGTACC[C/T]TACAACTTAAAGTAT | 51366 |
rs181236859 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102345899 | AACCCCGTCTCTACT[A/G]AAATACAAAAAATTA | 51366 |
rs181253742 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102338458 | ATGATCTGTATCTTT[C/T]TGGTCTGTGTCCAAT | 51366 |
rs181254751 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102380514 | CACATATTACAAGTC[A/G]AAGATTAAGGGGAAA | 51366 |
rs181260956 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBR5 | GRCh38.p7 | 8:102304855 | TCAGTAAAGTTCATT[C/T]AGCATTACATATCCA | 51366 |
rs181270295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102313077 | GGTCCCACTTCTGCT[A/G]CTTGATGCTTTTTAT | 51366 |
rs181280232 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102387937 | CTGTCTAGTCTCACA[A/T]CCTTGTCTTATGAGT | 51366 |
rs181285223 | snp | C/T | 0.0182019 | 0.0936463 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102413939 | CCAACTTGGTGAAAC[C/T]CCATCTCTACTAAAA | 51366 |
rs181287284 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102373975 | GTCACAGAAACCTGG[A/G]TTTGATTCCATCTCT | 51366 |
rs181301362 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102356280 | CATGGTGAAACCCTG[A/T]CTCTACTAAAAATAC | 51366 |
rs181318106 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102404435 | CCAAGTTCAATTGAC[G/T]AATACCTCACCTGTC | 51366 |
rs181336268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102365321 | AATTCAAAAATTAGC[C/T]GGGTGTGGTGGTGCA | 51366 |
rs181363662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102332734 | CCCCTATAGCACTTT[A/G]CTCATACTTTCAGCC | 51366 |
rs181368597 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102274519 | GGTGGATTACTTGAG[G/T]TCAGGAGTTTGAGAC | 51366 |
rs181372139 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102291338 | GAAACGACTGTACTG[C/T]ATAAAGCTTGGAGAG | 51366 |
rs181375065 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102314554 | AAAACAACAGAAATA[C/G]TCAACACTGTAAATA | 51366 |
rs181386044 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102394445 | TATCAAGAAATATCA[A/G]AAGTAATCAACCATA | 51366 |
rs181405715 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102255896 | GAGTTTAAGGTTCAC[A/T]AACTAAAGCTGTTGA | 51366 |
rs181407182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102402638 | TCACGGAAAACACCC[A/G]AATGAATTTCCACCA | 51366 |
rs181410859 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102365827 | CATTGCTATACTTTA[A/G]ATCCCCTCTAATTTC | 51366 |
rs181416946 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102386845 | GCCTGGTGTGGTGGC[A/G]GGCACCTGTAGTCCC | 51366 |
rs181432672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102333099 | CCAATTACACCCCTA[C/T]AGGCCCTGAAAACCC | 51366 |
rs181438921 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102346595 | CCGTCTCTACTAAAA[A/C]ATACAAAAATTAGCT | 51366 |
rs181476922 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102337582 | CACATTGATTAATGT[G/T]TATATATAAAGTCAG | 51366 |
rs181496211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102264852 | TAGCTGGGACTACAG[A/G]CATTGCAGCACAATG | 51366 |
rs181510014 | snp | A/G | 0.0860495 | 0.188743 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102304000 | TGCTTTCTGTACTTG[A/G]TTTTTTCCTCCAATT | 51366 |
rs181527893 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102372470 | TTTATTAATGCTTAT[A/G]AAGATGATAAATGCC | 51366 |
rs181569841 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102395401 | ATCTATTTATATATA[C/T]ACACACACACACACG | 51366 |
rs181583620 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBR5 | GRCh38.p7 | 8:102278101 | GGTACTTAAGTCTCA[C/T]ATATTTTTAATATTT | 51366 |
rs181585120 | snp | C/G | 0.0126979 | 0.078662 | intron-variant, downstream-variant-500B, nc-transcript-variant | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102251864 | AAAGACTTACTGAAT[C/G]AGAAAGGAGGCAAGA | 51366 |
rs181586040 | snp | A/C/T | 4.95621e-05 | 0.00497785 | intron-variant | UBR5 | GRCh38.p7 | 8:102295576 | GGAGGCTGAAAAGCT[A/C/T]CTCAGCTGTGCTGCG | 51366 |
rs181597869 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102316942 | TATATAAATATGAGG[A/G]GGGAGGAGCCAAGAT | 51366 |
rs181599192 | snp | A/G | 6.61671e-05 | 0.00575145 | intron-variant | UBR5 | GRCh38.p7 | 8:102270191 | TAAAGTCTCTGTAAG[A/G]GAAGGAAAACTATTA | 51366 |
rs181619025 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102355754 | ATGCTTAAAGAACGC[G/T]TACACAGTCTGTTCT | 51366 |
rs181624260 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBR5 | GRCh38.p7 | 8:102369427 | GAAAACACTGATTTA[C/T]TGACTGACACAGATA | 51366 |
rs181630749 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102283009 | AACTAGGTATATATT[C/G]AAGAGAACTGAAAAC | 51366 |
rs181645134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102335312 | TGGGGTTATAGGATA[C/T]ACAGCAGACATGTAG | 51366 |
rs181651548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102351232 | CTTAAAGAGATACTT[A/G]CAAACCCATGTTCAA | 51366 |
rs181657718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102384878 | TAAAGGCCTGACCTT[C/T]AAACTAAATCAAGAG | 51366 |
rs181673703 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102414152 | TGTTTTTTTTTCCCT[A/G]AGGAACCAATTCATG | 51366 |
rs181725741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102409007 | CCCCTCAAGCTCGAC[A/G]AACCACATTCTTTAT | 51366 |
rs181809646 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102260447 | AGTGTGTTCTTTGCA[A/G]TAACTCATTCCCCTG | 51366 |
rs181842396 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102267917 | TTTTTTTTGAGACAG[A/G]GGCTCGCTCTGTCAC | 51366 |
rs181854159 | snp | A/G/T | 0.000248843 | 0.0111518 | intron-variant | UBR5 | GRCh38.p7 | 8:102288318 | AGTTAACTAAAATGC[A/G/T]AAGACCACTAACTAT | 51366 |
rs181857057 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102287140 | CACTGGAATATCCAG[C/G]CTGGTGACAGAATGA | 51366 |
rs181859609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102360772 | GTCAATTCAGAAGAC[A/G]ATAAATAAACTTCCT | 51366 |
rs181866287 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102328464 | ACAATTTAGTGACTT[C/T]AAAGCCAAATCGATA | 51366 |
rs181878116 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102398260 | TGGTGCTCAGAGAAT[C/T]GGATGTCCATATGCA | 51366 |
rs181886838 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102391609 | CTTAGTAAGTTAGGC[A/T]GGAATATCATCACCC | 51366 |
rs181888292 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102385301 | CTAACTCAATACCTG[C/G]ACATAACTGAAGTTC | 51366 |
rs181896280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102369710 | GGGCTTGTTTTAAAA[C/T]GATCTTATGCTCAAA | 51366 |
rs181909839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102308621 | TGTACAGTATAATAT[C/T]CGATAATGATAAAAC | 51366 |
rs181915631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102326193 | CATAGAGCAGTATCT[C/T]TCAAACGGGTTAGTC | 51366 |
rs181917855 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102342915 | TATATTTCAACTACA[C/T]GGTTTTAGAGTGGAA | 51366 |
rs182049579 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102317202 | CAAGGAAAGGGGTGA[C/T]AGACAGCACCTGGAA | 51366 |
rs182069376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102352299 | GGGTGACAGAGTGAG[A/G]CTCTGTCTCCAACAA | 51366 |
rs182081188 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | UBR5 | GRCh38.p7 | 8:102343285 | AGACAGGCTTTTTTT[A/T]AAAAATAATCTTTAT | 51366 |
rs182094140 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102344748 | AGCCTGGCTAACATG[A/G]TGAAACCCCGTCTCT | 51366 |
rs182100935 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | UBR5 | GRCh38.p7 | 8:102261676 | CACTACACTCCAGCC[G/T]GGCGACAGAGCAAGA | 51366 |
rs182105670 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102362842 | TCTAATATTGAATTG[C/T]ATTCAGTAACTGAAA | 51366 |
rs182107632 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102280878 | GGCATGGTAGCACAC[A/G]CCTGTAAGTCCTATA | 51366 |
rs182111160 | snp | G/T | 0.000378552 | 0.0137526 | intron-variant | UBR5 | GRCh38.p7 | 8:102296992 | AAAATATCCTAAAAT[G/T]AAGAGTGTACTTTTA | 51366 |
rs182114368 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102377823 | TTTATGATTCAAAAG[C/T]GCCTTGTTTTAGGAG | 51366 |
rs182114556 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102309384 | TTAAGCATATTATTA[C/T]TACAAACAAATCAAA | 51366 |
rs182115995 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102397622 | AGGAGAATTGCTTGA[A/C]CCCAGGAGGTGGAGG | 51366 |
rs182122076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102411138 | GGCAAGGAACGGTGG[C/T]GGAAGAAAAGGAGAA | 51366 |
rs182124128 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102392857 | ACACTCACAAGCACA[A/T]ACTGAAGGAAGGCAA | 51366 |
rs182137204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102378738 | CGCTGACTCAACAGA[C/T]TCAACAAGCGGTTCC | 51366 |
rs182154429 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102317325 | TCCTACGCTCAGAGT[A/C]TCGCTGATTGCTAGC | 51366 |
rs182281688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102284809 | TGGGAGGCCAGGGTG[A/G]GCAGATCACAAGGTC | 51366 |
rs182300659 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102325214 | AAGAAACTAATATAA[A/C]TAATGAAGGCCGATC | 51366 |
rs182301540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102260909 | CCTTTCCACACTTTT[A/G]TTTGCCAAAGCTACT | 51366 |
rs182302571 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102366574 | GTCTCAAATTAAATA[C/T]GTGAGCAGTGTGAAT | 51366 |
rs182314140 | snp | A/T | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102266961 | CCTGTACCTTTTCTG[A/T]GGAGTCTACTAATCC | 51366 |
rs182335513 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102357147 | ACATGCCACCTGATA[A/T]GATGCACTGAAAAGG | 51366 |
rs182337887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102381385 | ACGAACAAACAAAAC[C/T]ATCAGATCTCATGAG | 51366 |
rs182346956 | snp | A/C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102340408 | CACCCTATCTCCCTG[A/C/T]ATTCTCCACCTACCT | 51366 |
rs182389827 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102296395 | AAACACCACAGATGT[C/T]AGTGCTAGGTATTTC | 51366 |
rs182395898 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102359756 | TGTACCAAGAATAAG[C/T]TGTAAGAGAGGACCA | 51366 |
rs182454096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102273495 | CAAAATTATGCAACT[A/G]CTTATGCAGAAGTAT | 51366 |
rs182460357 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102335886 | CATCTCCTCTGGGTA[C/T]GTACATAATAGGGAT | 51366 |
rs182467613 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102309954 | ACCCTAGTACTCTCA[C/G]CACGTCATAAGGAAT | 51366 |
rs182571818 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102406619 | AGTATTGCTTTTAGG[A/T]AACAATCTCAATAAT | 51366 |
rs182583578 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | UBR5 | GRCh38.p7 | 8:102390011 | TGATCTGCCCGCCTC[A/G]GCCTCCCAAAGTGTT | 51366 |
rs182619078 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102252450 | AAAATAAATTCACAA[C/T]TAGGGTTTCAAATGT | 51366 |
rs182634395 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102276127 | GTCTATCTCCATTTA[A/G]GTGACTCCCAGATCC | 51366 |
rs182639634 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102257502 | ACAAAAACTGCCTTA[C/T]TTGTGACCTTCTATA | 51366 |
rs182658138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102292969 | TATTAACAGAGATGT[C/T]TTCCAGAAAAGGAGG | 51366 |
rs182663774 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102329861 | CTTATTCACCACTGT[A/T]ACTTAAGAACTTAGC | 51366 |
rs182698297 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102288756 | GAGCATATACAGAAC[A/C]CTCAAGTTAGAAGTA | 51366 |
rs182706022 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102315136 | TCTAGAAATAACGAA[A/G]TTTACACTTAATTTA | 51366 |
rs182714463 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102291964 | GTAATCTGTCTACAA[A/T]ACTTAGGAAAGTTCC | 51366 |
rs182730092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102266715 | TCAAGCTGTGCTCAA[A/G]TGGATGCCAACCAAT | 51366 |
rs182761940 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102388838 | AGAAACACATTTATA[C/T]TGACTTGCCTTGTGA | 51366 |
rs182910206 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UBR5 | GRCh38.p7 | 8:102315642 | AACTGGTATTATTTT[C/T]ACCAGGATCTTAACA | 51366 |
rs182916885 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | UBR5 | GRCh38.p7 | 8:102334268 | CTAGACTAGATAGAA[A/T]TAGATCCAGAACAGT | 51366 |
rs182923342 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102348891 | TCACTTGACTGGAAA[G/T]CCCAATCTCTGGCTA | 51366 |
rs182940418 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102293167 | AACTTGAAAGGCATA[A/C]GAAGTTGGAGGCCCC | 51366 |
rs182954866 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102382861 | ACACACACACACACA[C/G]AGAGACACACACACT | 51366 |
rs182959617 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102368178 | CAGTAAGGCCATAAT[C/G]TTGCAATAAATAAAC | 51366 |
rs182962270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102405051 | CATGTTAGAACCCAA[C/T]CAGCTTTATTAAGTA | 51366 |
rs182964035 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102346758 | AGACTCCCTCTCAAA[A/G]GAAAAAAAAAAAGTT | 51366 |
rs182987171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102275217 | TTAAATCAATGCATG[C/T]ATAATGATACTTAAA | 51366 |
rs182996356 | snp | C/T | 0.000203839 | 0.0100935 | intron-variant | UBR5 | GRCh38.p7 | 8:102314739 | ATACAACAAATAAAA[C/T]TTACTGTATGGCATT | 51366 |
rs182997610 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102284129 | TACTGCTATTGCTCT[A/G]ATGTTCAATATTTGA | 51366 |
rs183003547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102375187 | GTAACATGGCAAAAC[C/T]CCATCTCCACTAAAA | 51366 |
rs183029095 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102406204 | TGCTGTTAATCTTAC[C/T]TAAGCAAATTCATTT | 51366 |
rs183042014 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102381898 | CTAATCATGGACTGT[A/G]AAGATTTTCTTAGAA | 51366 |
rs183049412 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102347725 | CTCACTGCAACCTCC[A/G]CCTCTGCCTCCTGCG | 51366 |
rs183083205 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102412431 | GGCGGGCAGGAGGGC[A/G]AATCCACACGCCACC | 51366 |
rs183122298 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | UBR5 | GRCh38.p7 | 8:102297837 | CCAATACAAACACAC[A/T]ATACATCAGCCATCT | 51366 |
rs183125099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102317583 | ACAGCTTTGAAGAGA[A/G]CAGTAGTTCTCCCAG | 51366 |
rs183137826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102336529 | CTTTTGTCTATTTTG[A/G]GTCGATCTTTATGTA | 51366 |
rs183171024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102385786 | TACTGCTATTCTACC[C/T]TTTACATTTCTATTT | 51366 |
rs183178238 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102370382 | ATGTTGGCCAGGCTG[G/T]TCTCGAACTCCCGAA | 51366 |
rs183189326 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102353963 | TTGAGCCCAGGAGGC[A/G]GAGGCTGCAATAAGC | 51366 |
rs183202797 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102288622 | GAATTGCTTGAACCC[A/G]GGAGGTGGGGGTTGT | 51366 |
rs183207712 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102399529 | TGATCAGCCAGCTTC[C/G]GCCTCCCAAAGTGCT | 51366 |
rs183209039 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102309635 | TGTAAACAACTACTT[A/C]TCACTGTGTTACAAA | 51366 |
rs183212625 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | UBR5 | GRCh38.p7 | 8:102328731 | AGCTGGTATTACAGG[C/T]GCCTGCCACCACACC | 51366 |
rs183228646 | snp | A/G | 1.67556e-05 | 0.0028944 | intron-variant | UBR5 | GRCh38.p7 | 8:102272815 | AGTAGTAAATTCAAT[A/G]TTGGAAAGTAGCTTG | 51366 |
rs183232296 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B, nc-transcript-variant | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102251966 | AACTACTGCCTCAAG[A/G]GATTATCTCAACTTG | 51366 |
rs183242558 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102361968 | AACCAAAGGCTCAAT[G/T]GTTTAAAAAAACAAA | 51366 |
rs183257908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102265769 | TTTCAGTTTATTCTG[C/T]TGAGTTCACTGACTC | 51366 |
rs183272843 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102344302 | GTTAACTTTTAAGGA[G/T]TTCAAACTTTTTTTT | 51366 |
rs183290662 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102338946 | TTTCTTCTTCCTATA[A/C]AATCTCTCACCCTAA | 51366 |
rs183296419 | snp | C/T | 0.0663309 | 0.169604 | intron-variant | UBR5 | GRCh38.p7 | 8:102396649 | ACACACATATATATA[C/T]ACACACACACACACA | 51366 |
rs183313538 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102366966 | AGATAAATTCTGCTA[C/G]AAAAAGAAATACTGT | 51366 |
rs183314924 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102374402 | CTTGTTTCTTATACA[C/T]GAGTTTTTATTTCAG | 51366 |
rs183394267 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102385838 | ACCCTTAAGGATAAG[G/T]AAGGCCTGTAATTTT | 51366 |
rs183447473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102401090 | CTAACTGGGAAAAGC[C/T]ACCACAATCCATGAT | 51366 |
rs183481663 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102284462 | CCTACGATATGAATG[C/G]ATTTTTAAAAACAGC | 51366 |
rs183499291 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102282372 | AAAAGACAAACCAAT[G/T]TAAAAAATGGGCAAG | 51366 |
rs183502948 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102302117 | TTCCTTGTCATTTTT[A/T]AAATTGTCCTTAACC | 51366 |
rs183533788 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102263924 | TAGAGTCAGAGTCTC[A/G]TACGTTGTCCAGGCT | 51366 |
rs183535619 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBR5 | GRCh38.p7 | 8:102356562 | CAGGAGATCGAGACC[A/G]TCCTGGCCAACATGG | 51366 |
rs183561123 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102324016 | TTAAGGAAAAGGAAT[A/G]ATTTCAACATGTTTG | 51366 |
rs183568318 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBR5 | GRCh38.p7 | 8:102262959 | GGCATGGTTGTATGC[A/G]CCTGCAGTCCCAGCT | 51366 |
rs183572611 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102336949 | TAAGTTTAAAAATAC[C/T]AATTCTTCCCATCCA | 51366 |
rs183587790 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102388218 | CAATAAACTTTACAT[G/T]CAAACAGATGTGTCT | 51366 |
rs183620786 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UBR5 | GRCh38.p7 | 8:102393352 | TCTGAATGTAAAAAC[A/G]GAAACAACAGGCGGT | 51366 |
rs183623698 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102330723 | ACTTATTAAGTATGT[A/G]ACTTCAGGTAAACTA | 51366 |
rs183639239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102363387 | TTTGCCCATTTACAA[A/G]GCACACTTCTGTGTT | 51366 |
rs183717624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102380269 | CATGGTGGTACACGC[C/T]TGTAGTCCCAGCTAC | 51366 |
rs183725672 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102364891 | GCAGGCCTGTGATAA[C/G]ATTCGTTTAAATTTG | 51366 |
rs183753666 | snp | A/T | 0.0162398 | 0.0886349 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102413474 | AAAATTATTATTTTT[A/T]TTTTTTTTTTCCCCG | 51366 |
rs183759452 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102394357 | GAGCCACCGCATCCG[G/T]CCAGAATTTATTCTT | 51366 |
rs183803209 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102281665 | AATATAACCACTGTG[C/T]ATGATTTACAGCCTT | 51366 |
rs183810134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102402394 | AGAAACAAAGCCACT[A/G]CTACAACATAAGAGA | 51366 |
rs183816049 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102386662 | TATGACATTCTGTTT[C/T]TATCTACAAATATTT | 51366 |
rs183821595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102371481 | AGTTACAATGTTAAA[C/T]CTGACGCCCCATCAA | 51366 |
rs183839321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102281926 | ACTTTGAGAATCACT[C/T]CATTAAAATGACACC | 51366 |
rs183848634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102379624 | TTATCTCCACTTTCT[C/T]TCCTTTCCATCAAAA | 51366 |
rs183854139 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102345246 | GGCTCTTCAAAATAA[A/G]AAATAATTAATTTTA | 51366 |
rs183887396 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102354859 | GCTGGCCGGGCATAG[C/T]GGCTCATGCCTGTTA | 51366 |
rs183921403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102409993 | CTTTCTATTTTTCAA[A/G]TATCTGCCACCTTGA | 51366 |
rs183927866 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | UBR5 | GRCh38.p7 | 8:102317756 | ACTTCCAGAGGAACG[A/T]TCAGACAGCAGCATT | 51366 |
rs183931208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102378233 | GTGTGGTATCACAAC[C/T]ACCACAATAAAGGCT | 51366 |
rs183933118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102308744 | AGCCTAAGGCAGGTC[C/T]TTCAGGAGGTATTAC | 51366 |
rs183938684 | snp | A/T | 0.00229766 | 0.0338164 | intron-variant | UBR5 | GRCh38.p7 | 8:102326496 | CAAGGGAAGAAAGTG[A/T]TTCTGAAGAGAAACG | 51366 |
rs183947835 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102342931 | GGTTTTAGAGTGGAA[C/G]TGCTTTATTTTGAAG | 51366 |
rs183954178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102384037 | ATCTAGCCAATACAA[C/T]GTACAGCCAAAAAAT | 51366 |
rs183957071 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102268193 | CTTGCCTCAGCCTCC[C/T]GAGCAGCTAGGATTA | 51366 |
rs183970621 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102287350 | CCCTTGCGTATATCA[C/T]ACAAAGTATGACCCA | 51366 |
rs183994260 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102341685 | ACCCAAATGGTTCTG[C/G]AAATAAGAAGAAACA | 51366 |
rs183996751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102316711 | CCTCTTGAGTACATT[A/G]ATCTGTAAAACCCTT | 51366 |
rs184018294 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102358071 | GAATTGCTTGAACCC[A/G]GGAGGCGGAGGTTGC | 51366 |
rs184022044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102263864 | AAGTATAGCTGGGAC[C/T]ACAGGTGCATGCCAC | 51366 |
rs184029235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102260079 | GACATTAACATAGTA[A/G]GATTGATGTTACTCT | 51366 |
rs184057403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102375711 | TTAGGGAAATGTGCT[A/G]CAGGGACCAAAAGGA | 51366 |
rs184074618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102299078 | AGCACATAGACAATA[A/G]GGTACACTGCCTATG | 51366 |
rs184083914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102371049 | GATTCCCTATCTTGG[C/T]TATTGTGACTAGTGC | 51366 |
rs184090568 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102391928 | CACCAAAATCGAGAG[A/G]GCAATGTAAGTGACC | 51366 |
rs184099217 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102336749 | GGTTTTGATTGCTTA[C/T]AGCTTTGTAATACTA | 51366 |
rs184176437 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102273941 | CTTATATCCATTCTT[C/T]TGTAGAGTTCACTCT | 51366 |
rs184215607 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102345874 | AAGACCATCCTGGCT[A/G]ACATGGTGAAACCCC | 51366 |
rs184218580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102371344 | CAAACTCCTGGACTC[A/G]AATGATCCTCCCACC | 51366 |
rs184253096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102312932 | AAGGTGCTGACTTTT[C/T]TAAGTTATTTGATTT | 51366 |
rs184255944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102401624 | TCATTTCTGTTTCTG[C/T]ATCCCCTAGGCAGTG | 51366 |
rs184273485 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102369485 | TATCAATCTACAGTG[C/T]CAAACTCACAGTAAT | 51366 |
rs184292900 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102254662 | AAAAAGGAAAGGGAT[C/G]ATTCATACCTCAAGA | 51366 |
rs184300399 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102397996 | ATTTATATGGAACCA[C/G]AGAAGACCCAAAATA | 51366 |
rs184303727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102385204 | CCACTTTGGATGAAG[A/G]GATCAAAGGTGAATC | 51366 |
rs184399669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102290415 | CACTAGAACTATAAG[C/T]AACTGGTAAAACAGA | 51366 |
rs184400767 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102267837 | AAAGTTTCAAACTGG[A/G]TATCAGATTAGCCCC | 51366 |
rs184405146 | snp | C/T | 0.00209607 | 0.0323054 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102286574 | ACTTGAGTCATTCGA[C/T]TGAGAATCATCTTCA | 51366 |
rs184406099 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102355313 | TCTCTGGGGACAGTC[C/T]CTTTCATATTGCATT | 51366 |
rs184413946 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102331808 | TCTCTACTGGTCTTC[C/T]ACCTACCTTCCATCT | 51366 |
rs184416203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102386378 | AAGGTTGCAGTTAGT[C/T]GATCACAGCACTGCA | 51366 |
rs184454679 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBR5 | GRCh38.p7 | 8:102259829 | ACTTTGGGAGGCCAA[A/G]GTGGGCAGATCATGA | 51366 |
rs184481200 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102355690 | ATCACTGGCATCAAG[G/T]TGGTCAGGAGGCACT | 51366 |
rs184527316 | snp | A/C/G | 0.000616656 | 0.0175487 | intron-variant | UBR5 | GRCh38.p7 | 8:102293875 | AAATATCAGCAATCT[A/C/G]TCTTTTCATATACAT | 51366 |
rs184536950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102368820 | TGCATATAATATTAT[C/T]TAACACAGTTGCCTC | 51366 |
rs184543244 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102334440 | GGGACTACAGGTGCA[C/T]GCTACCGCACCTGGC | 51366 |
rs184592768 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102276756 | AACAAATATTTGTTA[C/G]ATAAACAAAGAACCT | 51366 |
rs184629563 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102273739 | AAGCAGCTATAAAAG[G/T]AAGGTAGAACATCTC | 51366 |
rs184645917 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | UBR5 | GRCh38.p7 | 8:102289035 | ATGGGTGTGGTGGTG[A/C]GCGCCTGTAATCCCA | 51366 |
rs184672244 | snp | A/G | 0.00636936 | 0.0560724 | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102252970 | GAAGAAAACAGTGTT[A/G]TTATGCCACTGAATA | 51366 |
rs184717306 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102414006 | TAAACCCCACTACTC[A/G]GGAAGCTGAGGCAGA | 51366 |
rs184733379 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102376930 | AAATACACACAAGGA[G/T]TAAAATATTCACAAA | 51366 |
rs184739522 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102359811 | AATGAAATAAATGGC[A/G]TGACATTATAAACAT | 51366 |
rs184740380 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | UBR5 | GRCh38.p7 | 8:102396892 | TTTGTATTTTTAGTA[C/G]AGACGGAGTTTCACT | 51366 |
rs184770689 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102325846 | ATCTCTTAATGTCAG[A/C]CTTAATAAAAGACAG | 51366 |
rs184807146 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102286044 | CTACAGACATTCTTG[G/T]TTATCACAACTGTGG | 51366 |
rs184863349 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102350724 | ATCAAACTTTAAAAC[G/T]CTGTGTATCAAAGGA | 51366 |
rs184876182 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102384689 | AAATTTAGGGACAAG[A/T]CTCTTTAAAAACCAA | 51366 |
rs184916576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102267510 | CTCACAAAAATCTTT[C/T]CACCAAAAATGTACA | 51366 |
rs184917003 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102312039 | TAGGGAACAAAAAAA[A/G/T]GCCAATGCCCTGAAT | 51366 |
rs184923092 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102307616 | TGCTCAAAAAAGTTG[A/C]TGATATTTATCTTCA | 51366 |
rs184929287 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | UBR5 | GRCh38.p7 | 8:102331052 | TACTAAATGTATGTT[A/C]TTTTCCTTATGATTT | 51366 |
rs184937572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102345651 | AACTAGGGAATGACA[C/T]CGCCTGAGGAAAAAC | 51366 |
rs184941431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102369074 | AAAATATTTGACAAG[A/G]GGGGCTGTTTTACAT | 51366 |
rs184957519 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102273836 | GGGAGGTGGGAGGAG[A/G]TATGTAATTAATACA | 51366 |
rs184961135 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102289704 | AAATCTGAGCTGAGA[A/G]TTCTTAGAAACCAAC | 51366 |
rs184967221 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | UBR5 | GRCh38.p7 | 8:102393857 | ATTGCTTGAACCAGG[C/G]AGACGGTGGTTGCAG | 51366 |
rs184972494 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102379980 | TTTAGTAGAAAACTT[C/T]GTAACTGAAAATTTT | 51366 |
rs184976190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102397249 | AGATCCTTCTTCCCT[A/G]TCACTTATATATCAA | 51366 |
rs184978794 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102364475 | GCATGGGACATAGTG[A/C]CCAGCCTCAGTCCTG | 51366 |
rs185042621 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102308336 | TAACCCTCTTGCTTC[A/G]TCTATTTGATACCCT | 51366 |
rs185063952 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102396478 | GGCCTGTCTGTGGTA[A/C/G]GTACACAGTATCTTT | 51366 |
rs185108510 | snp | A/G | 1.64868e-05 | 0.00287109 | UBR5 | 8 | allele_origin=G(germline)/A(somatic) | 8:102342632 | ACGTAAACGTAAAAC[A/G]GATTCACGTTCACGC | 51366 |
rs185112684 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102376538 | GAGACGGAGTCTCGC[A/C]ATGTTGCCCAGGCTG | 51366 |
rs185138736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102407551 | AGATGGATCACCTGA[A/G]GTTAGGTTCAAGAGC | 51366 |
rs185169434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102259195 | TATATTATTAAAGCA[C/T]AAGACATAATTTTAG | 51366 |
rs185184864 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102359387 | TGCAATGCCTCAGAC[A/G]TGTAATCCCAAAACT | 51366 |
rs185217157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102390105 | CTTTCTATTAATTTA[C/T]ATCTATGAACTTCCT | 51366 |
rs185219046 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102326010 | TGAAAGGGTTGAGGA[A/G]AAGGCAGGGGTCTCT | 51366 |
rs185220094 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | UBR5 | GRCh38.p7 | 8:102304612 | AATTCAAAAAAAAAA[A/C]CACATTATGAATTAC | 51366 |
rs185222105 | snp | C/G | 0.0448719 | 0.142907 | intron-variant | UBR5 | GRCh38.p7 | 8:102322879 | CTCACTCATAGATGG[C/G]AACTGAACAATGAGA | 51366 |
rs185233193 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102338112 | TGGCTAGAGAAGGGT[A/G]AGTAAAGGGAGCGGG | 51366 |
rs185241607 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102265670 | ACTGTTTCCCTATAG[G/T]TAAAGAACCATTCTT | 51366 |
rs185253607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102283194 | GAAGTACTGATGTAT[A/G]CTAAATATAGATGAA | 51366 |
rs185278876 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102373431 | AAAAAAGTGTAGCAT[A/C]CGACCAAAATTTCAA | 51366 |
rs185285585 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102264208 | GTTTGCAACAGGACG[C/T]AGGTCTGTCAGACCC | 51366 |
rs185289423 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102356041 | TTTAAGAGGATTTAA[A/G]CCTAAGACAATTTGA | 51366 |
rs185359448 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303851 | TAAATTATTTCAAAT[A/T]TATTAAGTGTCCCAG | 51366 |
rs185372960 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102390881 | AACAAAACGTACATA[C/T]ACGTCAGTGAGAAAC | 51366 |
rs185466007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102310640 | AAGCGTGAGCCACCA[C/T]GCCCAGCCTACATTA | 51366 |
rs185468409 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102261082 | AATATACTTAGCTAG[C/T]TTACCACACATTAAG | 51366 |
rs185473691 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102282744 | CTAAGAAGATATACG[A/C]GTGGCCAGTTAGCCC | 51366 |
rs185511225 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102356386 | ACCCAGAAGCAGAGG[C/T]TGCAGTGAGCTGAGA | 51366 |
rs185533055 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | UBR5 | GRCh38.p7 | 8:102388045 | ACGCTCTTTTTCACA[C/T]TCACACAAAAGATCC | 51366 |
rs185535580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102408218 | TCGTAATGTTTTCCG[C/T]AGAATCCACATTATA | 51366 |
rs185541286 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102374089 | ATAGAACTACCACTT[A/G]TCTAGCAGTGATGCT | 51366 |
rs185553540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102338696 | ATTACTATATCTATC[C/T]ATATGAGAAAACCAA | 51366 |
rs185572633 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102404611 | CATACCGGAGGTTAA[C/G]AAGTTATAGCACTGA | 51366 |
rs185589721 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102253477 | TTCAATAATCATGAT[C/T]TTATAAAACATTTTA | 51366 |
rs185639872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102386869 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 51366 |
rs185641752 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102413156 | CGCAGTTGTATTTAT[A/G]GTGAAGTTGGTAAAA | 51366 |
rs185649500 | snp | G/T | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102355785 | GGCAGAGAGAACAGA[G/T]GCACAAAGAGGGGTT | 51366 |
rs185760678 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBR5 | GRCh38.p7 | 8:102317396 | GGGGGAGGGGCGCCC[A/G]CCATTGCCCAGGCTT | 51366 |
rs185764339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102336308 | ATATTTTTTCACAGT[C/T]TATAGAGTGCCTTTT | 51366 |
rs185768351 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102402692 | GACACAGTTAAGGCC[A/G]TCTCTGGAGTTCCAG | 51366 |
rs185769745 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102288568 | AGCTGGGCATGGTGC[A/G]TGCCTGTAGTCTCAG | 51366 |
rs185771866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102335348 | AAATCTAGAGCTGCA[A/G]TTGTTATGTCATGAG | 51366 |
rs185776629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102337635 | CCACCTGGTCGTGAT[A/G]TATATCTTTTTGATA | 51366 |
rs185778104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102309529 | AGAGCAACTTTCAAT[C/T]TTCTAAGCTTCATTT | 51366 |
rs185780848 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102372477 | ATGCTTATGAAGATG[A/C]TAAATGCCAGTTTAT | 51366 |
rs185782093 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | UBR5 | GRCh38.p7 | 8:102377660 | GCAGCGAGCAGAGAT[C/T]GCGCCACTGCACTTC | 51366 |
rs185785885 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102262298 | TATTTTGAAAAAATA[A/T]AAAGCCAAAAGCATA | 51366 |
rs185789946 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102359976 | CACTCCATCACTAGA[C/T]AGAATATTGAAGATG | 51366 |
rs185790173 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102281053 | AGATGATAATCAGGC[C/T]AGGCCAAACTATCTC | 51366 |
rs185792261 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102297056 | ATAATAATTATTTCT[A/G]GTATTTTCTAGAACA | 51366 |
rs185797787 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B, nc-transcript-variant | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102251937 | ATGAATCTTACAACA[C/T]ACAGAAGCATGGAAA | 51366 |
rs185806931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102270284 | ACCAGAGCATATAGG[C/T]TGTTCAGTTATGGTA | 51366 |
rs185812799 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102317048 | TTTGAGGTACCGGGT[A/T]CATCTCACTAGGGAG | 51366 |
rs185815437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102408882 | GGTGGACCTCAGCTG[C/T]CTCTCAGTAGTTGTA | 51366 |
rs185820267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102391113 | GGTTGATGCTGCAGC[A/G]TACAGTGATGGTGCC | 51366 |
rs185875784 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102314977 | TTTTATTAAACTATG[G/T]ATTTATATTAATTTT | 51366 |
rs185947271 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102347326 | GAGCACTGGTTATTC[A/T]CAAGTACAAAGTACA | 51366 |
rs185947521 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102381741 | AATTATAAGAACAAA[C/T]ATAATTTTACCAACT | 51366 |
rs185949680 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102403625 | AAACTACCCAAATTT[A/G]TATCAGCTAGAAAGC | 51366 |
rs185997732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102292157 | GATATACACCTTCTA[C/T]AATCCAAGACAAGTG | 51366 |
rs186013689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102290608 | ATCCACAAGAACTAT[A/G]GGCCCCTCAAAGTGG | 51366 |
rs186030025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102313310 | ATTCTACAACTGCAA[A/G]TGCATTTTAAATATG | 51366 |
rs186052602 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102274210 | ATCATTTTGTTAGTG[A/G]TAGTGTTGATGTTAT | 51366 |
rs186058611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102255055 | ATGCATCAAAATTCA[C/T]GCAATAAGCCATATT | 51366 |
rs186065928 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102333540 | ACTGTTAAAAATATG[A/G]GACATGAAATAGCGG | 51366 |
rs186071282 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102344438 | CCTGCCTCAGCCTCC[C/T]GAGCAGCTGGGACTA | 51366 |
rs186084739 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102366614 | TAAGATAGTTTCCCA[C/T]ATAACTCTTAAAAGA | 51366 |
rs186086800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102398854 | CAATACACAAAATGG[A/G]AGAAAATATTTACAA | 51366 |
rs186091253 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBR5 | GRCh38.p7 | 8:102362209 | TACTGAACAGATTTA[A/G]AAAAACCCCAAAGGG | 51366 |
rs186116931 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102296815 | TAAAACATGACTTAG[G/T]ACAGATTATTTCCAT | 51366 |
rs186127783 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102392278 | GCTCTGCCTATGGAG[C/T]AGCCATTCTCCATTC | 51366 |
rs186134210 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBR5 | GRCh38.p7 | 8:102378500 | AATACAAAAATTAGC[C/T]GGGTGTGGTGGCGCA | 51366 |
rs186162316 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102365563 | TTTGGTGAGGTGGTT[G/T]TAACACACAATGAAT | 51366 |
rs186181234 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102304875 | TTACATATCCAGTTT[A/G]TATATATCATATAGT | 51366 |
rs186192153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102395180 | CAACACTTCTTCAGG[C/T]AAGCTTTTCCCCTGC | 51366 |
rs186244151 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102280244 | CAAGAATGTGTAAGC[A/C]AAAATGGACAGAAAA | 51366 |
rs186318234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102333118 | CCCTGAAAACCCACT[A/G]TGGACAAATGAAGAT | 51366 |
rs186327327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102346627 | GGTGTGGTGGTGCAC[A/G]CCCATTAATTCCAGC | 51366 |
rs186333870 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102346038 | TGCACTCCGGCCTGG[A/G]TAACAAAGCAAGGCT | 51366 |
rs186341955 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102323659 | AGCACCACCTTAAAG[G/T]TCTTCATTAAGAAAA | 51366 |
rs186347664 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102365969 | GCCTAACTCTAACAT[A/G]TAACATATCTGCATG | 51366 |
rs186353424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102291500 | CTTCTGTCCCCCTCA[C/T]ATATATAAAGCTAAA | 51366 |
rs186366644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102314618 | AAAAAAACCAAAGTA[A/G]TAGAGATACAAATTA | 51366 |
rs186366984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102287927 | ATTATTTTAGTTTTT[A/G]AAAGTCTTTTAAGAA | 51366 |
rs186374852 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102414158 | TTTTTCCCTAAGGAA[A/C]CAATTCATGACTTTC | 51366 |
rs186381039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102395457 | AGTGTATTCATATTT[A/G]TAATTACATATATAC | 51366 |
rs186386612 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102381138 | GGGAGGCCAAGGCAG[A/G]TGTTATCACTTGAGG | 51366 |
rs186445262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102265009 | AGCCACCGCACCCAG[C/T]GTACATACATTTTAA | 51366 |
rs186465008 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102328204 | CAGGTGTCATGCCTG[C/T]AATCCCAGCACTTTG | 51366 |
rs186476187 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102385747 | TCCAATTAATCACTT[A/C]CTGCTTTGAAGTGTC | 51366 |
rs186575525 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102268486 | TGGGATTACAGGTGA[A/G]AGCCACCGCACCCGG | 51366 |
rs186584572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102267156 | GTACTAATGCAGTAT[A/G]AGCAGAGAAGTTGGT | 51366 |
rs186618445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102340450 | ATCAAGCCTTCCCCC[A/G]AAACCTTTTGCTCCT | 51366 |
rs186632217 | snp | A/G | 0.00273602 | 0.0368853 | intron-variant | UBR5 | GRCh38.p7 | 8:102285357 | TGAAGACCAAACTAA[A/G]ATAGTTAAAACTATC | 51366 |
rs186632419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102375464 | CACAACAAAGGAATG[C/T]TGTCCTGCAAAATAA | 51366 |
rs186646377 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102306931 | AAAAATTTCTTGTGG[G/T]TCTACTGTGTGGTAG | 51366 |
rs186649062 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | UBR5 | GRCh38.p7 | 8:102325409 | TAGATGAAGAAATTA[A/C]CACCACATTCTATAA | 51366 |
rs186660455 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102343128 | TCGAAAAATGCACAC[A/C]TAGAAAAAACCCTAA | 51366 |
rs186668633 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBR5 | GRCh38.p7 | 8:102389665 | CATTGGTATATGACT[A/G]AAGACTCATTTATGC | 51366 |
rs186677837 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102279287 | AACAGACCTTTAACC[C/T]GCTCAATCCAAAATT | 51366 |
rs186691312 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102370324 | AGCACACGCCACCAC[A/G]CCTGGCTAATTTTTG | 51366 |
rs186712592 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102399362 | TTACTGCAACCTCCA[C/T]CTCCCAGGTTCAAGT | 51366 |
rs186736663 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102343555 | CATAGGATGAACATA[C/G]GAAAAGAGACATTTG | 51366 |
rs186738478 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102409184 | CAGCATTCTGTGCCA[A/G]GCACCTTGTAATCAT | 51366 |
rs186838952 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102260685 | AAATGATTGTTTTAG[G/T]GTCCTACCGCTAATA | 51366 |
rs186885215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102328475 | ACTTTAAAGCCAAAT[C/T]GATAATTTGAGACAT | 51366 |
rs186895564 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102406948 | ACACTTTCTATGCCA[A/G/T]CACTATCCAAGAGAA | 51366 |
rs186899995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102390051 | GGCGTGAGCCACCAC[A/G]CCCAGCCAAGAAGGA | 51366 |
rs186908213 | snp | A/G | 6.61288e-05 | 0.00574979 | intron-variant | UBR5 | GRCh38.p7 | 8:102295591 | ACTCAGCTGTGCTGC[A/G]CTCTTTTGATTTAAC | 51366 |
rs186911474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102375827 | GTCTAAGCGCCTTAC[A/G]TTGGTAACAGGAATC | 51366 |
rs186929195 | snp | A/G | 0.000826105 | 0.0203069 | intron-variant | UBR5 | GRCh38.p7 | 8:102361673 | ACAGATCTTTTGTAA[A/G]CAAATACTTCTGACA | 51366 |
rs186949430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102266054 | TTCATTCAGCTATTG[A/G]TGCATCCTGTGAATT | 51366 |
rs186951193 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102332859 | CTATATTACCATATG[A/C]CAGCTTGGTATATGG | 51366 |
rs186964928 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102391697 | TAAATGTTTTCTTAT[A/G]AAAGGGAGGGGGGAA | 51366 |
rs186983599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102315195 | GCAAACAAGTTTCAC[A/G]CTGCAACACTGCTAA | 51366 |
rs186994281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102334144 | AGAGCTTAAACAAGG[A/G]GTCAAATGAAATGGA | 51366 |
rs187007042 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102276243 | AGCATGGTTAAAACT[A/T]AATATGGCTTCTTCA | 51366 |
rs187008679 | snp | A/G | | | intron-variant, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102258644 | ACATGAATCAGAAAA[A/G]CCCAGAGAGTTGTCA | 51366 |
rs187011487 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102335704 | CAGGCATGTGCCACC[A/C]TGCCCAGCTAGTTTT | 51366 |
rs187026970 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102369740 | AGGTATAGATTTAAT[A/G]CAGTTAATAACTCCT | 51366 |
rs187027584 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102293092 | AATATTTGCCAAAGA[G/T]CTACAGCATTATTAC | 51366 |
rs187103468 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102337066 | ATTATTTTCTTAATT[C/T]CTTTTCCGGCTAGGC | 51366 |
rs187112130 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | UBR5 | GRCh38.p7 | 8:102355606 | TTTTTCATACAGCCC[A/T]AGAGAAACAATCAGA | 51366 |
rs187139898 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102371389 | AGCTGAGACTATGGA[C/T]GCATTCCACCATGGC | 51366 |
rs187141559 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102411523 | CTCAAATTTAATAAT[A/C]ATAACAATAATCATG | 51366 |
rs187147711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102284160 | GCTGATACCTACTCC[C/T]GAAAAAGGTCACTTT | 51366 |
rs187148202 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102393204 | AACTTTAAGTCAATT[A/T]TTTTTAAATGACTTA | 51366 |
rs187152978 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102319038 | TGCATCAACTAACGA[A/G]CAAAATAACCAGCTA | 51366 |
rs187188027 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102283057 | TCTATACACAAAAGT[C/T]CATATGAGCATTATG | 51366 |
rs187199028 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102255905 | GTTCACAAACTAAAG[C/T]TGTTGACAGGAAATT | 51366 |
rs187215188 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102317256 | ACTGCGCTTTTCTGA[C/T]GGGCTTAGGAAATGG | 51366 |
rs187222429 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102385325 | GAAGTTCATGTATAA[A/C]TTGTTCTGTATTTCA | 51366 |
rs187225283 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | UBR5 | GRCh38.p7 | 8:102352703 | TACAAGCCTGATCAG[A/C]AATAGTATCCAAGTA | 51366 |
rs187236027 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102410524 | ATAACAAAATGTTAA[A/G]TAACTAAAAAGTTAT | 51366 |
rs187417630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102304379 | TTATTTCCTTATTCC[A/G]CCTTCCTTCTCAATC | 51366 |
rs187482326 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102354161 | TGAAAATATCAATTA[A/G]TCCCAACATTTAAGA | 51366 |
rs187482555 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102310834 | GAACACACAAACACC[C/G]TAGTGCCCCTCTCCA | 51366 |
rs187488662 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102330836 | GGGTAAAAACCAAAC[A/C/G]GAGTAACATATATAG | 51366 |
rs187500402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102273746 | TATAAAAGGAAGGTA[A/G]AACATCTCATATTTT | 51366 |
rs187504301 | snp | A/C | 0.00358779 | 0.0422022 | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102252998 | ATAAAGCTACTTAAA[A/C]CAGAGTAATTTTGGG | 51366 |
rs187505592 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102370716 | TAACCAACCTGTCTT[C/G]ATCCTACCTTCCCCG | 51366 |
rs187507718 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102289037 | GGGTGTGGTGGTGCG[C/T]GCCTGTAATCCCAGC | 51366 |
rs187513732 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102336597 | CCAGTTTTCCCAGTA[C/T]CACTTATTGAAGAAA | 51366 |
rs187519982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102275320 | GTGGTTACAATAAGA[A/G]AAAAATAAAAAGAAA | 51366 |
rs187533003 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102399700 | ACCTGTAATCCGAAC[A/T]CTTTGGGAGGCCAAA | 51366 |
rs187539940 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBR5 | GRCh38.p7 | 8:102328868 | GCCTCCCAAAGTGCT[C/T]GGATTACGGGCGTGA | 51366 |
rs187561999 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | UBR5 | GRCh38.p7 | 8:102274547 | GACCAGCCTGGCCAA[C/T]ATGGTGAAACCCTGT | 51366 |
rs187564355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102288633 | ACCCGGGAGGTGGGG[A/G]TTGTAGTGAGGCAAG | 51366 |
rs187572139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102282146 | TGCACTCCGGCCTGG[A/G]CAACAGAGCGAGACC | 51366 |
rs187573247 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102263885 | TGCATGCCACCACAC[A/G]CAGTTAACTTTTAAA | 51366 |
rs187597210 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102384102 | GCATATCAACAAGAG[A/T]AGGGACAAGCCTTTT | 51366 |
rs187602547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102406526 | CTCAAACTTCTGACC[C/T]CAGATGATCCGCCCA | 51366 |
rs187617740 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102405137 | GGGCAATTTTGTTAT[C/T]AAGGTTTTTTCAGGT | 51366 |
rs187749499 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102272902 | AAACAACAAAGTAAT[G/T]GGAGTTCTCAGAAGC | 51366 |
rs187792552 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102267759 | AGGAGTGTATCTAAT[C/G]TAAATTCCTAACTCA | 51366 |
rs187805266 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | UBR5 | GRCh38.p7 | 8:102308209 | TCTTCACATTCACTT[A/C]CTCTATCAGAAGAGA | 51366 |
rs187810623 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102284774 | GGGCGCTGTGGCTCA[C/T]GCCTGTAATCCCAGC | 51366 |
rs187811108 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102256773 | TTCCCCTCCTTCCCT[A/C]CACCACCCCCAAAAT | 51366 |
rs187837302 | snp | C/T | 0.111224 | 0.207945 | intron-variant | UBR5 | GRCh38.p7 | 8:102396651 | ACACATATATATATA[C/T]ACACACACACACACA | 51366 |
rs187853167 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102266886 | CTTTCATCCCCTTTA[C/T]TGAAATTTCCTTGTA | 51366 |
rs187853920 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102367104 | TGTGTACTATATAGA[C/T]GGTAGAGACAAGCAC | 51366 |
rs187870166 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | UBR5 | GRCh38.p7 | 8:102341910 | ATACAGAGCATAACT[C/T]CCCTAGCCCATTCCT | 51366 |
rs187905888 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | UBR5 | GRCh38.p7 | 8:102396947 | TCCTGACCTCGTGAT[C/T]TGCCCATCTCGGCCT | 51366 |
rs187993130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102349021 | CACTACCAATTCATG[C/T]TTATGCAGTATCTGT | 51366 |
rs188029753 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102315788 | CAATGACTGGCAAAC[A/G]AGGGTACTACTGACA | 51366 |
rs188033710 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102334354 | TGGAGTGCAGCAGCA[C/T]GATCTTGGCTCACTG | 51366 |
rs188038611 | snp | G/T | 0.00358779 | 0.0422022 | utr-variant-3-prime, downstream-variant-500B | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102252289 | TTATTTTACATGTCT[G/T]TATTTTACATTTAGA | 51366 |
rs188068673 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102252497 | TTGTTCTCATTTAAT[A/G]TTTTATCAATCCCAT | 51366 |
rs188072298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102286119 | TCTAGTGGGTGTAGG[C/T]TAGGGATGCTGCCTA | 51366 |
rs188081697 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102363001 | GAATTACAGGTACCC[A/G]CCACCACACCCGGCT | 51366 |
rs188084661 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102348143 | GAAGAACTGCTTGAA[C/T]CAGGACCCAGGAGGC | 51366 |
rs188107169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102330291 | GATAAACAAATGGTG[C/T]CTTTCTGGTTTTTCT | 51366 |
rs188117802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102358945 | ACATTCAGCTACATT[C/T]TTGTATTTTTAGTAA | 51366 |
rs188125908 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102382270 | AGGAGGTCAGGGAGA[C/G]GAGACCAACAGAATC | 51366 |
rs188144401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102325908 | CTGTTGATACCTTCT[C/T]CTGACAAAGCTAATT | 51366 |
rs188146933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102386385 | CAGTTAGTCGATCAC[A/G]GCACTGCACTCCAGC | 51366 |
rs188149410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102259967 | CAGGAGGCGGAGGTT[A/G]CACTGAGCCAAGGTT | 51366 |
rs188260663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102287743 | GACTAAGTAACTACT[C/T]AACCTTAGAAGAATG | 51366 |
rs188301752 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102281837 | AGAGTTTTAGTAGGT[A/C]TGGGGTAAAGCCCCA | 51366 |
rs188310674 | snp | C/G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102308844 | TTAATACCTGGGTGA[C/G/T]GAAACAATCTGTACA | 51366 |
rs188310866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102390938 | AAAGACAATGAATAT[C/T]GAGGCTGGGTGTGGT | 51366 |
rs188322828 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102377112 | AATCTTATGCTTCCC[A/C]AGTTGAAGCTGAACA | 51366 |
rs188323529 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102273580 | GTCTAAGAATCTATC[C/T]CAGGGACACACTAGC | 51366 |
rs188324629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102328149 | GTCAGAAGTAAACAT[C/T]TGCTCTACCAATTTT | 51366 |
rs188329170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102359860 | TTTTTTAAAGGTCAA[A/G]AGCCTAGATTAATTG | 51366 |
rs188330843 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102310180 | CAGAAGCTTTATTAA[G/T]TCTTTCATTCACTGC | 51366 |
rs188330997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102342988 | TTAAATTGTTGGCTT[C/T]CATTAGAAATGCGTA | 51366 |
rs188348731 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102345303 | TAATAACTGTAATAT[G/T]AGAAGTTCAAATACA | 51366 |
rs188349532 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102408376 | TTGAAACTCCTGTCT[A/G]TAGTATCTTACCTTG | 51366 |
rs188362699 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102317618 | CAGCTGGAGATCTGA[G/T]AACGGGCAGACTGCC | 51366 |
rs188375111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102260261 | AATGCAGTTCAAGAT[A/G]AACATGTGCTTTCTT | 51366 |
rs188391878 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102379682 | AAAAAGGAAAAAAAT[A/G]TAAGAAACACTTCTT | 51366 |
rs188399960 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102335047 | AAAACACACACACAC[A/G]GACACAACAGAAAAA | 51366 |
rs188403017 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102344855 | AATCTCTTGAACCCA[A/G]GAGGTGGAGGCTGCA | 51366 |
rs188410192 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102350873 | TAGCCTAATTAAAAA[A/C]TGGGCAAAGGACGTG | 51366 |
rs188419752 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102401704 | TTCTATTGGCGACTA[C/T]AGGAGGCAAAAAAAA | 51366 |
rs188424448 | snp | A/C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, nc-transcript-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102413001 | TGCGGGCTAACCTGC[A/C/T]GGGAGGGAGGGTAAG | 51366 |
rs188428502 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBR5 | GRCh38.p7 | 8:102277722 | TTCTTGGCCTGAGCG[C/T]GGTGGCTCACGCCTG | 51366 |
rs188430213 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102369095 | TGTTTTACATTTTTG[A/C]AAACCTCTTTATTAT | 51366 |
rs188432395 | snp | A/C/T | 6.63552e-05 | 0.00575967 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295221 | GTCTTTATTCTCCTG[A/C/T]GACCCAAACATAATC | 51366 |
rs188438703 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102316871 | ATCTAATAACAAAAC[G/T]AGGGCATCAAAAGAG | 51366 |
rs188564869 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102263536 | TAATTTTAAAGCAAA[C/T]GGTTTTTCTTTTCCC | 51366 |
rs188587702 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102299604 | AACATATTCCTAACA[A/T]GTTCTCTTAACTGGC | 51366 |
rs188607531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102264055 | CTCTTTTCAATACCA[C/T]TACCTTCTCTAACAC | 51366 |
rs188619432 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102409003 | CTCTCCCCTCAAGCT[C/T]GACGAACCACATTCT | 51366 |
rs188627747 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102391608 | TCTTAGTAAGTTAGG[C/T]AGGAATATCATCACC | 51366 |
rs188634585 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102371067 | TTGTGACTAGTGCTG[C/T]GATAAACATCTCTTA | 51366 |
rs188639576 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102297921 | CAAATTATAGACCAT[C/G]TCATAAACTATTTAT | 51366 |
rs188653801 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102336759 | GCTTATAGCTTTGTA[A/T]TACTATTTTAAACCA | 51366 |
rs188660557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102393411 | GGAGGCCAAGATGGG[C/T]GGATCACGAGGTCAA | 51366 |
rs188669368 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102401336 | AGAGCAGAGAGACCC[C/T]AGAGAAAAGCAAAAT | 51366 |
rs188671028 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102282402 | GGTCAGGCGCAGTGG[C/T]TCACACCTGTAATCC | 51366 |
rs188673215 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | UBR5 | GRCh38.p7 | 8:102254964 | AATAATAAAATAATA[A/C]AGCAAAAAAAGTATT | 51366 |
rs188675353 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102302214 | AAAAACAAAAAACAA[A/G]AAACAAAAAAAGAAA | 51366 |
rs188682165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102363411 | CTGTGTTCCAAGATA[A/G]AACACCTTAAGGGTA | 51366 |
rs188828169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102259327 | GAAGTGGGGAGGGAA[A/G]GCATAGTGAATAAGC | 51366 |
rs188842040 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102324155 | GAAGAAACTAAAAGG[C/G]ATTATAATTTAAAAA | 51366 |
rs188855012 | snp | G/T | | | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102413918 | GGGAGTTCGAGACCA[G/T]CCTAGCCAACTTGGT | 51366 |
rs188870346 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | UBR5 | GRCh38.p7 | 8:102318517 | TGGAAAACACTCTTC[A/G]GGATAATATCCAGGA | 51366 |
rs188871322 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | UBR5 | GRCh38.p7 | 8:102394358 | AGCCACCGCATCCGG[C/G]CAGAATTTATTCTTT | 51366 |
rs188904825 | snp | A/C | 8.56905e-05 | 0.00654507 | intron-variant | UBR5 | GRCh38.p7 | 8:102293574 | TTCCAGAGAAGGATT[A/C]ATCAGAATCTGTTAC | 51366 |
rs188921201 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102388512 | ATGAAGCCGAGTGGT[C/T]CTTCTTTTTTTCGTA | 51366 |
rs188939880 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102354882 | GCCTGTTACCTCAGC[A/C]CTTTGGGAAGTTGGG | 51366 |
rs188940661 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102333057 | GAGATAGGGCAATGT[C/T]CCCCACGGTGATAAG | 51366 |
rs188945147 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102346166 | AGAAAAGTCTATTGT[C/G]CTTTAAATTCCACTC | 51366 |
rs188954073 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102385839 | CCCTTAAGGATAAGT[A/C]AGGCCTGTAATTTTT | 51366 |
rs188966222 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102402477 | AAAACTCTGTTTTCA[C/T]CATTTAGAAATTAAA | 51366 |
rs188975256 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102314428 | CAAGACATAATCAAT[A/T]TACAATAATAAGAGT | 51366 |
rs188976485 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102386832 | AATACAAAAATTAGC[C/T]TGGTGTGGTGGCGGG | 51366 |
rs188980826 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102355718 | ACTATGACATTTTAC[A/G]GTATTGCAATCATGG | 51366 |
rs188984858 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102371692 | GTCCCTGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 51366 |
rs189111985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102305358 | GCACATTACATATAT[C/T]AAAAATTTCTCATGG | 51366 |
rs189128036 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102276614 | TCTTACATCGTTATT[A/T]GACAACGTATATACA | 51366 |
rs189139036 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102316114 | AGCAAAACCTTAATG[A/G]GGTATAAAGTGCAAT | 51366 |
rs189161210 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102374969 | GGGGAGCTTAACAAA[C/T]GGACATTCATGTCTT | 51366 |
rs189162724 | snp | C/T | 6.7113e-05 | 0.00579241 | intron-variant, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102276931 | GATATATATTTTTAA[C/T]GCTGTACTGAACAAT | 51366 |
rs189184416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102339586 | CTCTAAATGGATGCT[A/G]GGAAAGTAGGTACTA | 51366 |
rs189349313 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | UBR5 | GRCh38.p7 | 8:102380115 | AAACAGCAAAGAGGC[C/T]GGGCGCGGTGGCTCA | 51366 |
rs189353565 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102312159 | TACATTCACTGCTAA[C/T]ATTTCTGTTTTTTCA | 51366 |
rs189353621 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102265496 | GTCTTTAACGTCTCT[G/T]TTGTTAAAATAAAGT | 51366 |
rs189355944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102331508 | TCCTCCCCTCCTATT[C/T]AAAGATAACCCACAG | 51366 |
rs189359917 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBR5 | GRCh38.p7 | 8:102364527 | AAGCAAGTGTATCAA[C/T]GGAAGATATATACGT | 51366 |
rs189360119 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102283063 | CACAAAAGTTCATAT[G/T]AGCATTATGCATAAT | 51366 |
rs189364300 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102304399 | CCTTCTCAATCCACG[A/G]AGGGCAAAAATAAGG | 51366 |
rs189368578 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102345673 | AGGAAAAACACAACA[A/C]CCTACATTATTAACA | 51366 |
rs189382826 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102413294 | ACTTCTATTACCTCG[A/G]TCTCCCCAGTTTCCT | 51366 |
rs189407062 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102294383 | GAAGAACAATACCAA[A/G]TATATGAAATCAGAA | 51366 |
rs189412982 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102268385 | TTAACTTTTTTTTTA[C/G]TAGAGATACGGTTTC | 51366 |
rs189431184 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102334571 | TGCTGGGATTGCAGG[C/T]ATGAGCCACCAAGCC | 51366 |
rs189466388 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102368911 | CCACCTTATACTCTT[A/C]AAAACTACTGAAGAC | 51366 |
rs189471900 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102369505 | CTCACAGTAATGGGT[A/T]CAAGTTTCCCAAAAT | 51366 |
rs189475323 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102377799 | CTTTAAGTGTGAAAA[C/T]AAAAGATCTTTATGA | 51366 |
rs189487498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102397283 | GCACTTAATTCCTTC[C/T]TTACATGTCTGTCTC | 51366 |
rs189506369 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102398042 | AGCAAAATAACAAAA[C/T]TGGAGGAATCACATT | 51366 |
rs189511294 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102352202 | AGTCTCAGCTACTTG[G/T]GGGGACTGAGGCAGG | 51366 |
rs189515088 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102385261 | AAAAATAAGCACTGA[A/T]AGACATTCAAAATAG | 51366 |
rs189603591 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102286760 | CTACCATAAAATAGT[C/T]TTTATTAGAAAATAA | 51366 |
rs189607936 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102308451 | ATGATGGACCACATA[A/T]ATGACTGTGGTACTA | 51366 |
rs189688107 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102290451 | TGGATTACAAAAGTG[C/G]GAAAGGCTAAGAGAA | 51366 |
rs189713833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102332482 | GCAAACTGTCTAGTC[A/G]TCTCCATCCCATCTC | 51366 |
rs189753533 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102364985 | TAATTATTCTATACA[A/G]CAGAGATTCACCTAC | 51366 |
rs189766997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102384700 | CAAGTCTCTTTAAAA[A/G]CCAAAAGAGCTCTGC | 51366 |
rs189767418 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102362623 | AAAATGTTATACATA[C/T]TCCAAAAATAAATGA | 51366 |
rs189786210 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102329782 | TTTCTTTTTAATCCA[C/T]AGCACTTCACAACTT | 51366 |
rs189787926 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBR5 | GRCh38.p7 | 8:102410560 | AATTTAAAGGAACTA[C/T]GTGACAACTCTGAGT | 51366 |
rs189798796 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102344649 | AAATAGCATTTTAGG[C/G]TGGGCGCAGTGACTC | 51366 |
rs189802822 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102392546 | TAAAGAAAATACAGG[A/G]AAAAAAAAAAGGTAA | 51366 |
rs189806828 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102378501 | ATACAAAAATTAGCC[A/G]GGTGTGGTGGCGCAC | 51366 |
rs189880967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102261423 | AAAAAGGACAAGCCG[C/T]CAGGCGCAGTGGCTC | 51366 |
rs189946575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102282852 | ATAACAAAAGACAGA[C/T]AATAAGTGCTGGTGA | 51366 |
rs189953595 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBR5 | GRCh38.p7 | 8:102312975 | ACAGCCACATATACA[A/G]CTAGTGGCTACAATA | 51366 |
rs189981803 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102273983 | GATATTTTACATTGA[C/T]TACAAAATAAAACCA | 51366 |
rs189999951 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102380349 | CAGGGAACCAAGATC[A/G]TGCAACTCCAGCCTG | 51366 |
rs190013711 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | UBR5 | GRCh38.p7 | 8:102319989 | ACAAGAGAAAGCAGG[A/G]AAGATCCAAAATTGA | 51366 |
rs190022457 | snp | A/C | 0.0240643 | 0.107019 | intron-variant | UBR5 | GRCh38.p7 | 8:102345886 | GCTAACATGGTGAAA[A/C]CCCGTCTCTACTAAA | 51366 |
rs190038587 | snp | C/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102414100 | CAACAGAACGAGACT[C/G]CATCTCAAAAAAAAA | 51366 |
rs190060171 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102380668 | CAACAATGTATATAA[C/T]AAAAACTGACCATTT | 51366 |
rs190097685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102262614 | TTCTTTAAATAAGAA[C/T]ATTTTAGCTGGAACA | 51366 |
rs190111956 | snp | A/G | 1.65603e-05 | 0.00287747 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102281510 | ACGGGCGCTAAGCAA[A/G]GTGGCACGTCTATAA | 51366 |
rs190116293 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102297163 | ATGATATACAAATAG[A/T]AATATTACCAGTAGA | 51366 |
rs190147163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102353915 | GCATGCCTGTAGTCC[C/T]AGCTACTTGAGAGGC | 51366 |
rs190180553 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102385755 | ATCACTTACTGCTTT[A/G]AAGTGTCATCTCTGA | 51366 |
rs190182662 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102317455 | TTGAACTGGGTGGAG[A/C]CCACCACAGCTCAAG | 51366 |
rs190186489 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102370356 | ATTTTTAGTAGAGAC[A/G]GGCTTTCGCCATGTT | 51366 |
rs190190575 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102336483 | TTATATTTTCTCATA[C/G]TTTTTAAGGTTTCAT | 51366 |
rs190206050 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303878 | CCAGCTCTACCTTAA[A/C]CTCTAATTTGTTATC | 51366 |
rs190207629 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102273846 | AGGAGGTATGTAATT[A/C]ATACATACATATGCT | 51366 |
rs190232902 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102264721 | CAAAACAAAACAAAA[A/C]AAAACAGGAACACCA | 51366 |
rs190248763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102337864 | CAACATATTATGAAA[C/T]TTCTAATCTAGAAAA | 51366 |
rs190270652 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102365598 | TAGCAAAAAGCTTCT[A/G]ACAATCCTTGGGTAC | 51366 |
rs190274723 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102337484 | TTTATCAAGAAAGAA[C/T]GCTCAACTTCTTCAA | 51366 |
rs190289652 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102403007 | ATAATCTTTTTACAT[A/G]TACTAGTATGTTTTT | 51366 |
rs190303700 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102373039 | TGGAGAACGGGGTCT[C/T]GCTATATTGCCCAGG | 51366 |
rs190306667 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102395270 | GTCACACTGTCCTGT[A/G]ACTGTCTCTTTTTCA | 51366 |
rs190356872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102283902 | TTTTTTATTTCAATG[C/T]TTCTCTCCCCTCCTT | 51366 |
rs190360970 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | UBR5 | GRCh38.p7 | 8:102256782 | TTCCCTCCACCACCC[C/G]CAAAATAAGCTTCTG | 51366 |
rs190396905 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102356177 | AAATAAGGCCAGGCG[C/T]GGTGGCTGACACCTG | 51366 |
rs190421292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102275453 | AAGCTATTGTTATTT[C/T]GCATGTTTTAAAATT | 51366 |
rs190425656 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102387328 | AATAAAACTTCTGTA[G/T]CGATTATAAAACTCA | 51366 |
rs190425887 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | UBR5 | GRCh38.p7 | 8:102304716 | ACCTTCCAAAAACAT[A/T]TAACACCTCACTAAG | 51366 |
rs190429140 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102322949 | CTGTTGTGGGGTGGG[A/G]GGAGGGGGAGGGATA | 51366 |
rs190432793 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102373863 | TGCCTTTGAAATGGT[A/C]ACTTTACGTCCTAAG | 51366 |
rs190437870 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102338344 | TCACTTTGGTACATA[C/T]AGGCTGCCCTTAATT | 51366 |
rs190443801 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102254045 | AAATCACAGTGTAAA[C/T]TATGTTGTTCTGCTG | 51366 |
rs190444612 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102385827 | ATAGTAAGCTTACCC[G/T]TAAGGATAAGTAAGG | 51366 |
rs190452928 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102371041 | TAAGTTTTGATTCCC[C/T]ATCTTGGCTATTGTG | 51366 |
rs190455921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102290007 | TGCTGATGTGTGTGG[A/G]GAAAACATCAGTTCA | 51366 |
rs190468114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102274381 | AATGAGTAATTTGAT[C/T]AATGTTGTTGGGAAG | 51366 |
rs190470674 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102255877 | AAACATAGATTTTCA[A/G]TAAGAGTTTAAGGTT | 51366 |
rs190481809 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102400226 | GAAGCTGAGGCAAGA[C/G]GGTTGCTTGAGCCCA | 51366 |
rs190502365 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102295878 | ACTCACTGAAACCAG[A/G]GAGAGCCCTTGTTAA | 51366 |
rs190509058 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102355844 | GACTCAGAAAACTAA[G/T]GATTCTGTCTGCATT | 51366 |
rs190527500 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102260795 | CTAAGTGATGGAAAC[A/G]TTTTGGTATAAAAAG | 51366 |
rs190537307 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102291268 | AGGAACACATATATA[A/T]GCTAGATATTAAAAA | 51366 |
rs190542873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102386932 | AGTGAGCCGATATCA[C/T]GCCACTGCACTCCAG | 51366 |
rs190544478 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102390140 | CATTTATTTCAAATA[C/T]TTATTTACAAATCTA | 51366 |
rs190560101 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102359535 | CATTTACAAACTTCA[C/T]TAAACTGATTCAGAA | 51366 |
rs190569076 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UBR5 | GRCh38.p7 | 8:102335605 | CCAGGCTGTAGTGCA[A/G]TGGTGTGATCTTGGC | 51366 |
rs190587795 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102396612 | ACTTAACAGATATAT[A/C]TAAATTCAAATATAT | 51366 |
rs190607400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102366929 | AAAACAAAAATGCAG[C/T]ACATGTAAAAAATCT | 51366 |
rs190695083 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102374338 | CCAGGGAATGAAAGC[A/T]AAGTCTGGGAATTCT | 51366 |
rs190722311 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102404893 | GCCTGGGCAACAAGA[A/G]CGAAACTCCATCTCA | 51366 |
rs190732813 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102388097 | ATAAAAACTGCAAAA[A/T]ACCCAAGAAAAATGG | 51366 |
rs190734709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102279680 | TGTCTGAGCAATTTA[C/T]ATATCTCAATAGTAA | 51366 |
rs190751339 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102342798 | AATTTATGTAAATGT[A/G]TATCTAATAAGGCTG | 51366 |
rs190755648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102317168 | GGGTCAGGTCAGGGA[A/G]TTAGTTCCCTTTCCT | 51366 |
rs190797237 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102366513 | TTTCAGAGGCAGAAA[A/G]TGTTCCTGATCTTAA | 51366 |
rs190798500 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102376655 | ATTACAGGCGCCCGC[C/T]ACCACACCTGGCTAA | 51366 |
rs190800651 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102353205 | GTACTGGAATCAGTT[A/G]ATTCCTTTTATCTAT | 51366 |
rs190821518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102333179 | GGACAAAAAAATCAC[C/T]TACTACTTCTTGCCT | 51366 |
rs190821569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102284775 | GGCGCTGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 51366 |
rs190825230 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102414340 | TTTATGAAAAAATAC[C/T]TACAAATCAGGACAG | 51366 |
rs190825340 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102396109 | GTTAAACTAACCAGA[C/T]GGCAAGAGCTTAGAA | 51366 |
rs190826600 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102252308 | TTTACATTTAGAACC[A/G]TTTTATGATTTACTT | 51366 |
rs190827483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102305605 | ATGCATAAATGAATA[A/G]GAGTGGCTGGATTCG | 51366 |
rs190829862 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102407696 | GAGGTGGACGTTGCA[C/T]TGAGCCGAGATCCGG | 51366 |
rs190831433 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102346691 | ACTCAGGGGACGGAG[A/G]TTGCAGTGAGCTGAG | 51366 |
rs190839492 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102325056 | TGCAACATCCTGCTA[A/G]TACATGAGTGCAATT | 51366 |
rs190839575 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102381238 | AGACATGGTGGTGTG[A/C/T]GCCTATAATCCCAGC | 51366 |
rs190840294 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBR5 | GRCh38.p7 | 8:102385479 | AAGTATAATTAAGGT[A/G]CCACAGTCCAGTAAG | 51366 |
rs190850818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102381891 | TTTCTCACTAATCAT[A/G]GACTGTGAAGATTTT | 51366 |
rs191001850 | snp | A/C | 0.0018432 | 0.0303019 | intron-variant | UBR5 | GRCh38.p7 | 8:102271259 | ACCTAGAAGAAAATC[A/C]GAAATATACTGTATT | 51366 |
rs191007809 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B, nc-transcript-variant | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102251954 | CAGAAGCATGGAAAC[C/T]ACTGCCTCAAGGGAT | 51366 |
rs191037247 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102273139 | GACAAGCTAAGTGGG[C/T]GGGAGGCTGGAGGGG | 51366 |
rs191039699 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | UBR5 | GRCh38.p7 | 8:102335790 | CTGACCTCAGGTGAT[C/T]CACCCGCCTTGGCCT | 51366 |
rs191042306 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBR5 | GRCh38.p7 | 8:102344159 | ATTTCTGTTATCTGA[A/G]TCAAGTAGTTTTACA | 51366 |
rs191042501 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102309035 | TTTTAGATAGCTACA[C/T]AATGTGTGTGTGTGT | 51366 |
rs191051782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102309749 | TGCACTATGTGATGT[C/T]TGTACAACAATGAAA | 51366 |
rs191061034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102288597 | AGCTACTCAGGAGGC[A/G]GAGGCAGGAGAATTG | 51366 |
rs191077780 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102309565 | AAATGCCCTATCAGG[C/T]GCACCTTTTTTTTAT | 51366 |
rs191078343 | snp | A/G | 1.89766e-05 | 0.00308025 | intron-variant | UBR5 | GRCh38.p7 | 8:102296847 | CAGCAATATAAATCT[A/G]AACAGCTTATAATAT | 51366 |
rs191079149 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102268812 | TACATGAGAAGAAAC[C/T]AAGCTGTCTCATTCA | 51366 |
rs191084682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102328539 | CTTCTCAACATCTTT[C/T]CTTAGCAATTTTCTT | 51366 |
rs191084963 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102398926 | GAGCTCAAACAACTC[C/T]ACAAGAAAAAATCTA | 51366 |
rs191094512 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | UBR5 | GRCh38.p7 | 8:102358036 | CTATAGTCCCAGCTA[C/T]TTGGGAGGCTGAGGC | 51366 |
rs191099556 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102370242 | TGTGATCTCAACTCA[A/C]TGCAGCCTCCGCCTC | 51366 |
rs191107867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102343165 | TAAACTATGAATCCA[C/T]TAATATAAGCTAATT | 51366 |
rs191114935 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102406588 | CATGAGCCACCGCAC[C/G]TGGCATAATGCATTT | 51366 |
rs191115118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102325794 | GATTTTCAAAAAAAT[A/G]GTGGCGAGAAAAGTA | 51366 |
rs191119479 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102340549 | ATGGTATTTATCCTG[C/T]GCCCCTGTATAATAC | 51366 |
rs191123385 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102294786 | TTTATGACAGGTTCT[A/G]AGGGCACTGATAGTT | 51366 |
rs191125334 | snp | G/T | 0.021333 | 0.101051 | intron-variant | UBR5 | GRCh38.p7 | 8:102389852 | GCAAGCTCTGCCTCC[G/T]GGGTTCACGCCATTC | 51366 |
rs191135783 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102375524 | GGTGCTATAAGAGTA[G/T]GAGGAATTTCTGAAA | 51366 |
rs191152448 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102399509 | CTCGAACTCCTGACC[G/T]CAGGTGATCAGCCAG | 51366 |
rs191279834 | snp | C/G/T | 6.5895e-05 | 0.00573967 | missense, synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102288213 | TTCTTCCCCGTGTTC[C/G/T]TCCTGTTCATCATGA | 51366 |
rs191289304 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102265766 | TTCTTTCAGTTTATT[A/C]TGTTGAGTTCACTGA | 51366 |
rs191292469 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102328234 | GGGAGGCCAAGGAGG[C/G]AGAATCACTTGGCGC | 51366 |
rs191301733 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102263918 | TTTTGGTAGAGTCAG[A/G]GTCTCGTACGTTGTC | 51366 |
rs191344352 | snp | A/G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102333728 | TGGTTTTATCATTAG[A/G/T]TAGCAGCTCCAACTC | 51366 |
rs191360178 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102282220 | TACATTGGAATTTAC[A/G]AAAATTAAAATTGTA | 51366 |
rs191366189 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102301322 | ATATCTATTTTATAA[C/G]ATTTATGATGTATTT | 51366 |
rs191369781 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102292737 | TGTAACAGTTTTCAA[C/G]AAGTCCTGGATGTAT | 51366 |
rs191370122 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102318555 | CCCAGTCTAGCAAGG[C/T]AGGCCAACGTTCAGA | 51366 |
rs191397791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102391894 | AAAACAGGTAGCAGT[A/G]AAGAAGCCAGCTAAA | 51366 |
rs191534187 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102380246 | TAAAAATACAAATAT[C/T]AGCCACACATGGTGG | 51366 |
rs191539922 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102364654 | CAAATATCAAATTTT[A/T]AAAAACTCTTAAATT | 51366 |
rs191551463 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | UBR5 | GRCh38.p7 | 8:102345854 | GATCACAAGGTCAGG[A/G]TATCAAGACCATCCT | 51366 |
rs191569809 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBR5 | GRCh38.p7 | 8:102394307 | CCTCATCATCTGTCC[A/G]CCTTGGCCTCCCAAA | 51366 |
rs191577495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102314996 | TATATTAATTTTTTC[A/G]TTGTATATTTTTAAG | 51366 |
rs191590093 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | UBR5 | GRCh38.p7 | 8:102347696 | AAGCTGGGGTTGCAG[A/T]AGCACGATCTCGGCT | 51366 |
rs191592838 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102323971 | TCCATCTCAAAAAAA[A/G]GAAAAAGAAAAGAAA | 51366 |
rs191593496 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102302945 | AATTATTTCTGTGAG[C/T]AACACATCACCCACT | 51366 |
rs191602259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102319234 | TCAAAATAAAAGGAT[A/G]GAGTAAGATCTACTA | 51366 |
rs191626873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102284433 | CAAAAATAAAAAGGC[C/T]TTAGTATCAGATTCC | 51366 |
rs191630167 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102371474 | AAAAATTAGTTACAA[G/T]GTTAAATCTGACGCC | 51366 |
rs191639549 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102409594 | TCATTTTATTTGTGA[C/G]TCTCATACATTTCTC | 51366 |
rs191661694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102354607 | CAAATAAATCTGGTG[C/T]TCTTACCCTTAAGCT | 51366 |
rs191663330 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102337074 | CTTAATTTCTTTTCC[A/G]GCTAGGCTGTTATTT | 51366 |
rs191667505 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBR5 | GRCh38.p7 | 8:102252689 | ACACATCTAATACAG[A/C]GTGTTATATAAGTTT | 51366 |
rs191667948 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBR5 | GRCh38.p7 | 8:102402169 | TGCAGTGAGCCAATA[C/T]TGCATCACTGCACTC | 51366 |
rs191670135 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102355633 | CAGAATTTAACTGCT[C/T]ATACTTTGTAAACAT | 51366 |
rs191671587 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102386500 | CTCCTCCATCAAACC[C/G]CATGCAAAAGGGAAG | 51366 |
rs191671925 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | UBR5 | GRCh38.p7 | 8:102356555 | ACGAGGTCAGGAGAT[C/T]GAGACCGTCCTGGCC | 51366 |
rs191676285 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102411875 | CCAGAAACCACCCCC[C/T]CATCTCCGCCGAGTT | 51366 |
rs191844516 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102274937 | CAATATGCAACCTTA[C/G]AGCACAGACTGTAAT | 51366 |
rs191851500 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102307005 | TTCATCCCTACCTGC[A/G]GGATGATGACTCTAC | 51366 |
rs191853258 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102277280 | ATACAGGAATCATAC[A/C/G]CAAGTTTTTTTTCCC | 51366 |
rs191856826 | snp | C/T | 0.00137395 | 0.0261742 | intron-variant | UBR5 | GRCh38.p7 | 8:102314698 | CTAAACACAGCTGTC[C/T]GCATGAGACCTATTT | 51366 |
rs191856991 | snp | A/T | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102260042 | AAAAAAAAAAATATT[A/T]TTTTTTACCCTGGAT | 51366 |
rs191884438 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102339825 | CCATTTACAAGACAT[C/G/T]TGAAATAAGCAAAGA | 51366 |
rs191895066 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102338830 | AATCATTCTGTGCAG[C/G]CTCCTGTGATTTCCC | 51366 |
rs191907612 | snp | C/G | 0.00993945 | 0.0698483 | intron-variant | UBR5 | GRCh38.p7 | 8:102375082 | AAAGTAATTTTTGGC[C/G]GGGCACGGTGGCTCA | 51366 |
rs191932815 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102405346 | TGCTTAAAATTTTCC[A/C]AAATAAAAGGCTTAA | 51366 |
rs191981763 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102310840 | ACAAACACCCTAGTG[C/T]CCCTCTCCAGCCTTT | 51366 |
rs191990725 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102330974 | CCTTCCCCTCCTCAG[A/C]CTATTCAACATGAAG | 51366 |
rs192002282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102345621 | AAGAGCTCTAAAAAT[C/T]CACATACATTTAAAA | 51366 |
rs192106503 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UBR5 | GRCh38.p7 | 8:102336734 | ACGCCAGCACCATAT[A/G]GTTTTGATTGCTTAT | 51366 |
rs192119883 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102361933 | AAGGTAGCATAAAGT[G/T]GGTAGCTGAACCAAT | 51366 |
rs192143697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102291527 | TAAACATAAATCTTA[A/G]AAGGGCAACACCATG | 51366 |
rs192163887 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102258915 | AGGCCTTAAGAACTA[C/G]AAACTCAGAAAATGC | 51366 |
rs192168275 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102369041 | ACATAAATTACCTAC[C/T]TATAAAAAATTTTCC | 51366 |
rs192173966 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102276418 | TCCTTTCTAAAGCCA[A/C]CATTCTGCCTCAGCA | 51366 |
rs192174138 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102293164 | GAGAACTTGAAAGGC[A/C]TACGAAGTTGGAGGC | 51366 |
rs192176329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102255985 | AGCAAATTTTTCTTT[C/T]AGTAGAAGGCAGAAA | 51366 |
rs192181403 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102334755 | ACAAAAGACTTAACC[A/G]GGCATGGTGGCAGGT | 51366 |
rs192192769 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102397014 | CCCGGCCTGGTCTCA[C/T]TTTTAAGTATCTCTG | 51366 |
rs192198169 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | UBR5 | GRCh38.p7 | 8:102356878 | AAATGATAATTTTTT[A/T]AAAAAATCACCATTT | 51366 |
rs192204612 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102407334 | GGGGTTTCACCATGT[C/T]GGCCAGGCTAAGGGG | 51366 |
rs192214430 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102390052 | GCGTGAGCCACCACG[C/T]CCAGCCAAGAAGGAT | 51366 |
rs192238046 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102315479 | TTATATATTAAAGGG[G/T]AGAAATCAGTTTTTA | 51366 |
rs192248564 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102334196 | TCAAAGAAACAGAGT[A/G]ACATACAACTCTACA | 51366 |
rs192252772 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102368005 | AGACACATTTTTAAA[A/T]ATCCATTTTTTAATG | 51366 |
rs192258727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102348480 | CTTATGAGAAAACAA[C/T]TTAGAAAGGGCATGA | 51366 |
rs192361837 | snp | C/T | 8.2392e-05 | 0.00641788 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102266948 | AAAATGTTCCTTACC[C/T]GTACCTTTTCTGAGG | 51366 |
rs192380008 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102354928 | AAGGTCAGGAGTTAA[A/C]GACCAGCCTGGGCAA | 51366 |
rs192387976 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102331782 | TCTCTCCCTAATTCA[A/T]AGGTCACCATTCTCT | 51366 |
rs192445368 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102386201 | CTGGGAGGCCAAGGC[A/G]GGTGGATCACCTGAG | 51366 |
rs192484360 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102383622 | AAATCACAGTAGCTA[G/T]GAAGTTGTCATACAT | 51366 |
rs192490154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102368522 | CAGCCTCAAACTCCT[A/G]GGTTCAAGAGATCCT | 51366 |
rs192503368 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102349606 | GAGAGAGAGCCAAGT[A/G]GAGAGGAGAAGAAAG | 51366 |
rs192517577 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | UBR5 | GRCh38.p7 | 8:102396772 | CTGCAGTGGCGCGAT[C/G]TCGGCTCACTGCAAC | 51366 |
rs192523130 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | UBR5 | GRCh38.p7 | 8:102350054 | CCAGGCATGGTGGAA[C/T]GTGTCAATGGTCTCA | 51366 |
rs192563961 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | UBR5 | GRCh38.p7 | 8:102316526 | TACAGTACAAACGAT[A/T]ATTTTTAAAGATGAG | 51366 |
rs192602469 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102384669 | AAAATAAAACACACA[A/C]ACACAAATTTAGGGA | 51366 |
rs192625236 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102282623 | TGACCCAAGATCACA[C/T]CACTGCACTCCATCC | 51366 |
rs192640545 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102345197 | TGACATCAATTCCAC[A/G]ACGTAAATAGGATCA | 51366 |
rs192644398 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102273766 | TCTCATATTTTCTCT[A/G]GGATATACTACTAAG | 51366 |
rs192644779 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102253305 | GTTTAAAAATGTACA[A/G]CTACATAAATAAAAA | 51366 |
rs192657667 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102273603 | ACACTAGCAAAAAAA[A/T]ACACGAGGCCATTCA | 51366 |
rs192663977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102310476 | CTCAGCCTCCTGAGT[A/G]GCTGGGATTACAGGC | 51366 |
rs192674223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102289661 | AACTCATTTATTACA[C/T]GTGAGACACTTGCTA | 51366 |
rs192683765 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102379437 | ATTAGAATATTATCA[A/G]TAAATAATATTGCCA | 51366 |
rs192740795 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBR5 | GRCh38.p7 | 8:102336814 | CCATTATTGCTTTCA[C/T]TATTTGGGGTATTTT | 51366 |
rs192755920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102371160 | GGTTCTATTTTTTAG[C/T]TTTCTGAGCATCCTC | 51366 |
rs192773301 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102401504 | TCTTCAGTAGCTCTC[A/C]GCTCTCAAAAGTAGC | 51366 |
rs192800698 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102267427 | GAAAGCCAGGTGAAA[G/T]CTGTCAATATTGTAC | 51366 |
rs192819168 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102393667 | AGGCATGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 51366 |
rs192867828 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBR5 | GRCh38.p7 | 8:102330543 | TTCTCCAAGTTAGCA[A/G]TTCTTCCCTTACCTT | 51366 |
rs192876169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102363019 | ACCACACCCGGCTAA[C/T]TTTTGTAATTCAGTA | 51366 |
rs192883298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102264135 | GCCAGGTACTTACGA[C/T]GTTGTGTTTCTTACC | 51366 |
rs192884344 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102288856 | ATTGTACAAAACTAC[G/T]AAATTTTTCTAACAT | 51366 |
rs192894084 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102393312 | ACTCCAATTTTTTTA[C/G]AAGTTGTCTTCTCCC | 51366 |
rs192929995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102326003 | GAGTCCCTGAAAGGG[C/T]TGAGGAGAAGGCAGG | 51366 |
rs192941845 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102359199 | AGTTTTCTGTGATCA[A/G]CCTTCAAACACGTGG | 51366 |
rs192943901 | snp | C/T | 1.65151e-05 | 0.00287355 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102286417 | GCTGATGCTGGGTGT[C/T]GCGGACAGCCCACTG | 51366 |
rs192944019 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102382847 | ACACACACACACACA[C/G]ACACACACACACACA | 51366 |
rs192992707 | snp | A/G | 1.77149e-05 | 0.0029761 | intron-variant | UBR5 | GRCh38.p7 | 8:102285471 | CATAATTGACAGCCA[A/G]AAAAAAATAGTGGAA | 51366 |
rs193028081 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102379825 | AATATGTAGCTATGA[A/C]AGGCAACTGTAAAAA | 51366 |
rs193056413 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102315953 | GTATTTGTACACATC[A/G]AAATTATTTCAAATG | 51366 |
rs193076881 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102276632 | CAACGTATATACAGT[G/T]TATCTTATTTTCAAA | 51366 |
rs193093922 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | UBR5 | GRCh38.p7 | 8:102376836 | AACTTAAAATTTTTT[A/T]AAAAAAATGTCTATG | 51366 |
rs193103327 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102408176 | GGAAACCAGGCAACA[C/T]GTAAAAAGTTAAAAG | 51366 |
rs193138316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102298284 | ATCATTTCCAACCAA[C/T]TGTATCATTTACATA | 51366 |
rs193147214 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102263724 | GAATGCTCTATTTTT[G/T]TTTTGTTTTGTTTTA | 51366 |
rs193170327 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102342146 | GAATGTAACACCACT[C/T]ACTGGAGTAATTATT | 51366 |
rs193175675 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBR5 | GRCh38.p7 | 8:102267799 | AAAAAATACAACTTT[C/T]CATCTAAAATAATAA | 51366 |
rs193179207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102308240 | CATCTTAAACTTCAC[A/G]TCTAAAACCAAACCC | 51366 |
rs193184532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102376368 | AACTTATATTCTGGC[C/T]AAATAAATATTGGTA | 51366 |
rs193233970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102334380 | CACTGCAACCTCCGC[C/T]TCCTGCGTTCCAGCG | 51366 |
rs193236173 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102259423 | AACAAACAGGCTAGT[C/T]ATTAAGAATAGCTTC | 51366 |
rs193248360 | snp | A/T | 0 | 0 | intron-variant | UBR5 | GRCh38.p7 | 8:102390879 | TCAACAAAACGTACA[A/T]ACACGTCAGTGAGAA | 51366 |
rs193294526 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102317643 | ACTGCCTCCTCAAGT[A/G]GGTCCTGACCCCTGA | 51366 |
rs193302453 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102281875 | CATTTCTAAATAGCT[C/G]TTAGGTGAGGTTGAT | 51366 |
rs199499044 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102323844 | GTGGCATGCGCCTGT[A/T]ATCCCAGCTGCTTGG | 51366 |
rs199541021 | snp | A/C | 1.6477e-05 | 0.00287024 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102305124 | TGCTGGTTGGAAAGC[A/C]AACTGATACACAAGC | 51366 |
rs199543891 | snp | C/T | 2.15422e-05 | 0.00328187 | intron-variant | UBR5 | GRCh38.p7 | 8:102286322 | AATTTAAAAAATCTA[C/T]CTAAGTATTCTTAGC | 51366 |
rs199593834 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102319879 | AGAAATAAAGATGTT[A/C]TTTGAAACCAACGAG | 51366 |
rs199599094 | snp | C/G | 5.00338e-05 | 0.00500144 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102293699 | TGCTAGTACTAGCCA[C/G]GGTAAATGGTGCAGT | 51366 |
rs199610150 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102400348 | CCACTCCCTGAGCTC[A/G]CTAATCTATAACCTC | 51366 |
rs199617001 | snp | A/C/T | 0.000165325 | 0.00909068 | intron-variant | UBR5 | GRCh38.p7 | 8:102295590 | TACTCAGCTGTGCTG[A/C/T]GCTCTTTTGATTTAA | 51366 |
rs199617599 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102354491 | AGCTTATACCTATCA[C/T]CTATTGTTCAACGGT | 51366 |
rs199631328 | snp | C/T | 1.65315e-05 | 0.00287498 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102272759 | TGAATGAGAAGATCT[C/T]GATCCCGATCAACCT | 51366 |
rs199656183 | in-del | -/AAAG | 0.00716266 | 0.059414 | intron-variant | UBR5 | GRCh38.p7 | 8:102308943 | TTTTAAAAAAAAAAA[-/AAAG]AAAGAAAGAAAGAAA | 51366 |
rs199660897 | in-del | -/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102368437 | TTTCTTTTTTTTTTT[-/C]CCAAGGGGCACAGTC | 51366 |
rs199669966 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102320989 | CAATATCATACTGAA[C/T]GGGCAAAAACTGGAA | 51366 |
rs199681698 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102323896 | TTAAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 51366 |
rs199683171 | snp | A/G | 3.41799e-05 | 0.00413385 | intron-variant | UBR5 | GRCh38.p7 | 8:102327701 | TCTTTCTATACATAC[A/G]CAAGCATTCACCGAT | 51366 |
rs199686475 | snp | C/T | 0.0648353 | 0.16797 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102288240 | ATGATGATCCTCTTC[C/T]CCAGCCACACCCTCC | 51366 |
rs199706370 | snp | C/T | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102305218 | CTGCTCTAAAACAAC[C/T]GCTTGCTCAAGATTC | 51366 |
rs199731103 | snp | A/G/T | 0.0171276 | 0.090942 | intron-variant | UBR5 | GRCh38.p7 | 8:102396713 | ATATATATATATATT[A/G/T]TTTTTTTTCTTGAGA | 51366 |
rs199733003 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102319112 | AAATGTAAATGGACT[A/C]AATGCTCCAATTAAA | 51366 |
rs199734663 | in-del | -/A | | | utr-variant-3-prime, downstream-variant-500B | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102252324 | TTTTATGATTTACTT[-/A]AAAAAAAAATCTTTT | 51366 |
rs199735996 | in-del | -/A | 0.0185938 | 0.0946107 | intron-variant | UBR5 | GRCh38.p7 | 8:102273998 | TTACAAAATAAAACC[-/A]AAAGAGGAAAAACGA | 51366 |
rs199777560 | in-del | -/TA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102290911 | TTTTTTTTTTTTTTT[-/TA]AATTTTGGAGTATCT | 51366 |
rs199818770 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102361393 | CTGTATGCCAGATTT[-/A]AAAAAAAAAAAGCAT | 51366 |
rs199834871 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102315901 | TGAAAAACTTCATCA[A/G]TTACAGGCTTTAAAT | 51366 |
rs199835844 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102275511 | TATAAGAAAATCTAA[A/G]TACCTTTACCTCTAG | 51366 |
rs199878072 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102255418 | TTCTATATAAAGGGA[A/C]AGAAAAAAAAAAAAA | 51366 |
rs199882303 | in-del | -/G | 0.0103295 | 0.0711199 | intron-variant | UBR5 | GRCh38.p7 | 8:102328121 | CAAATGAATGTCTAA[-/G]GCCATCTTTAAGGTC | 51366 |
rs199891687 | snp | A/T | 1.65979e-05 | 0.00288074 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102323443 | GGAATCCCAGCACTA[A/T]TTGAAAATGCAACTG | 51366 |
rs199900374 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102322294 | GGATATGAACAGACA[A/C]TTCTCAAAAGAAGAC | 51366 |
rs199903814 | snp | C/G | 0.00199802 | 0.0315439 | intron-variant | UBR5 | GRCh38.p7 | 8:102269137 | ACAAATGTTACTTGA[C/G]TACTCTCTAAAACCT | 51366 |
rs199906802 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102318264 | CTGATGGAGCTGAAA[A/G]CCAAGGCTCGAGAAC | 51366 |
rs199919155 | snp | C/G | 1.64879e-05 | 0.00287118 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102281464 | ACAGAGCATAATTTA[C/G]GAAGTCTCCTCGTGC | 51366 |
rs199928719 | snp | C/T | 0.000430079 | 0.0146579 | intron-variant | UBR5 | GRCh38.p7 | 8:102360044 | AGACCATCTGTAAGA[C/T]GGTGCCTTCAACTGG | 51366 |
rs199936094 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102304963 | ACCTTCTGAGAAAGT[-/A]AAAAAAAAAAAAAAA | 51366 |
rs199953650 | snp | C/T | 6.09094e-05 | 0.00551824 | intron-variant | UBR5 | GRCh38.p7 | 8:102294141 | TTATATTCACTCTAT[C/T]AATGTTAAGATACTT | 51366 |
rs199977699 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102392623 | AAAAAAAAAAAAAAA[A/C]AAAAAACAAAAAACA | 51366 |
rs200002154 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102268450 | CTCAGGCAATCTGCC[C/T]GCCTCAGCCTCCCAA | 51366 |
rs200003326 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102390415 | ATCCCAGCTACTCGG[A/G]AGGCCGAGCTGAGAT | 51366 |
rs200050927 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102407283 | TACAGGCGTCCACCA[C/T]CACACCCAGCTAATT | 51366 |
rs200052233 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102321210 | TCTCAGCCCAAAATC[A/T]CCTTAAGCTGATAAG | 51366 |
rs200053483 | snp | C/G | 0.000419326 | 0.0144737 | intron-variant | UBR5 | GRCh38.p7 | 8:102299436 | GACTAGGCAGACAAA[C/G]AGTACAGATTCTTAC | 51366 |
rs200058935 | in-del | -/TGTT | 0.0205511 | 0.0992634 | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102252924 | AATATGTAAAGTGAC[-/TGTT]TGTTTTAAGTCACTT | 51366 |
rs200072772 | snp | C/T | | | intron-variant, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102258979 | CATTTTTTTTAAATG[C/T]CCTACCTGATTCATC | 51366 |
rs200157694 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102318523 | ACACTCTTCAGGATA[A/T]TATCCAGGAGAACTT | 51366 |
rs200161535 | in-del | -/AAAAT | 0.0804634 | 0.183732 | intron-variant | UBR5 | GRCh38.p7 | 8:102298359 | ATCTATCCAAACTGA[-/AAAAT]ATGTAACTCATTTAG | 51366 |
rs200163411 | snp | C/T | 0.000918454 | 0.0214099 | intron-variant | UBR5 | GRCh38.p7 | 8:102327913 | TAAAGAATAAAATAT[C/T]AGAACTTTAAATAAA | 51366 |
rs200180305 | in-del | -/A | 0.0142736 | 0.0832652 | intron-variant | UBR5 | GRCh38.p7 | 8:102357569 | ATCCTATCTCTATTT[-/A]AAAAAAAAAGCAGCA | 51366 |
rs200182279 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102404729 | CCTGACCAACATGGT[C/G]AAACCCCGTCTCCAC | 51366 |
rs200190753 | in-del | -/TG | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102306598 | AATTTATACAAAATA[-/TG]TGTTGAGAGAAAATG | 51366 |
rs200205378 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102320990 | AATATCATACTGAAT[A/G]GGCAAAAACTGGAAG | 51366 |
rs200208507 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102335152 | CTAAGAGAAATAAGA[C/T]AGACACAGGGAAAAA | 51366 |
rs200210771 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102321030 | TGAAAACTGGCACAA[A/G]ACAGGGATGTCCTCT | 51366 |
rs200231266 | snp | A/G | 0.00199808 | 0.0315444 | intron-variant | UBR5 | GRCh38.p7 | 8:102280384 | ATTAGCAGATTTTCT[A/G]TGCACTAACTTTGAT | 51366 |
rs200249122 | snp | C/T | 1.65015e-05 | 0.00287237 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102262011 | CTGAGACGCGAGGAT[C/T]AGTTGCCGCAAACTC | 51366 |
rs200256575 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102318671 | AATGAAGGAAAAAAT[G/T]TTAAGGGCAGCCAGA | 51366 |
rs200259932 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102274658 | AGTCACCTGAACCCA[A/G]GAGGCGGAGGTTGCA | 51366 |
rs200281113 | in-del | -/TTC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102351601 | TAGAAAGCTGTTTCA[-/TTC]CAACAACAGTGTGGA | 51366 |
rs200283351 | in-del | -/GGGGGT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102283352 | AAGGCGGGGGGGGGG[-/GGGGGT]GAGTAGGGGAAAATG | 51366 |
rs200298404 | snp | C/T | 6.87959e-05 | 0.00586457 | intron-variant | UBR5 | GRCh38.p7 | 8:102293558 | AAGTCAAACACGACA[C/T]TTCCAGAGAAGGATT | 51366 |
rs200305762 | snp | C/T | 0.000582032 | 0.0170493 | intron-variant | UBR5 | GRCh38.p7 | 8:102327692 | CTCAAAGCATCTTTC[C/T]ATACATACACAAGCA | 51366 |
rs200309871 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102318994 | AAAATCATGCCAAAA[A/T]GTAAAGACCATCGAG | 51366 |
rs200315433 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102288207 | AGCATTTTCTTCCCC[A/G]TGTTCTTCCTGTTCA | 51366 |
rs200341816 | in-del | -/AC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102395402 | TCTATTTATATATAT[-/AC]ACACACACACACGTA | 51366 |
rs200344688 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102323694 | TTTCTAGGCCAGGCG[C/T]GGTGGCTCACGCCTG | 51366 |
rs200345849 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102269983 | ACACCATCTTTAATT[A/C]AAAAGCAAAAAAATA | 51366 |
rs200347753 | snp | A/C | 0.001998 | 0.0315437 | intron-variant | UBR5 | GRCh38.p7 | 8:102329232 | AAAAATTACTATTTT[A/C]TATGTTGATATGTAG | 51366 |
rs200399762 | snp | C/T | 0.000349124 | 0.0132076 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102257670 | TCATCTTCTCTACTA[C/T]TGACCAGAACCAACG | 51366 |
rs200402536 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102386706 | ATATAGGCCGGGCGC[A/G]GTGGCTCATGCCTGT | 51366 |
rs200415270 | snp | C/T | 1.65411e-05 | 0.00287581 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102298932 | TGAGCATTCGCCTTT[C/T]GATCCTTGGATTCTA | 51366 |
rs200442116 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102294104 | TAGTGTACCTAGTAG[A/G]GTATCTAAAAGCTTT | 51366 |
rs200446456 | snp | A/C/G | 0.000839014 | 0.0204679 | missense, synonymous-codon, nc-transcript-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102412187 | CCTGTCATTGAGCTG[A/C/G]TCCTCGGTGCCCGGC | 51366 |
rs200478816 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102296254 | ACCAGAATTCTTTTA[A/T]TATCTATTAAAATTT | 51366 |
rs200500892 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102321060 | TCTCACCACTCCCAT[A/T]CAACATAGTGTTGGA | 51366 |
rs200522889 | in-del | -/GAAA | 0.0170251 | 0.090679 | intron-variant | UBR5 | GRCh38.p7 | 8:102309006 | CCCTTAAGGATATAG[-/GAAA]GAAAGTTATTTTTTA | 51366 |
rs200547907 | in-del | -/AATT | 0.0479149 | 0.147179 | intron-variant | UBR5 | GRCh38.p7 | 8:102323096 | AGTATAATAATAATA[-/AATT]AATTAATTAATTAAT | 51366 |
rs200551670 | snp | A/T | | | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102414538 | ACAGATCTAAAAAAA[A/T]TTTTTTTTTTTTGAG | 51366 |
rs200599625 | snp | C/T | 0.000148337 | 0.00861085 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102327808 | TGTAAAGAAACTATC[C/T]GCTCTCCTTGAAGTT | 51366 |
rs200605383 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102322437 | TTAAAAAGTCAGGAA[A/T]CAACAGGTGCTGGAG | 51366 |
rs200607455 | snp | A/T | 1.64798e-05 | 0.00287047 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311798 | AGCAATGCTGCTTGT[A/T]GGAAAATTATTTTCC | 51366 |
rs200615403 | in-del | -/ACAGAGGC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102355780 | GTTCTGGCAGAGAGA[-/ACAGAGGC]ACAAAGAGGGGTTTA | 51366 |
rs200652945 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102298507 | AAAATAAGAAAAATT[A/T]TATGTAAAAATATTA | 51366 |
rs200655579 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102323854 | CCTGTTATCCCAGCT[A/G]CTTGGGAGGCTGAGG | 51366 |
rs200675333 | snp | A/G | 0.00199792 | 0.0315431 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102305239 | CTCAAGATTCATTAG[A/G]TATTGTCGACAGGCC | 51366 |
rs200685740 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102324407 | AATAACTTACAGAGA[A/G]AAAAAAAAAAAAAAC | 51366 |
rs200690228 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102255420 | CTATATAAAGGGACA[A/G]AAAAAAAAAAAAAAA | 51366 |
rs200697827 | in-del | -/AGG | 0.0209421 | 0.100162 | intron-variant | UBR5 | GRCh38.p7 | 8:102291778 | TGCCATCTACTATTC[-/AGG]AGAATACAAAAAAAA | 51366 |
rs200700932 | snp | C/T | 0.00104416 | 0.0228252 | intron-variant | UBR5 | GRCh38.p7 | 8:102270021 | CAGTTAAGAGGTAAC[C/T]AAGTACACAGTACAC | 51366 |
rs200708779 | in-del | -/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102343860 | CGTCTCAAAAAAAAA[-/G]AGGGGGGGGTGGGCA | 51366 |
rs200726893 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102269989 | TCTTTAATTCAAAAG[G/T]AAAAAAATAACACAG | 51366 |
rs200736482 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102386222 | ATCACCTGAGGTCAG[G/T]AGCTTGAGACCAGCC | 51366 |
rs200773517 | snp | A/C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102318563 | AGCAAGGCAGGCCAA[A/C/T]GTTCAGATTCAGGAA | 51366 |
rs200777265 | snp | C/T | 0.000197759 | 0.00994184 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102288261 | CACACCCTCCACCAC[C/T]TCAACCTAAATCCAG | 51366 |
rs200802228 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102399696 | TCACACCTGTAATCC[C/G]AACACTTTGGGAGGC | 51366 |
rs200802377 | snp | A/T | 9.90344e-05 | 0.00703615 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102281311 | GTTCTAGTTGAGGTG[A/T]ATCCAATGTTGTCTG | 51366 |
rs200808254 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102319784 | CTCAGGATTAAGAAA[A/C]TCACTCAAAACTGCT | 51366 |
rs200835124 | in-del | -/G | 0.0547245 | 0.156101 | intron-variant | UBR5 | GRCh38.p7 | 8:102409636 | AGTCAAGCTACAGTA[-/G]CAGTAGCTTTTTTAT | 51366 |
rs200838820 | in-del | -/T | 0.160609 | 0.233472 | intron-variant | UBR5 | GRCh38.p7 | 8:102277693 | CCTTACCCACCCCCC[-/T]CCTTTAAATTCACTT | 51366 |
rs200854784 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102317793 | TCACGAAAATCTGCT[A/C]TTCTGCAGCCAGCAC | 51366 |
rs200857170 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102319885 | AAAGATGTTATTTGA[A/T]ACCAACGAGAACAAA | 51366 |
rs200872308 | snp | A/G | 3.34622e-05 | 0.00409023 | intron-variant | UBR5 | GRCh38.p7 | 8:102272813 | AAAGTAGTAAATTCA[A/G]TGTTGGAAAGTAGCT | 51366 |
rs200880178 | snp | C/G | 0.00199792 | 0.0315431 | intron-variant | UBR5 | GRCh38.p7 | 8:102295131 | AGGAGAAACGAAAGA[C/G]AGAATGAACTGTAAA | 51366 |
rs200903782 | snp | A/G | | | intron-variant, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102258978 | ACATTTTTTTTAAAT[A/G]TCCTACCTGATTCAT | 51366 |
rs200927604 | snp | C/T | 3.29527e-05 | 0.00405898 | missense, nc-transcript-variant, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102277111 | GCAGCACGGGCTGTT[C/T]TTCCCCTTCTTTTTT | 51366 |
rs200928933 | snp | C/T | 1.64863e-05 | 0.00287104 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102326572 | CAGTGATGTTCGGCA[C/T]TGAAGAAATACCAGC | 51366 |
rs200952254 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102396711 | CATATATATATATAT[-/A]TTTTTTTTTTCTTGA | 51366 |
rs200960876 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102356276 | CCAACATGGTGAAAC[C/T]CTGTCTCTACTAAAA | 51366 |
rs200997298 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | UBR5 | GRCh38.p7 | 8:102321538 | TTATAGATTCAATGG[C/T]ATCCCCATCAAGCTA | 51366 |
rs201051086 | in-del | -/A | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102278516 | GTAAAAGTTGTAGCC[-/A]AAATTACACATGCTC | 51366 |
rs201051796 | snp | A/C | 5.27969e-05 | 0.00513767 | intron-variant | UBR5 | GRCh38.p7 | 8:102265052 | TTAGAAAATCTCATA[A/C]ATTGAAATGTTTTAA | 51366 |
rs201084269 | in-del | -/A | 0.0189856 | 0.0955633 | intron-variant | UBR5 | GRCh38.p7 | 8:102260040 | TAAAAAAAAAAATAT[-/A]TTTTTTTTACCCTGG | 51366 |
rs201087348 | in-del | -/C | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102317465 | TGGAGCCCACCACAG[-/C]TCAAGGAGGCCAGCC | 51366 |
rs201088734 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102318731 | GCCCATCAGACTAAC[A/T]GCTGATCTCTCGGCA | 51366 |
rs201098712 | in-del | -/T | 0.0399052 | 0.1355 | intron-variant | UBR5 | GRCh38.p7 | 8:102268374 | CCAGCCACTTTTAAC[-/T]TTTTTTTTTAGTAGA | 51366 |
rs201163706 | in-del | -/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102351428 | ACACACACACACACA[-/C]AAAAAAACCTCAGTG | 51366 |
rs201214883 | snp | C/T | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102305193 | TGAATGTCTGCAGCA[C/T]CTGTAGATTCTGCTC | 51366 |
rs201215529 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102322346 | ATGAAAAAATGCTCA[A/T]CATCACTGGCCATCA | 51366 |
rs201231459 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102281829 | TAATCCCCAGAGTTT[C/T]AGTAGGTCTGGGGTA | 51366 |
rs201236904 | snp | C/T | 1.6643e-05 | 0.00288465 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102299498 | AGTACCGGTTGCTGC[C/T]GTGGTAAGAGATCCC | 51366 |
rs201256532 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102399717 | TTTGGGAGGCCAAAG[C/G]GGGTGGATCACGAGG | 51366 |
rs201269346 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102322663 | TACTGCGGCACTATT[C/G]ACAATAGCAAAGACT | 51366 |
rs201317222 | snp | C/T | 0.00199802 | 0.0315439 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102280399 | GTGCACTAACTTTGA[C/T]TGGTGTCATCATCAT | 51366 |
rs201325772 | snp | A/G | 0.000132444 | 0.0081366 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102259001 | TGATTCATCATTGAA[A/G]GAGGTAAAACTGATC | 51366 |
rs201328061 | snp | C/T | 1.64806e-05 | 0.00287054 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102327790 | GTGTAAAGGGCACAG[C/T]AATGTAAAGAAACTA | 51366 |
rs201330026 | snp | G/T | 3.35149e-05 | 0.00409345 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102299539 | CCAGGATAAAATCAA[G/T]GTCACCATCTTTCAG | 51366 |
rs201333453 | snp | A/C/T | 0.00089081 | 0.0210874 | intron-variant | UBR5 | GRCh38.p7 | 8:102295536 | AGGTGCTCTCCCCTG[A/C/T]AAAACAGAATGTTGT | 51366 |
rs201341194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102346884 | TTGTCTGACATTAAG[C/T]GTTCTACGAGATCCA | 51366 |
rs201346852 | in-del | -/AAAG | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102365485 | AAAAAAAAAAAACAC[-/AAAG]AAAATAACCTCATAA | 51366 |
rs201347790 | snp | C/T | 0.00299548 | 0.0385846 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102271245 | AATCTCTGCATTAAA[C/T]CTAGAAGAAAATCAG | 51366 |
rs201360534 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102312951 | GTTATTTGATTTTAA[A/C]AAATTTAAACAGCCA | 51366 |
rs201370980 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102319048 | AACGAGCAAAATAAC[C/G]AGCTAACATCATGAC | 51366 |
rs201399139 | in-del | -/AC/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102361979 | AATTGTTTAAAAAAA[-/AC/C]CAAAACAAAACAAAA | 51366 |
rs201400150 | in-del | -/G | 0.0570711 | 0.158992 | intron-variant | UBR5 | GRCh38.p7 | 8:102396713 | TATATATATATATTT[-/G]TTTTTTTTCTTGAGA | 51366 |
rs201427220 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102310526 | TAATTTTTGTATTTT[C/T]AGTAGAGATAGGGTT | 51366 |
rs201430960 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102278162 | GATAATAAAAAATAT[C/T]CTATTCAACTACATG | 51366 |
rs201464176 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102321090 | AAGTTCTGGCCAGGG[C/G]AATTAGGCAGGAGAA | 51366 |
rs201476219 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102323711 | GTGGCTCACGCCTGT[A/T]ATCCCAGCACTTTGG | 51366 |
rs201489668 | snp | C/T | 0.00764454 | 0.0613501 | intron-variant | UBR5 | GRCh38.p7 | 8:102314874 | ATAAGAAATAAGATT[C/T]TCCTTATAATTAGAT | 51366 |
rs201491273 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102354031 | GCCAGATCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 51366 |
rs201511543 | in-del | -/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102335262 | AGTGGTTACCATGGG[-/C]TGACAAGCAGTGTGG | 51366 |
rs201545046 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102318697 | CCAGAGAGAAAGGTC[A/G]GGTTACCCACAAAGG | 51366 |
rs201547772 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102323883 | GGCAGAGAATTGCTT[A/G]AACCTGGGAGGCGGA | 51366 |
rs201600408 | snp | A/G | 0.00199806 | 0.0315443 | intron-variant | UBR5 | GRCh38.p7 | 8:102293948 | AAAATCAAAAAGGAT[A/G]CCTTACTTTTTCTTT | 51366 |
rs201620219 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102269184 | TACAATCTTTTATTT[-/A]AAAAAAAAATAAAAT | 51366 |
rs201635392 | snp | G/T | 0.048855 | 0.148461 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295429 | CTTCAGGACTGGCTG[G/T]TTTTCGGTTACGATC | 51366 |
rs201649930 | in-del | -/TTGT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102371578 | ATGCCTGATTCTGGG[-/TTGT]TTGTTTTTTTTTTTT | 51366 |
rs201650970 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102408261 | TCCCATCTACTGTCT[C/G]AACTGTTCCTCCCTG | 51366 |
rs201722625 | in-del | -/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102277686 | AACCAGCCTTACCCA[-/C]CCCCCCTCCTTTAAA | 51366 |
rs201723272 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102396665 | ACACACACACACACA[C/T]ATATATATATATATA | 51366 |
rs201733014 | snp | A/G | 0.000214226 | 0.0103473 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102277132 | CTTCTTTTTTTTGCC[A/G]GTTTTGCATGTTCAT | 51366 |
rs201752299 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102347645 | GATCCTTAAAAAAAC[-/T]TTTTTTTTTTGAGAC | 51366 |
rs201756791 | snp | C/T | 0.00199792 | 0.0315431 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285708 | AGCAGCTGCTGCAGC[C/T]GCAGCACTTGTACTG | 51366 |
rs201762221 | snp | C/G | 0.00199798 | 0.0315436 | intron-variant | UBR5 | GRCh38.p7 | 8:102305071 | AAAGACCTTGCTATA[C/G]TTCTTAATCTCACCC | 51366 |
rs201766433 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102396639 | ATATATATATACACA[C/T]ATATATATATACACA | 51366 |
rs201768890 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102394624 | GATCTGCAGTTTTTT[A/G]CCAATAACAGTGAGG | 51366 |
rs201774012 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102318564 | GCAAGGCAGGCCAAC[A/G]TTCAGATTCAGGAAA | 51366 |
rs201793668 | in-del | -/TGTG | 0.0103295 | 0.0711199 | intron-variant | UBR5 | GRCh38.p7 | 8:102354120 | TCTGAATGATGTGAC[-/TGTG]TGTATGTGTATATTT | 51366 |
rs201815811 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102335202 | TTATATGTGAAGTCT[A/G]TTTTTTTTTTTAAAG | 51366 |
rs201820159 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102317998 | ATGGGGAAAAACAGA[A/G]CAGAAAAACTGGAAA | 51366 |
rs201832826 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102329735 | GACACTATGTACAGA[A/C]CCACCACTCTCACAT | 51366 |
rs201838360 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102321002 | AATGGGCAAAAACTG[G/T]AAGCATTCCCTTTGA | 51366 |
rs201840796 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102318457 | AAAGACCAAATCTAC[A/G]TCTGATTGGTGTACC | 51366 |
rs201846930 | snp | A/T | 0.00330589 | 0.0405218 | intron-variant | UBR5 | GRCh38.p7 | 8:102264453 | ATTGTGAATACAATT[A/T]GGTTCATCAAAATCA | 51366 |
rs201847877 | snp | A/G | 0.000170146 | 0.00922194 | intron-variant | UBR5 | GRCh38.p7 | 8:102298387 | TAGGATCTGAAATAA[A/G]TTACCTTTTGCAATT | 51366 |
rs201850123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102290734 | GAGGTGGGAGGATTG[C/T]TTGAGGACAGGAATT | 51366 |
rs201850347 | snp | A/G | 1.96798e-05 | 0.0031368 | intron-variant | UBR5 | GRCh38.p7 | 8:102257733 | CTAAGAATGAAGAAT[A/G]TAAATAAAATATACT | 51366 |
rs201851148 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102318515 | GTTGGAAAACACTCT[G/T]CAGGATAATATCCAG | 51366 |
rs201871216 | in-del | -/T | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102318694 | AGCCAGAGAGAAAGG[-/T]TCAGGTTACCCACAA | 51366 |
rs201900632 | snp | A/T | 1.66788e-05 | 0.00288775 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102265105 | GTTCTTTTACCTGCC[A/T]ATGTTTCTGAAACAA | 51366 |
rs201911188 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102274752 | AAAAAAAAAAAGAAA[C/T]AAATCTAAGAAGCAA | 51366 |
rs201928010 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102389764 | TATTAATATTAAGGA[-/T]TTTTTTTTTTTTTTG | 51366 |
rs201951911 | snp | C/T | 1.67332e-05 | 0.00289246 | intron-variant | UBR5 | GRCh38.p7 | 8:102346221 | ATGAGAAAAACATGA[C/T]GGTGATCCACCAACC | 51366 |
rs201952201 | in-del | -/G | 0.0209421 | 0.100162 | intron-variant | UBR5 | GRCh38.p7 | 8:102361726 | TAATTTCCAATAGTA[-/G]TACACAAAACAACTG | 51366 |
rs201963097 | snp | A/G | 0.00199808 | 0.0315444 | intron-variant | UBR5 | GRCh38.p7 | 8:102361219 | TGGCTGAGAGATAAA[A/G]AAAGAAAAAGTTAAA | 51366 |
rs202000266 | in-del | -/TAG | 0.00953873 | 0.0683987 | intron-variant | UBR5 | GRCh38.p7 | 8:102265478 | AAGCTTGTGTATTAT[-/TAG]GTCTTTAACGTCTCT | 51366 |
rs202019786 | snp | A/G | 6.59805e-05 | 0.00574333 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102326559 | ACCTGGGTACCAACA[A/G]TGATGTTCGGCATTG | 51366 |
rs202039862 | snp | A/C/T | 4.99566e-05 | 0.00499762 | intron-variant | UBR5 | GRCh38.p7 | 8:102312290 | AAACTCCATAATAAA[A/C/T]TCACGGAGTCAGTTC | 51366 |
rs202074198 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102385087 | GCTGTTTCTTCCATC[A/G]CCATTTCTGACTGAA | 51366 |
rs202081267 | snp | C/T | 0.00199806 | 0.0315443 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102323440 | TTAGGAATCCCAGCA[C/T]TAATTGAAAATGCAA | 51366 |
rs202102523 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102322426 | AACAGCGATCATTAA[A/G]AAGTCAGGAAACAAC | 51366 |
rs202108259 | snp | C/T | 1.69712e-05 | 0.00291295 | intron-variant | UBR5 | GRCh38.p7 | 8:102293587 | TTAATCAGAATCTGT[C/T]ACCTGGTAGCAATTT | 51366 |
rs202109925 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102321774 | GAACAGAGCCCTCAG[A/G]AATAATGCCACATAT | 51366 |
rs202111651 | snp | C/T | | | splice-donor-variant, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102258984 | TTTTTAAATGTCCTA[C/T]CTGATTCATCATTGA | 51366 |
rs202127617 | snp | C/T | 9.88875e-05 | 0.00703093 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102360173 | CTCCCTGCCCCCGAG[C/T]TGCTGTTCAACTTTG | 51366 |
rs202190508 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102284275 | ATGTGATTTGAGAAA[C/T]AAAGAGCAGCACTGG | 51366 |
rs202193392 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102367919 | CAACCCGTTAGAAAT[C/G]AGTCTCTTCATCTGT | 51366 |
rs202215133 | in-del | -/ATATCATAG | 0.0146672 | 0.084371 | intron-variant | UBR5 | GRCh38.p7 | 8:102394527 | TCTTTACCACAGTTA[-/ATATCATAG]ACTTTTTCACCTCTT | 51366 |
rs202221615 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102275454 | AGCTATTGTTATTTT[A/G]CATGTTTTAAAATTT | 51366 |
rs267601686 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102342672 | GAGTCTCTCTCTAAG[A/G]GAAGAAGGAGAACTG | 51366 |
rs367545220 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102351768 | TTTTCAAGTTATATA[G/T]TAAAACAATTATGCA | 51366 |
rs367552264 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102376061 | CAGACTGGTCCTACC[A/G]AGTCAATCAAAAGCC | 51366 |
rs367564954 | snp | G/T | | | intron-variant, utr-variant-5-prime | UBR5 | GRCh38.p7 | 8:102302305 | GGACAATACTGAGGA[G/T]ATACCACCTTGGCTG | 51366 |
rs367568465 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102361420 | GCATGAATGCAATCT[A/G]TAATTCAAATAAGCC | 51366 |
rs367580435 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBR5 | GRCh38.p7 | 8:102389262 | CTAAGGCTAGGTCAC[A/G]AAAAGGAATTCCAGC | 51366 |
rs367586487 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102284533 | AATGCAAGCAAGTCA[C/T]TTCTTTCTCCCTTCA | 51366 |
rs367589403 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102256240 | CCCGGGAGGTGGAGC[C/T]TGCAGTGAGCCGAGA | 51366 |
rs367597527 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102272848 | TTTTTCTATGTACAA[C/T]CTGAAAATCTAGTTT | 51366 |
rs367602569 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102316251 | TTATAATCATAACAT[A/C]TGAGTATAAATGGAA | 51366 |
rs367649268 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102353371 | TGACTCAAAATGAAC[C/T]AAGGATATCATACCT | 51366 |
rs367661393 | snp | C/T | 1.66084e-05 | 0.00288165 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102294083 | TTTGTTTTGGAGTTC[C/T]TTCACTAGTGTACCT | 51366 |
rs367664345 | snp | C/T | 5.56086e-05 | 0.00527268 | intron-variant, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102258948 | ACTGACCTATCTATA[C/T]AGTTCATTCTTTAAA | 51366 |
rs367672960 | snp | A/G/T | 0.000214134 | 0.0103453 | missense, synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311413 | TGGAAGATCCAGCCA[A/G/T]TCGGGATCCCTTATT | 51366 |
rs367676797 | snp | A/G | 0.000133905 | 0.00818134 | intron-variant | UBR5 | GRCh38.p7 | 8:102275842 | GCCTGTAAGAAGTTT[A/G]AGGGAAGGGGTGGGG | 51366 |
rs367685791 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102337320 | CTATGCTGAATGGAA[C/T]TGGCAAGAGTAGGCA | 51366 |
rs367689675 | snp | C/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102327774 | TTCCAGCTGAGCGCA[C/G]GTGTAAAGGGCACAG | 51366 |
rs367703903 | snp | A/G | 1.6477e-05 | 0.00287024 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102286524 | AAGGTCTCCTGTTCT[A/G]TGTCGTCACTCTGAC | 51366 |
rs367727160 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102318567 | AGGCAGGCCAACGTT[A/C]AGATTCAGGAAATAC | 51366 |
rs367743863 | snp | A/T | 0.000205023 | 0.0101227 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102412245 | GTCATGGTGCTTTCC[A/T]TCTCGTCCTCCACTC | 51366 |
rs367790396 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102407636 | GACATAGTGGTATGC[A/G]TCTGTAACTTGGGAG | 51366 |
rs367798387 | snp | A/T | 0.000198321 | 0.00995596 | intron-variant | UBR5 | GRCh38.p7 | 8:102329221 | AAAGCATAAAAAAAA[A/T]TTACTATTTTATATG | 51366 |
rs367849599 | in-del | -/CA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102266851 | TTTTATTTATAAAGA[-/CA]GTTTCTTCAGAAATC | 51366 |
rs367880522 | snp | A/C | 0.000307953 | 0.0124049 | intron-variant | UBR5 | GRCh38.p7 | 8:102360043 | CAGACCATCTGTAAG[A/C]TGGTGCCTTCAACTG | 51366 |
rs367884677 | snp | A/C | 1.66799e-05 | 0.00288785 | intron-variant | UBR5 | GRCh38.p7 | 8:102297431 | ACAAAGATATGATTA[A/C]TACAGGAAAATGTAG | 51366 |
rs367920662 | snp | C/T | | | intron-variant, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102258494 | TCAAGAGGACTTTCA[C/T]TACCACTCCTTATTC | 51366 |
rs367940261 | snp | C/T | 0.000549748 | 0.0165702 | intron-variant | UBR5 | GRCh38.p7 | 8:102312508 | TATAGGCAAATTCAA[C/T]GAACATTAGCAATAG | 51366 |
rs367940786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102394165 | TCCCGGGTTCAAGCC[A/G]TTCTCCTGCCTCAGC | 51366 |
rs367958134 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102274702 | ATGCCACTATGCTCT[C/G]GCCAGGGCGACAAAG | 51366 |
rs367962786 | in-del | -/A | 0.011197 | 0.0739806 | intron-variant | UBR5 | GRCh38.p7 | 8:102275623 | TTCAGTTAGGATCTT[-/A]AAAAAAAAAAAATGC | 51366 |
rs367975491 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102382152 | CTATCCTTGCCATCA[G/T]GCCACACCTGCCACG | 51366 |
rs367989462 | snp | C/G | 9.91391e-05 | 0.00703987 | intron-variant | UBR5 | GRCh38.p7 | 8:102360056 | AGATGGTGCCTTCAA[C/G]TGGCCACAACTTACC | 51366 |
rs368014945 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102308587 | GCCAATCATATAGAA[A/G]TACAGTACATACAAT | 51366 |
rs368015264 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102279285 | GTAACAGACCTTTAA[C/T]CTGCTCAATCCAAAA | 51366 |
rs368029393 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102334118 | TGGTTCCAACAGGGA[A/G]GTTGCTCCAAAGAGC | 51366 |
rs368035752 | in-del | -/ATACATGTATACAATGTGT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102370500 | ATGTACACAATGTGT[-/ATACATGTATACAATGTGT]TAATAATCAAATCAG | 51366 |
rs368040542 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102407516 | ATGCCTGTAATCCCA[A/G]CATTTTGGTAGGCTG | 51366 |
rs368049967 | snp | C/T | 1.92443e-05 | 0.0031019 | utr-variant-3-prime, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102254287 | TATTACACAGCAATA[C/T]ACACTTTTTATACTC | 51366 |
rs368052233 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102317059 | GGGTTCATCTCACTA[A/G]GGAGTGCCAGACAGT | 51366 |
rs368055855 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102343048 | ATACACTCCTCGTTT[C/G]TCTACTGGTGGGTTT | 51366 |
rs368060261 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102399741 | CACGAGGTCAGGAGT[A/T]CGAGACCAGCCTGGC | 51366 |
rs368060537 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102264667 | TACAGCCTCCTTTCT[A/G]TTCAGCATAAAGTAC | 51366 |
rs368062302 | snp | C/T | 0.000455437 | 0.0150839 | intron-variant | UBR5 | GRCh38.p7 | 8:102286319 | CATAATTTAAAAAAT[C/T]TATCTAAGTATTCTT | 51366 |
rs368075628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102259688 | TGATTTCAACTCTAA[C/T]AGTATGACTCCAAAG | 51366 |
rs368077618 | snp | A/T | 0.000280036 | 0.0118296 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102305245 | ATTCATTAGATATTG[A/T]CGACAGGCCTCATAG | 51366 |
rs368088028 | snp | G/T | 4.96635e-05 | 0.0049829 | intron-variant | UBR5 | GRCh38.p7 | 8:102361114 | TCTGTATCTTAGAGT[G/T]AATAATTTACCTCAA | 51366 |
rs368090310 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102284896 | AAAAAATTAGCCGGG[C/T]GTGGGTGGCAAGTGC | 51366 |
rs368094006 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102327423 | TGTAAAAGCAAAGTA[C/G]ATGTTTATGCAGAGG | 51366 |
rs368108255 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102287200 | AAAAAGGCAAGAAAA[A/T]AAAAATCTTTTAAAG | 51366 |
rs368153857 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102351196 | TGTCTGGTATATATT[C/T]GAAAGAATTGAAACC | 51366 |
rs368154671 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102393762 | TGGTGAAACTCCATC[C/T]CTACTAAAAACACAA | 51366 |
rs368173371 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102319718 | AGCAAATGTAAAAGA[A/T]CAGAAATTATAACAA | 51366 |
rs368186010 | snp | C/T | 3.45322e-05 | 0.0041551 | intron-variant | UBR5 | GRCh38.p7 | 8:102346424 | TAAAAAGAAGTGCTA[C/T]GGTAATTTTCTTTTG | 51366 |
rs368186911 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102357711 | GATCAATGTTAATTT[A/C]TTGGTTTTGATAATA | 51366 |
rs368196116 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102264602 | TAAATAATTCTAGAA[A/T]ACATATATCCCCCCA | 51366 |
rs368242285 | snp | C/T | 1.71737e-05 | 0.00293028 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102261915 | GTATATTTGCTTTAC[C/T]TGTCCTCCACCTTCT | 51366 |
rs368246076 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | UBR5 | GRCh38.p7 | 8:102288149 | TTTCTCAAATAACCT[G/T]CATACCGTCTTCATC | 51366 |
rs368246198 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102276343 | AGATTTTAATTTTTC[C/T]TCCTCCTCTTCCTTC | 51366 |
rs368332942 | snp | A/C/G | 0.000191798 | 0.00979104 | intron-variant | UBR5 | GRCh38.p7 | 8:102285076 | AAAAAATTGTAAGTT[A/C/G]AGGATCCATTTTAAG | 51366 |
rs368349736 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102356303 | AAAATACAAAACTTA[-/A]GTCAAGCGTGGTGGT | 51366 |
rs368505690 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102380399 | AAAAAAAAAAAAAAA[A/C]AAAAACAAAAACAAA | 51366 |
rs368516070 | snp | A/T | 1.65081e-05 | 0.00287293 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102277170 | TTCAGATTGGCAGCA[A/T]AAGACATTTTTGTTG | 51366 |
rs368517874 | snp | C/T | 0.000115814 | 0.0076088 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295055 | GTGCCACTTTGCTGA[C/T]TGAGGTATACTTGCT | 51366 |
rs368524641 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102257548 | ATTAAAATGACCAAC[C/T]ATTACAAACTTAAAA | 51366 |
rs368531269 | snp | C/T | 4.94466e-05 | 0.00497201 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102327810 | TAAAGAAACTATCCG[C/T]TCTCCTTGAAGTTCA | 51366 |
rs368537839 | snp | C/T | 1.65119e-05 | 0.00287327 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102300121 | ACCAGCTGCTCTCAA[C/T]GAACGTCTCATCATT | 51366 |
rs368548271 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102284837 | GTCAGGAGATCAAGA[C/T]CACCATGGCTAACAC | 51366 |
rs368572184 | in-del | -/CACACA | 0 | 0 | intron-variant | UBR5 | GRCh38.p7 | 8:102382862 | ACACACACACACACA[-/CACACA]GAGACACACACACTG | 51366 |
rs368647916 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBR5 | GRCh38.p7 | 8:102293511 | ACAAATGATCATGTA[C/T]ACCACCTGAGTGCTT | 51366 |
rs368652841 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102316797 | AGGAGAGAGAATGTC[A/G]GCTTAATAGCAAGGC | 51366 |
rs368687311 | snp | C/T | 0.00102535 | 0.0226191 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102412136 | GGAGGGAAGGGCGCC[C/T]CTCCCCCCGCGCCCG | 51366 |
rs368712774 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102383203 | ATCACATTCCTCTGA[A/C]GCCTGAGGGTAACGC | 51366 |
rs368715642 | snp | C/G | 1.64893e-05 | 0.0028713 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102281465 | CAGAGCATAATTTAG[C/G]AAGTCTCCTCGTGCA | 51366 |
rs368744218 | snp | C/T | 3.29821e-05 | 0.00406078 | intron-variant | UBR5 | GRCh38.p7 | 8:102267041 | TCACATTCCAGATAA[C/T]GGAGACTTCTAGAAT | 51366 |
rs368747506 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102334409 | CGATTCTCCCACCTC[A/C]GCCTCCCACGTAGCT | 51366 |
rs368768350 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102307361 | GACATCAAGTTCAGA[C/T]CACAGCTACCTCTGT | 51366 |
rs368786287 | snp | C/T | 0.000286256 | 0.0119602 | intron-variant | UBR5 | GRCh38.p7 | 8:102279229 | CATAAAAAGATAAAA[C/T]GTTTTGTTTTTTAGG | 51366 |
rs368793399 | snp | G/T | | | intron-variant, downstream-variant-500B, nc-transcript-variant | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102251855 | GCCTCCACCAAAGAC[G/T]TACTGAATCAGAAAG | 51366 |
rs368799122 | snp | C/T | 1.64787e-05 | 0.00287038 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102342529 | GACTTTGAACAGGTG[C/T]ATTCTTCTTATCCAA | 51366 |
rs368806590 | snp | A/G/T | 0.000116044 | 0.00761641 | intron-variant | UBR5 | GRCh38.p7 | 8:102295192 | TCTAAAAAGGTTTTA[A/G/T]TGAATACGTACGGGT | 51366 |
rs368809945 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102341900 | ATTCCTCAGGATACA[C/G]AGCATAACTCCCCTA | 51366 |
rs368831957 | snp | A/G | | | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295523 | TAAGAATAGTAAGAG[A/G]TGCTCTCCCCTGCAA | 51366 |
rs368852348 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102346511 | TAATCCCAGCACTTC[A/G]GGAGGCCAAGGTGGG | 51366 |
rs368903033 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102300950 | TTAGAACTAACAATG[A/G]TTTAAGAGAGCACAA | 51366 |
rs368908598 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102280241 | ACGCAAGAATGTGTA[A/C]GCAAAAATGGACAGA | 51366 |
rs368911444 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102319199 | GGAAACCCATCTCAC[A/G]TGCAGAGACACACAC | 51366 |
rs368946427 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102413545 | GGCGCGGTCTCGGCT[C/T]ACCTCAACCTCCGCC | 51366 |
rs368956161 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102350760 | TCAACAGACAACCTA[C/T]AGAATGAGAGAAAAT | 51366 |
rs368986138 | snp | A/G/T | 0.00438332 | 0.0466095 | intron-variant | UBR5 | GRCh38.p7 | 8:102317369 | ATCAAACCGCAAGGC[A/G/T]GCAGCCAGGCTGGGG | 51366 |
rs369059322 | in-del | -/GAG | | | intron-variant | UBR5 | GRCh38.p7 | 8:102291780 | CCATCTACTATTCAG[-/GAG]AATACAAAAAAAAAA | 51366 |
rs369075132 | in-del | -/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102274748 | AAAAAAAAAAAAAAA[-/G]AAAGAAATCTAAGAA | 51366 |
rs369136274 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102379981 | TTAGTAGAAAACTTC[A/G]TAACTGAAAATTTTA | 51366 |
rs369141589 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102336688 | CTTCTGGGCTCTCTA[C/T]TCTGTTCCATTGGTC | 51366 |
rs369157657 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102254182 | GTCTGCATTTTATCT[C/T]TTTAAGGTACCACCA | 51366 |
rs369169084 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102398906 | TAATAATGAGAATAT[A/C]TAAGGAGCTCAAACA | 51366 |
rs369175879 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102281843 | TTAGTAGGTCTGGGG[C/T]AAAGCCCCAGGATTT | 51366 |
rs369227718 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102411854 | TTACCGCCTGCCCCC[C/T]GGGAGCCAGAAACCA | 51366 |
rs369238749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102289024 | ACAAAAATTAGATGG[A/G]TGTGGTGGTGCGCGC | 51366 |
rs369251972 | in-del | -/AAT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102410094 | TTTTTAATGTTGTAT[-/AAT]GATAGAAGAATCAAA | 51366 |
rs369253008 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102325786 | GGAAAATAGATTTTC[A/T]AAAAAATAGTGGCGA | 51366 |
rs369253349 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBR5 | GRCh38.p7 | 8:102373352 | TAAGACTATATATAC[A/G]TTCATACAAGAATCA | 51366 |
rs369253732 | in-del | -/T/TT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102394623 | GATCTGCAGTTTTTT[-/T/TT]CCCAATAACAGTGAG | 51366 |
rs369277744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102405692 | GGTATGGTGGCGTGC[A/G]CCTGTACTCCCAGCT | 51366 |
rs369282402 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102402642 | GGAAAACACCCAAAT[C/G]AATTTCCACCATGTC | 51366 |
rs369287226 | snp | C/T | 0.000153988 | 0.00877327 | intron-variant | UBR5 | GRCh38.p7 | 8:102323531 | ACCATCAAGATGACA[C/T]AACTTTAAAAATATA | 51366 |
rs369312044 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102405543 | ATGTATAATATGGGC[A/G]AGCGCAGTGGCTCCC | 51366 |
rs369314978 | snp | A/C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102308910 | TCTCACATGTACTCC[A/C/G]AAGCCTAAAAGTTTT | 51366 |
rs369322500 | in-del | -/AG | | | intron-variant | UBR5 | GRCh38.p7 | 8:102392816 | ATGAGCCTGTTATCA[-/AG]GGTCTCCCCACAGCT | 51366 |
rs369326203 | snp | A/G | 0.000115434 | 0.00759631 | intron-variant | UBR5 | GRCh38.p7 | 8:102287398 | ACACACAGCCTTAGC[A/G]TAAGCAAGAAAGTAG | 51366 |
rs369338556 | snp | A/G | 1.6495e-05 | 0.0028718 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311836 | CTTTTCCTGTAGCAA[A/G]ATCAAAGATACAGTA | 51366 |
rs369363203 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102304859 | TAAAGTTCATTTAGC[A/G]TTACATATCCAGTTT | 51366 |
rs369462882 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102280530 | TGAACAGGAGCAAAA[C/G]TCAGAGGAAATACAA | 51366 |
rs369491472 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102398896 | GATAAGGGATTAATA[A/T]TGAGAATATCTAAGG | 51366 |
rs369492371 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102328879 | TGCTCGGATTACGGG[C/T]GTGAGCCACCAGGCC | 51366 |
rs369506011 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102378723 | TAATAACTCAATGTA[C/T]GCTGACTCAACAGAC | 51366 |
rs369523200 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102398116 | GCATGGTACTGGCAT[A/C]AAAACAGACACACAG | 51366 |
rs369530819 | snp | C/T | 1.65682e-05 | 0.00287817 | intron-variant | UBR5 | GRCh38.p7 | 8:102278978 | TAGTTACATTGAATA[C/T]TTTAAAGAAAATAAA | 51366 |
rs369531210 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102408112 | CGATTCTGCTCTGAA[C/T]GCTAAGGATATTCTA | 51366 |
rs369531406 | snp | A/C/G | 8.23681e-05 | 0.00641702 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102289507 | ATCTCTGCCCCGAAC[A/C/G]GGCTGTGACTGGCTG | 51366 |
rs369558238 | snp | A/G | 1.65111e-05 | 0.0028732 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102329287 | AAATAAAATACCTGG[A/G]CATTTCTGTAAGGCT | 51366 |
rs369566808 | snp | A/C | 3.37189e-05 | 0.00410588 | intron-variant | UBR5 | GRCh38.p7 | 8:102329444 | TAAAAATTGCCAAAT[A/C]TACTGATTTGAACAC | 51366 |
rs369589356 | snp | A/G/T | 7.11977e-05 | 0.00596611 | intron-variant | UBR5 | GRCh38.p7 | 8:102323287 | CTGGTGTCAAAGCAC[A/G/T]ATTAGTTAAGCTATA | 51366 |
rs369614399 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102374092 | GAACTACCACTTGTC[C/T]AGCAGTGATGCTGTA | 51366 |
rs369626847 | snp | A/G | 3.30611e-05 | 0.00406565 | intron-variant | UBR5 | GRCh38.p7 | 8:102360550 | ATATAATACCTAAGA[A/G]CTAAATACATATTAA | 51366 |
rs369640389 | in-del | -/AAAA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102408136 | ATTCTAGGGCAACTC[-/AAAA]TTTTGAGTTCCTGCT | 51366 |
rs369646358 | snp | C/T | 0.000165915 | 0.00910658 | intron-variant | UBR5 | GRCh38.p7 | 8:102311731 | AGCAAAAATGAGCCT[C/T]TACCTGTCCAGCAGT | 51366 |
rs369669982 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102347992 | AGCACTTTGAGAGGC[C/T]AAGGCAGGTGGATCA | 51366 |
rs369683004 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102395403 | CTATTTATATATATA[C/T]ACACACACACACGTA | 51366 |
rs369684687 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102290117 | ACCAAGAAAAGACAG[C/T]TGACTGGATTATAAA | 51366 |
rs369745735 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102381444 | GGGGAAACCACCCCC[A/G]TGATCCAATCACCTC | 51366 |
rs369786809 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102352196 | GCCTGTAGTCTCAGC[C/T]ACTTGGGGGGACTGA | 51366 |
rs369794797 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102286977 | TGAGCTCAGGAGCTC[A/G]AGACCAGCCTGGGCA | 51366 |
rs369796234 | snp | C/T | 0.000937568 | 0.0216311 | intron-variant | UBR5 | GRCh38.p7 | 8:102311693 | CTCACAAAAATGCCA[C/T]TGTTGTCCTATCACT | 51366 |
rs369796870 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102377445 | AGGCGTGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 51366 |
rs369798635 | snp | C/T | 4.98956e-05 | 0.00499453 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102298422 | GAGCAGTTTCTAAGA[C/T]GGTAATTGCAGCAGG | 51366 |
rs369814232 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBR5 | GRCh38.p7 | 8:102261679 | TACACTCCAGCCTGG[C/T]GACAGAGCAAGACTC | 51366 |
rs369820581 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102328184 | AGAATTTAGTGACTT[C/T]AGGCCAGGTGTCATG | 51366 |
rs369821325 | snp | A/T | 6.61015e-05 | 0.0057486 | intron-variant | UBR5 | GRCh38.p7 | 8:102295365 | GTGACCAAAACAAAA[A/T]TAAAACATATTGCTT | 51366 |
rs369821912 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102365806 | TTGCTAGAAGCCAAC[A/G]TATTTCATTGCTATA | 51366 |
rs369835669 | snp | C/T | 2.65298e-05 | 0.003642 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102345431 | GAAAGTGATGAACGA[C/T]GAAAAGAAGGGTAAC | 51366 |
rs369862910 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102341510 | CAGTAACCATGGAAA[C/T]GTAAATTTGGAAAGT | 51366 |
rs369884212 | in-del | -/ATA | 0.0573587 | 0.15934 | intron-variant | UBR5 | GRCh38.p7 | 8:102323085 | CCTACAACTTAAAGT[-/ATA]ATAATAATAAATTAA | 51366 |
rs369909197 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102292078 | GAACATAACAAGAAC[A/G]TTTTCAAGAGGTGGA | 51366 |
rs369912795 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102398730 | AGGTTGCAGTGAGGC[A/G]AGATCGCGCCACTGC | 51366 |
rs369915070 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102320188 | CAAAATTGATAGACC[A/G]CTAGCAAGACTAATA | 51366 |
rs369934081 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102266400 | AGGCAATCAACCTAC[A/T]TAGGTTCAAATTGGA | 51366 |
rs369942704 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102314476 | GATAGACTAGCTAGT[A/G]GCAATTATTTCCTTC | 51366 |
rs369956469 | snp | C/G | | | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102413035 | GTGTCCCAGAGGAGG[C/G]GAGGAGGAAGAGGGG | 51366 |
rs369966151 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | UBR5 | GRCh38.p7 | 8:102347866 | TGATCCACCCACCGT[G/T]GCCTCCCAAAGCGCT | 51366 |
rs369987149 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102358806 | GACGGGGGTCTCTCA[C/T]TTCCATTGCCCAGGA | 51366 |
rs369990662 | snp | A/C | 1.66123e-05 | 0.00288199 | intron-variant | UBR5 | GRCh38.p7 | 8:102288105 | TAATATCTCCCTTTA[A/C]AAGTACCTGATTTAC | 51366 |
rs370010399 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102310405 | GGGCTGGAGTTCAGT[A/G]GCGCGATCTCGGCTC | 51366 |
rs370037002 | snp | C/T | 0.00013293 | 0.00815153 | intron-variant | UBR5 | GRCh38.p7 | 8:102361099 | AGTTTATTTTTCATT[C/T]CTGTATCTTAGAGTG | 51366 |
rs370040269 | snp | A/T | 1.6654e-05 | 0.00288561 | intron-variant | UBR5 | GRCh38.p7 | 8:102272492 | TTGAGGAACAAGGAA[A/T]GAATTTTAAGCTGCT | 51366 |
rs370049960 | snp | C/G | 5.14575e-05 | 0.00507209 | intron-variant | UBR5 | GRCh38.p7 | 8:102293570 | ACATTTCCAGAGAAG[C/G]ATTAATCAGAATCTG | 51366 |
rs370114547 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102394622 | AGATCTGCAGTTTTT[-/T]TYCCMATAACAGTGA | 51366 |
rs370128758 | in-del | -/ATTAT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102335390 | ATAAAATGGTATCAT[-/ATTAT]GGATTTTTGTTAAGT | 51366 |
rs370133069 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102370926 | CCTGGCTCATCCATG[C/T]TGTTGCAAATGACAA | 51366 |
rs370138988 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102337384 | TCTGAGTTGCTCCCT[A/G]TTGATTGTTAGCTAT | 51366 |
rs370148532 | snp | A/G | 4.25849e-05 | 0.00461418 | intron-variant | UBR5 | GRCh38.p7 | 8:102297019 | TTTAAAGGAATAATT[A/G]TAAGTATGCATATAT | 51366 |
rs370169373 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102344308 | TTTAAGGATTTCAAA[-/T]CTTTTTTTTTTTTTT | 51366 |
rs370172527 | snp | A/C | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285163 | AAGCTAGCTTCTTCT[A/C]GCGCAGTCATCCTCT | 51366 |
rs370179058 | snp | A/G | 0.000115688 | 0.00760465 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102346246 | CCAACCTCCAGGCAA[A/G]TAAGATTCGCTGGCT | 51366 |
rs370181382 | snp | C/T | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102281353 | CCTTAATCCAGTATA[C/T]AAGTGCTTGAAAAAC | 51366 |
rs370243156 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102356323 | AGCGTGGTGGTGGGC[A/G]CCTGTAATTACAGCT | 51366 |
rs370270661 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102386596 | AAATTAACGTAGACA[A/G]AAGGTAACAGTTAAT | 51366 |
rs370295658 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102255971 | AAGATTGAGTCACTA[C/G]CAAATTTTTCTTTCA | 51366 |
rs370320731 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102344481 | ACCATGCTTGGCTAA[C/T]TGTTTTTGTATTTTT | 51366 |
rs370360165 | snp | C/T | 3.31472e-05 | 0.00407093 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285225 | AGGATGATTTGGATG[C/T]CCAGGATCACCAGCA | 51366 |
rs370384235 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102283823 | CTATTAGTTACTCAG[C/G]ATCAAGGTTTAAATA | 51366 |
rs370417081 | snp | G/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102305087 | TTCTTAATCTCACCC[G/T]CTTCTTCTTTAGTTT | 51366 |
rs370418348 | snp | C/T | 3.31098e-05 | 0.00406864 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102261234 | GGAGTGACTGGTATA[C/T]TTACACCATTAGGAA | 51366 |
rs370418877 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | UBR5 | GRCh38.p7 | 8:102275866 | GGTGGGGGGGAGAAA[G/T]AATTTAGCCAATTTC | 51366 |
rs370420055 | snp | C/T | 1.65806e-05 | 0.00287924 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102275812 | AAATAACCATTCCCA[C/T]AAAGCTACACTGTGG | 51366 |
rs370451609 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102269434 | ATCAGAGAGCCAGAA[A/G]TATCTTTTATTTAGG | 51366 |
rs370485767 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102287620 | TATGGTTTAAAACAG[C/G]GTCTGATAAGCCAGA | 51366 |
rs370486334 | snp | A/T | 0.000182279 | 0.00954496 | utr-variant-3-prime, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102254296 | GCAATACACACTTTT[A/T]ATACTCTACACAAAA | 51366 |
rs370507193 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102287215 | TAAAAATCTTTTAAA[A/G]AAACTTTAAAATTCA | 51366 |
rs370514304 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102262325 | CATAATAGTTTTAAA[C/G]TTCCAAAACTGCAAA | 51366 |
rs370518924 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102406813 | CTTTGTTATGCTTCA[C/T]ATAATCCCTGGCATA | 51366 |
rs370524211 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102307068 | GAATCAAATGCCTAC[A/G]CTTGAAGTAATATAA | 51366 |
rs370547223 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102367605 | AAGGAGATCTTTGTT[A/G]TAAGACCTCCTATAT | 51366 |
rs370661696 | snp | C/G | 1.65116e-05 | 0.00287324 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102294024 | ACTGAACGTAGAAAC[C/G]TCATTGTCACAGCAA | 51366 |
rs370662676 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102352097 | CGGATCACTTGAGGT[C/G]AGGAGTTCGGGACCA | 51366 |
rs370699852 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102296031 | TTGGAATCTCTTCCC[C/T]AATTCCCAGTCCTGT | 51366 |
rs370751124 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102382032 | TATAACAGTTTCCTT[A/G]TTTTACATTTGAGAA | 51366 |
rs370807056 | snp | G/T | 3.29516e-05 | 0.00405891 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102288178 | TCATGCTCATCATGT[G/T]GTCCCTCTGCCTCAG | 51366 |
rs370816873 | snp | C/G | 6.96852e-05 | 0.00590235 | intron-variant | UBR5 | GRCh38.p7 | 8:102277244 | GAAAAAAACTAATTA[C/G]ATTTTGTCCTCAACT | 51366 |
rs370830119 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102335711 | GTGCCACCATGCCCA[A/G]CTAGTTTTTGTATTT | 51366 |
rs370837296 | snp | C/T | 1.66059e-05 | 0.00288144 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285522 | TCATACCTGTAAGTT[C/T]ACTGCATCTTGGTAA | 51366 |
rs370841169 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102399343 | GCAATGGCGCGATCT[C/T]GGCTTACTGCAACCT | 51366 |
rs370841997 | snp | A/G | 3.30289e-05 | 0.00406366 | intron-variant | UBR5 | GRCh38.p7 | 8:102360669 | AACTCTACCATCCTA[A/G]AAGCAAAGAAAACAG | 51366 |
rs370843950 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102358007 | AAAAATTAGGAGGGC[A/G]TGGTGGCACGCGCCT | 51366 |
rs370851636 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102370239 | TGGTGTGATCTCAAC[C/T]CACTGCAGCCTCCGC | 51366 |
rs370856127 | snp | C/T | 1.77153e-05 | 0.00297612 | intron-variant | UBR5 | GRCh38.p7 | 8:102262095 | TAATCATATGAAACT[C/T]AGTTATGAAAGAAAC | 51366 |
rs370871454 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102282441 | TGGGAGGCCAAGGTG[A/G]GTGGATCACCTGAGG | 51366 |
rs370895434 | snp | A/G | 6.61387e-05 | 0.00575021 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102280465 | TCCAAGAGTTCTCGC[A/G]TCCTTTAAAAAGACA | 51366 |
rs370897451 | snp | C/G | 1.68895e-05 | 0.00290593 | intron-variant | UBR5 | GRCh38.p7 | 8:102346186 | AAATTCCACTCCCCA[C/G]TCGAAAGAGCACTCC | 51366 |
rs370932779 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102384229 | ATCAATCCTGCCTTT[C/T]TGGATGAAGAGCTCA | 51366 |
rs370935672 | snp | C/T | 0.00136008 | 0.0260421 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102412139 | GGGAAGGGCGCCCCT[C/T]CCCCCGCGCCCGCCG | 51366 |
rs370978082 | snp | A/G | 5.15176e-05 | 0.00507505 | intron-variant | UBR5 | GRCh38.p7 | 8:102346892 | CATTAAGTGTTCTAC[A/G]AGATCCATACCTGTG | 51366 |
rs371042590 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102389547 | AATAATAATATATGA[C/T]TGTTGTTTCACCCAT | 51366 |
rs371050105 | snp | A/G | | | synonymous-codon, nc-transcript-variant, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102277103 | TTCTTCTGGCAGCAC[A/G]GGCTGTTCTTCCCCT | 51366 |
rs371063830 | snp | C/G | 1.6916e-05 | 0.00290822 | intron-variant | UBR5 | GRCh38.p7 | 8:102346188 | ATTCCACTCCCCAGT[C/G]GAAAGAGCACTCCAG | 51366 |
rs371087245 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102327185 | GCCTCCGAAAGCCAC[G/T]GTGCCTGGGCCTAAC | 51366 |
rs371090910 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102351118 | CGGAACAACCACTTT[C/T]GGAAAACAATATGGA | 51366 |
rs371103365 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102361512 | ATCATATCAGGCTGC[C/T]GCCTAAATGAGTTTT | 51366 |
rs371165073 | snp | G/T | 1.74202e-05 | 0.00295124 | intron-variant | UBR5 | GRCh38.p7 | 8:102261906 | CAGAAAAGTGTATAT[G/T]TGCTTTACCTGTCCT | 51366 |
rs371167254 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102319400 | AACTATCCTAAATAT[A/T]TATGCACCCAATACA | 51366 |
rs371189065 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102332285 | CCTTGAACAACTGTA[C/G]CATTCTCATAACCGA | 51366 |
rs371202048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102354751 | ACAAATCTGACAATT[A/G]GCAAAATCTTCTAAG | 51366 |
rs371202395 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102289236 | ACCCTTAATCCTTAA[A/G]GACAAGTTTGTGTCC | 51366 |
rs371237301 | snp | C/T | 6.75744e-05 | 0.00581228 | intron-variant | UBR5 | GRCh38.p7 | 8:102257752 | ATAAAATATACTATA[C/T]CAGTTGTTGTTATTA | 51366 |
rs371248324 | snp | C/G | 0.000181268 | 0.00951847 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311481 | CATTTCCATCTCGAA[C/G]AATAATGGGAGATTC | 51366 |
rs371251435 | snp | C/T | 0.000153988 | 0.00877328 | missense, upstream-variant-2KB, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102304070 | GATGATCCAGCCCGA[C/T]TACCTGGGCCATTAC | 51366 |
rs371252437 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102354957 | AACATGGCAAAACCC[A/T]GCTCTACCAAAAATA | 51366 |
rs371279602 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | UBR5 | GRCh38.p7 | 8:102326935 | AGACGGGGCCTTTCT[C/G]TGCTGCCCAGGCTAC | 51366 |
rs371291715 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102350010 | CAACACATTGAGACC[C/T]GTCTCTACAAAAAAA | 51366 |
rs371301799 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102270667 | TGGGATTACAGGCAT[A/G]CGCCACCACACCTGG | 51366 |
rs371304773 | in-del | -/ACG | | | intron-variant | UBR5 | GRCh38.p7 | 8:102383103 | GTGGCCAGTGAGTTC[-/ACG]ACAAGAGAAAACTTT | 51366 |
rs371307995 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102352028 | AAAATCAACTATTGG[C/T]TGGGTGTGGTGGCTC | 51366 |
rs371317086 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102256600 | TATATCAAACCCACC[C/T]GGGGAACAAACTAAG | 51366 |
rs371401975 | in-del | -/A | 0.0759472 | 0.179459 | intron-variant | UBR5 | GRCh38.p7 | 8:102355527 | AATATGTGTGACTGT[-/A]AAAAAAAAAATTTGA | 51366 |
rs371417376 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBR5 | GRCh38.p7 | 8:102344906 | TGCATTCCAGCCTGG[A/G]CAACAGAGTGAGACT | 51366 |
rs371434039 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102306040 | CTCTTATGCTATTAA[A/C]GGTTATATGAAAACC | 51366 |
rs371484628 | snp | C/G | 0.000103783 | 0.00720282 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102412260 | TTCTCGTCCTCCACT[C/G]GAGGGCGGCCCCCTC | 51366 |
rs371491529 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | UBR5 | GRCh38.p7 | 8:102394210 | GGATTACATTCGCAC[A/G]CCACCACGCCCAGCT | 51366 |
rs371518006 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102347675 | CAGGGTCTCCCTCTG[C/T]CGCCCAAGCTGGGGT | 51366 |
rs371582365 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102407774 | GAAAAAAAAAAAGAA[C/G/T]GTATATTGCTTGAAA | 51366 |
rs371630086 | snp | C/T | 5.0847e-05 | 0.00504192 | intron-variant | UBR5 | GRCh38.p7 | 8:102285389 | AAATAGAGCTAAATT[C/T]GATACAGCAGCAGTA | 51366 |
rs371649846 | snp | A/G | 8.25008e-05 | 0.00642212 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102279066 | CTGATCAGCCAAGGG[A/G]ATGGCTTCAGCCAGA | 51366 |
rs371658192 | snp | C/T | 1.64775e-05 | 0.00287027 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102286527 | GTCTCCTGTTCTATG[C/T]CGTCACTCTGACTAC | 51366 |
rs371668878 | snp | A/G | 0.000166692 | 0.00912787 | intron-variant | UBR5 | GRCh38.p7 | 8:102342431 | GGGAGGGGTTGTCAG[A/G]GATCCATTTAAATGG | 51366 |
rs371673887 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102378710 | TTTTGCACCAACCTA[A/G]TAACTCAATGTACGC | 51366 |
rs371684381 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102259269 | CAAAAAAAATTCAGT[C/T]CTGTATTTTTTATTT | 51366 |
rs371698554 | snp | C/T | 3.35154e-05 | 0.00409348 | intron-variant | UBR5 | GRCh38.p7 | 8:102329427 | ATACAATACTATAAA[C/T]ATAAAAATTGCCAAA | 51366 |
rs371700554 | snp | A/G | 8.23716e-05 | 0.00641709 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102281390 | CACATGCTTCAATGA[A/G]CAAACATCCAAAACT | 51366 |
rs371713915 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102312746 | CAGTAATCAACTGAA[A/G]AACTTAAGTATATAG | 51366 |
rs371786980 | snp | A/G/T | 9.1466e-05 | 0.00676207 | intron-variant | UBR5 | GRCh38.p7 | 8:102323275 | GCAAACAAGGAACTG[A/G/T]TGTCAAAGCACGATT | 51366 |
rs371792950 | snp | A/G | 1.64762e-05 | 0.00287016 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102289540 | GCGCCTCTGCTGTGG[A/G]TTCCTGATGATGTAG | 51366 |
rs371824684 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102309412 | AAAGGTTAAAAAAAA[-/A]TTTAGTGTAGCCTAA | 51366 |
rs371853761 | snp | G/T | 1.65278e-05 | 0.00287466 | intron-variant | UBR5 | GRCh38.p7 | 8:102313936 | GACAACAACAAAATG[G/T]TAAGTACCAAAAAGA | 51366 |
rs371876387 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102355264 | GCAAAAGTGAGCAGG[C/T]CTAGACTCTGCAGGA | 51366 |
rs371892297 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102320079 | GCAGAAGGCAAGAAA[C/T]AACTAAAATCAGAGC | 51366 |
rs371924240 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102317097 | GGACAGTGGGTGCAA[C/T]GCACCGTGCACCAGC | 51366 |
rs371930779 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBR5 | GRCh38.p7 | 8:102402147 | CCTGGGCCTGGGAGA[C/T]TGAGATTGCAGTGAG | 51366 |
rs371941025 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102343098 | AACTTCAACATGTTA[C/T]GTATATAAGCAAACT | 51366 |
rs371974331 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295065 | GCTGATTGAGGTATA[C/T]TTGCTCTTCTGGCAA | 51366 |
rs371975946 | snp | G/T | 1.64963e-05 | 0.00287192 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102254389 | GAGTGGGACGTAAAG[G/T]CGAGAAATGCAAGTA | 51366 |
rs371979726 | snp | C/T | 0.000102464 | 0.00715693 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102412239 | ATGGACGTCATGGTG[C/T]TTTCCTTCTCGTCCT | 51366 |
rs371985441 | snp | A/G | 1.89457e-05 | 0.00307774 | intron-variant | UBR5 | GRCh38.p7 | 8:102286339 | TAAGTATTCTTAGCA[A/G]TACTAAGTTTTCAGA | 51366 |
rs371997729 | snp | C/G | 4.98219e-05 | 0.00499084 | intron-variant | UBR5 | GRCh38.p7 | 8:102305332 | GAAAAAAACCTCAAT[C/G]AATTTGAGTAGCACA | 51366 |
rs372005747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102301200 | TGCAATTATTATTTA[A/G]TTGAGGATAAATGTG | 51366 |
rs372013099 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102351402 | CATTATGATAACTGA[A/C]ATAAGCCTGTCACAC | 51366 |
rs372014119 | snp | C/T | 1.84903e-05 | 0.00304053 | missense, intron-variant | UBR5 | GRCh38.p7 | 8:102361592 | CTTACCTGTTTAAAT[C/T]ATATTTGTTCAGCTT | 51366 |
rs372017878 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102256144 | AACCCTGTCTCTACT[-/A]AAAAATACAAAAAAT | 51366 |
rs372018359 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102404584 | CAAGTGACTGCTGAC[A/T]AAAAATGCTGTCATA | 51366 |
rs372070228 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102389757 | TTCTTCCTATTAATA[A/T]TAAGGATTTTTTTTT | 51366 |
rs372070744 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102346645 | CATTAATTCCAGCTA[C/T]TCGGGAGGCTGAGGC | 51366 |
rs372074479 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102280604 | CAAACATTTTCAGAA[G/T]CTGGGAAATGGTAGA | 51366 |
rs372075147 | snp | A/G | 1.67773e-05 | 0.00289626 | intron-variant | UBR5 | GRCh38.p7 | 8:102329431 | AATACTATAAATATA[A/G]AAATTGCCAAATCTA | 51366 |
rs372076404 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102368836 | TAACACAGTTGCCTC[A/G]GCAGCTTCCTTTCTT | 51366 |
rs372119369 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102356650 | CTGTAGTCCCAGCTA[C/T]TCGAGAGGCTGAGGC | 51366 |
rs372173531 | snp | C/T | 4.9543e-05 | 0.00497685 | intron-variant | UBR5 | GRCh38.p7 | 8:102288292 | AATCTTATTTGTAGA[C/T]AATCAAAGCTAGTTA | 51366 |
rs372182084 | snp | A/G | 0.000115427 | 0.00759606 | intron-variant | UBR5 | GRCh38.p7 | 8:102267042 | CACATTCCAGATAAC[A/G]GAGACTTCTAGAATT | 51366 |
rs372183951 | snp | A/G | 1.66208e-05 | 0.00288273 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102314775 | ACTGCTGGCAATTGA[A/G]GATGCATCACTACAC | 51366 |
rs372205803 | snp | A/C/G | 6.71699e-05 | 0.00579494 | intron-variant | UBR5 | GRCh38.p7 | 8:102280362 | AGGCAGCCATTTCTT[A/C/G]AAGTAGATTAGCAGA | 51366 |
rs372229553 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303154 | CTTCCCACTTTAGAC[C/G]AAACACTTTGTCTGC | 51366 |
rs372236540 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102328010 | GAGTTCTAAAATGTT[G/T]TGAGTTAAATGCTAT | 51366 |
rs372239875 | snp | A/G | 4.99729e-05 | 0.0049984 | intron-variant | UBR5 | GRCh38.p7 | 8:102281522 | CAAGGTGGCACGTCT[A/G]TAAGAACAGAAAGGA | 51366 |
rs372258153 | snp | C/G/T | 8.67211e-05 | 0.00658437 | intron-variant | UBR5 | GRCh38.p7 | 8:102285099 | ATTTTAAGTTGGGGA[C/G/T]GTTCTGTATATATGA | 51366 |
rs372324475 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102256281 | GCACTCCAGCCTGAG[C/T]GACAGAGTGAGACTC | 51366 |
rs372372648 | snp | A/C/G/T | 0.000422858 | 0.0145359 | intron-variant | UBR5 | GRCh38.p7 | 8:102275854 | TTTAAGGGAAGGGGT[A/C/G/T]GGGGGGAGAAATAAT | 51366 |
rs372374643 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102394030 | CTTATTTTAGGTGAA[C/T]AGTTAAATAAGCTAA | 51366 |
rs372378341 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102294096 | TCTTTCACTAGTGTA[C/T]CTAGTAGAGTATCTA | 51366 |
rs372442217 | snp | A/C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102386030 | TCTAATATGATGTGC[A/C/G]TAGTCCACCATCTCA | 51366 |
rs372492097 | snp | A/G | 1.66358e-05 | 0.00288402 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102261249 | TTTACACCATTAGGA[A/G]TGAGTTCAACCTGTG | 51366 |
rs372504688 | snp | C/G | 3.55076e-05 | 0.00421338 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102312139 | CAAAATTTACCTTTG[C/G]AATCTACATTCACTG | 51366 |
rs372511084 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102380405 | AAAAAAAAACAAAAA[A/C]AAAAACAAAACACAC | 51366 |
rs372525669 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102284162 | TGATACCTACTCCTG[A/G]AAAAGGTCACTTTAT | 51366 |
rs372563520 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102393965 | TTCTAGAGGAAAAAA[A/T]ATTTTAGGTGAAACT | 51366 |
rs372596745 | in-del | -/TC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102399967 | AAAAAAAAAAAAAAA[-/TC]AAAAATGCACATGGG | 51366 |
rs372600327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102317602 | TAGTTCTCCCAGCGT[A/G]CAGCTGGAGATCTGA | 51366 |
rs372619166 | snp | A/G | 0.000346726 | 0.0131622 | intron-variant | UBR5 | GRCh38.p7 | 8:102360207 | TGGGGGAAAGCAAGA[A/G]GTAAATTTTTGAAGA | 51366 |
rs372638217 | in-del | -/CTCA | 0.00874735 | 0.0655527 | intron-variant | UBR5 | GRCh38.p7 | 8:102261748 | TCTACCTCAGTCTGT[-/CTCA]CTAACTCTTGATCCA | 51366 |
rs372641640 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102376844 | ATTTTTTTAAAAAAA[C/T]GTCTATGCATCCACA | 51366 |
rs372653318 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102400193 | CCTAGCTACTTGTCT[A/G]TAATCCCAGCTACTC | 51366 |
rs372658524 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102356388 | CCAGAAGCAGAGGTT[G/T]CAGTGAGCTGAGATC | 51366 |
rs372661722 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102270427 | TATCAAGAGTCCACA[C/T]ATAATTCTGGAAATT | 51366 |
rs372687240 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102344077 | TCCTAAGTACTAAAA[C/G]TATATGCAGCAAGCT | 51366 |
rs372689227 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102366557 | AACTCTCCAGGTCTT[C/T]CGTCTCAAATTAAAT | 51366 |
rs372703845 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102309239 | TTTGTATTTTTTGTA[A/G]AGACAGGGTTTCGCT | 51366 |
rs372714156 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102307938 | GACTTAGTCCTTGGA[C/T]CTTTTCTCCTCACCA | 51366 |
rs372719596 | snp | C/T | 0.00030495 | 0.0123443 | intron-variant | UBR5 | GRCh38.p7 | 8:102295786 | GTCCGTTTGAGTCTA[C/T]AGAGAATTTATACAC | 51366 |
rs372812946 | snp | G/T | 1.66349e-05 | 0.00288395 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311883 | GTCTTCAGAACAGCA[G/T]GAACACCTTCAGAAG | 51366 |
rs372814978 | snp | A/C | 3.41198e-05 | 0.00413022 | intron-variant | UBR5 | GRCh38.p7 | 8:102261132 | ATCACACAACACTTT[A/C]TAGAAACACTTACAT | 51366 |
rs372818108 | in-del | -/C | 0.00398564 | 0.0444627 | intron-variant | UBR5 | GRCh38.p7 | 8:102309875 | CCCCTGGGTAAGTCA[-/C]TATCATCTCCCACCT | 51366 |
rs372827148 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102326196 | AGAGCAGTATCTTTC[A/C]AACGGGTTAGTCATA | 51366 |
rs372833490 | in-del | A/GG | | | intron-variant | UBR5 | GRCh38.p7 | 8:102283350 | GGAAGGCGGGGGGGG[A/GG]GGGGGTGAGTAGGGG | 51366 |
rs372944284 | in-del | -/T | 0.0577344 | 0.159793 | intron-variant | UBR5 | GRCh38.p7 | 8:102283729 | TTGACATTTCTACCA[-/T]TTTTTTTCCCCCAGT | 51366 |
rs372986438 | in-del | -/GTTT | | | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102252929 | GTAAAGTGACTGTTT[-/GTTT]TAAGTCACTTCATTG | 51366 |
rs372993333 | snp | C/G/T | 6.77356e-05 | 0.00581927 | intron-variant | UBR5 | GRCh38.p7 | 8:102279235 | AAGATAAAATGTTTT[C/G/T]TTTTTTAGGAAAATT | 51366 |
rs373005757 | snp | C/T | 1.70965e-05 | 0.00292369 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102304216 | AAGTTTTAGAACTAA[C/T]ACACTGAGTATGTAT | 51366 |
rs373017857 | snp | A/G | 1.65765e-05 | 0.00287888 | intron-variant | UBR5 | GRCh38.p7 | 8:102269111 | TACTTGCAAATGCCT[A/G]TAAATGATGAACAAA | 51366 |
rs373034975 | snp | A/G | 1.65743e-05 | 0.00287869 | intron-variant | UBR5 | GRCh38.p7 | 8:102295335 | CATATCTGAATCTAA[A/G]ATGAAAAAGAAATAG | 51366 |
rs373042512 | in-del | -/C | | | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303573 | TAGTCAAATACCTAG[-/C]AATTTTTAATGTGTT | 51366 |
rs373045256 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102391280 | GTAAAAATTACTCCA[C/T]GATAAAATTCAAATG | 51366 |
rs373097910 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102348028 | TCAGGAGTTCAAGAC[C/T]AGCCTGGCCAACATA | 51366 |
rs373105355 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102371658 | CAATGGCACGATCTC[A/G]GCTCACTGCAACCTC | 51366 |
rs373105695 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102414151 | CTGTTTTTTTTTCCC[C/T]AAGGAACCAATTCAT | 51366 |
rs373108483 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102383454 | AAAGCTGTCTGCTGA[A/C/G]ATCAGTAATCAGCCC | 51366 |
rs373133116 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102323801 | AAACCTCCGTCTCTA[C/T]TAAAAATACAAAAAT | 51366 |
rs373133614 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102366031 | CAGATCCTTTCTTGC[A/T]GAATTTCTAAAGCAA | 51366 |
rs373133667 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102373117 | CCTGAGAGCTGGGAT[A/T]ACAGGTGTGAGCCAC | 51366 |
rs373143877 | snp | A/G | 1.66651e-05 | 0.00288657 | intron-variant | UBR5 | GRCh38.p7 | 8:102326501 | GAAGAAAGTGATTCT[A/G]AAGAGAAACGAGGTC | 51366 |
rs373160357 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102380254 | CAAATATTAGCCACA[C/T]ATGGTGGTACACGCC | 51366 |
rs373174288 | snp | A/G | 1.66018e-05 | 0.00288108 | intron-variant | UBR5 | GRCh38.p7 | 8:102259135 | TCCTCATTGCCTAGA[A/G]AATTTCAGAAACAAT | 51366 |
rs373191255 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102331020 | ACCTTAATGGTAATC[C/T]GCTTCCACTTAATGA | 51366 |
rs373211938 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102287075 | CCAGCTACTCAGGGG[A/G]CTGAGGTAGGAGCTC | 51366 |
rs373217018 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102317862 | TAGCAAACTCCAACA[C/G]ACCTGCAGCTGAGGG | 51366 |
rs373239980 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102262639 | GGAACACTTTAAGAA[C/T]TTAATAGGGTCAGAG | 51366 |
rs373315207 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102337723 | GATATTATTAGCCTA[C/T]GGTTTTCTTTTCCTC | 51366 |
rs373327810 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | UBR5 | GRCh38.p7 | 8:102321385 | CCAACTTACAAGGGA[C/T]GTGAAGGACCTCTTC | 51366 |
rs373345353 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102412842 | CGGCAAGGCCCCCTC[A/G]ATTGGGCTGCTCAAC | 51366 |
rs373367257 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | UBR5 | GRCh38.p7 | 8:102275635 | CTTAAAAAAAAAAAA[A/G]TGCATGACAGATTAT | 51366 |
rs373368431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102313463 | TTAAATGTCATGGAA[A/G]ATGATCTCAACTAGA | 51366 |
rs373379028 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102341810 | ACTCTGTTTCACTTA[C/T]GGCAGTGATGGATTT | 51366 |
rs373381990 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102358413 | AGGCTATACTTTACT[A/G]ATCCTTAAACTAAAC | 51366 |
rs373396628 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102398898 | TAAGGGATTAATAAT[C/G]AGAATATCTAAGGAG | 51366 |
rs373400567 | snp | A/G | 9.91113e-05 | 0.00703888 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285187 | ATCCTCTCTCTTCTC[A/G]CTGAATTCTGAGAAG | 51366 |
rs373471759 | in-del | -/GT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102307771 | CACTTGACACAGTTG[-/GT]CCCAACATCCTGCTT | 51366 |
rs373501184 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102378656 | CTTGAAAAAAGGAGG[-/A]AAAAAAAAAAAAAAA | 51366 |
rs373596422 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102388549 | GAGTAACGTGCTGAT[A/G]ACGTCATAACAAGAT | 51366 |
rs373619424 | snp | C/T | 1.78828e-05 | 0.00299017 | intron-variant | UBR5 | GRCh38.p7 | 8:102314712 | CTGCATGAGACCTAT[C/T]TTCACAAATGCATAC | 51366 |
rs373623343 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102293530 | ACCTGAGTGCTTATG[C/T]AAAGGTTTTAGGAAG | 51366 |
rs373637935 | snp | A/G | 4.95111e-05 | 0.00497525 | intron-variant | UBR5 | GRCh38.p7 | 8:102295543 | CTCCCCTGCAAAACA[A/G]AATGTTGTCGTGAGG | 51366 |
rs373639807 | snp | C/T | 0.000164731 | 0.00907405 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102281387 | TGCCACATGCTTCAA[C/T]GAGCAAACATCCAAA | 51366 |
rs373642894 | in-del | -/TTTA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102254978 | AAAGCAAAAAAAGTA[-/TTTA]CTGCTACATTGTGAT | 51366 |
rs373644294 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102266506 | TGTTTTTGCAATGTT[A/G]GCACCAGCTACTTCT | 51366 |
rs373668536 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102382499 | TCAAAAAAGGAAATA[C/T]AACACAAGGGTAGAG | 51366 |
rs373683653 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102279763 | TTGTTTGCGTATAAA[C/T]GGCAGTGAGCTATGG | 51366 |
rs373691523 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102334395 | CTCCTGCGTTCCAGC[A/G]ATTCTCCCACCTCAG | 51366 |
rs373693727 | snp | A/G | 3.30175e-05 | 0.00406296 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102280441 | GAATCTTCATTATCA[A/G]TACCCAGTTCCAAGA | 51366 |
rs373699829 | snp | C/T | 5.02239e-05 | 0.00501093 | intron-variant | UBR5 | GRCh38.p7 | 8:102311697 | CAAAAATGCCATTGT[C/T]GTCCTATCACTTTTC | 51366 |
rs373767655 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102379291 | AAATGTTTGTAAAAC[A/G]CGGTCGCCATCATCA | 51366 |
rs373769382 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102256216 | GCTGAGGCAGGAGAA[A/T]GGCGTGAACCCGGGA | 51366 |
rs373775917 | snp | G/T | 1.65162e-05 | 0.00287365 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102294036 | AACCTCATTGTCACA[G/T]CAATAGCTTCTTCTC | 51366 |
rs373786248 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102284437 | AATAAAAAGGCTTTA[A/G]TATCAGATTCCTACG | 51366 |
rs373798138 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102359023 | TCAACAGATCCACTC[A/C]CCTTGGCCTCCCAAC | 51366 |
rs373798932 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102339295 | GCACTTTGGGAGGCC[A/G]AGGAGGGTGGATCAC | 51366 |
rs373819998 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102255696 | AACTCTGGAAACCCT[A/G]TAAGTTGCAGGACTA | 51366 |
rs373868809 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102298609 | TTCACATATAAATAT[A/T]CACCTCAATCAAACT | 51366 |
rs373875936 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102307723 | TAAATCCAACAGTCA[A/G]TATTCAGTATTCACT | 51366 |
rs373891014 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102270313 | TACCTAGGTGGTAGA[C/G]TGCCAAAACAGATGA | 51366 |
rs373896692 | in-del | -/AAACAAAC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102282172 | AGACCCTGTCTCAAA[-/AAACAAAC]AAACAAACAAACAAA | 51366 |
rs373966918 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | UBR5 | GRCh38.p7 | 8:102371054 | CCTATCTTGGCTATT[G/T]TGACTAGTGCTGCGA | 51366 |
rs373980266 | snp | A/G | 0.000135101 | 0.0082178 | intron-variant | UBR5 | GRCh38.p7 | 8:102346189 | TTCCACTCCCCAGTC[A/G]AAAGAGCACTCCAGA | 51366 |
rs374062631 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102361380 | CATTTATATCTCCCT[A/G]TATGCCAGATTTAAA | 51366 |
rs374123250 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102382100 | TTACTCAGTTAAGAG[G/T]AAAGTGGGAAAGAAG | 51366 |
rs374136727 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102411870 | GGGAGCCAGAAACCA[-/C]CCCCCCATCTCCGCC | 51366 |
rs374147773 | snp | G/T | 9.0007e-05 | 0.00670786 | utr-variant-3-prime, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102254254 | AAATGGAAAAAAATC[G/T]ACAAAATTTGCTAGT | 51366 |
rs374159239 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102275753 | GAATACCCTGCCGAA[C/T]AGTTCTAAAGAAAGG | 51366 |
rs374159936 | multinucleotide-polymorphism | CG/TT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102362976 | CGTGCCTCAGCCTCC[CG/TT]AGTAGCTGGAATTAC | 51366 |
rs374183428 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102381464 | CCAATCACCTCCCAT[A/C]GTGTCCCTCCCTTGA | 51366 |
rs374229186 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102327265 | ATATTGTTTCCAAAA[C/T]GCAATTTTGCTGTTA | 51366 |
rs374230100 | snp | C/T | 1.72068e-05 | 0.00293311 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102345489 | TGGCATCTGCATCAA[C/T]AATGACACTTGGGTG | 51366 |
rs374234004 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102287195 | AAAAAAAAAAGGCAA[A/G]AAAATAAAAATCTTT | 51366 |
rs374247845 | in-del | -/ACAC | 0.35207 | 0.228214 | intron-variant | UBR5 | GRCh38.p7 | 8:102382826 | GAAAATCACATTAAA[-/ACAC]ACACACACACACACA | 51366 |
rs374297079 | snp | C/G | | | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102413053 | GGAGGAAGAGGGGCT[C/G]TTGTGTTCTTTCGCT | 51366 |
rs374313356 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102288616 | GCAGGAGAATTGCTT[G/T]AACCCGGGAGGTGGG | 51366 |
rs374369689 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102375861 | CTGGTGAAGTGCCTT[A/G]ACATGAAAATTATAG | 51366 |
rs374420085 | snp | C/G | 1.64887e-05 | 0.00287125 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102272716 | ACATCTTCGACCAAA[C/G]TGATTGTTAAGCTGC | 51366 |
rs374453488 | snp | C/G | 1.69384e-05 | 0.00291014 | intron-variant | UBR5 | GRCh38.p7 | 8:102293589 | AATCAGAATCTGTTA[C/G]CTGGTAGCAATTTAC | 51366 |
rs374469435 | snp | C/T | 0.000391033 | 0.0139773 | intron-variant | UBR5 | GRCh38.p7 | 8:102327713 | TACACAAGCATTCAC[C/T]GATAAATTCCTCCTC | 51366 |
rs374544914 | snp | A/T | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102277040 | TAAGCTACTTTTTAA[A/T]TGTGCAGCAAGATCA | 51366 |
rs374547271 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102364409 | CTTGTCTTAAACTCC[-/T]GGGCTCAACGGATCT | 51366 |
rs374548431 | snp | C/T | 1.70342e-05 | 0.00291836 | intron-variant | UBR5 | GRCh38.p7 | 8:102294951 | AAAACATACTTTTCA[C/T]GTACTTGTAATACAC | 51366 |
rs374555108 | snp | C/T | 3.35312e-05 | 0.00409444 | intron-variant | UBR5 | GRCh38.p7 | 8:102329429 | ACAATACTATAAATA[C/T]AAAAATTGCCAAATC | 51366 |
rs374563504 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102256695 | AACCCATCTCACCAT[A/G]GCAGAGAAATATTAG | 51366 |
rs374573467 | in-del | -/AAA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102369937 | TGTCAAAATGGTGAA[-/AAA]GCCTCCGTTTTATTA | 51366 |
rs374576598 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102406146 | TTATAAAATTGCTCT[A/G]CCTTTGTTTTGATTT | 51366 |
rs374587398 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | UBR5 | GRCh38.p7 | 8:102285466 | ATTCTCATAATTGAC[A/G]GCCAAAAAAAAATAG | 51366 |
rs374597333 | snp | A/T | 1.65206e-05 | 0.00287403 | intron-variant | UBR5 | GRCh38.p7 | 8:102360559 | CTAAGAGCTAAATAC[A/T]TATTAAATAGAAAGG | 51366 |
rs374597724 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102352583 | ATTTCACTCAAAAAC[A/G]TCCCTGTTCAGACAA | 51366 |
rs374616318 | snp | C/T | 8.68282e-05 | 0.00658836 | intron-variant | UBR5 | GRCh38.p7 | 8:102361246 | TAAATTATTTTTTAA[C/T]GGTAAATACATCATA | 51366 |
rs374710935 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102265667 | ATCACTGTTTCCCTA[C/T]AGGTAAAGAACCATT | 51366 |
rs374733122 | snp | G/T | 6.76933e-05 | 0.0058174 | intron-variant | UBR5 | GRCh38.p7 | 8:102265094 | CCAAGATTAAAGTTC[G/T]TTTACCTGCCAATGT | 51366 |
rs374806308 | in-del | -/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102386993 | AAAAAAAAAAAAAAA[-/G]ACCTGTACTCAGGGA | 51366 |
rs374819680 | snp | C/T | 1.64855e-05 | 0.00287097 | intron-variant | UBR5 | GRCh38.p7 | 8:102266921 | AAATTCTGTGATTAT[C/T]AGCACATGAATAAAA | 51366 |
rs374871594 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102320109 | CAGAATTGAAGGAAA[C/T]AGAGACACAAAAAAC | 51366 |
rs374928444 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102393441 | AGAGTTCGAGACCAG[C/T]GTGGCCAACATGGTG | 51366 |
rs374983434 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102407024 | GGTAGTGAGTAGCTA[C/T]GTGGCACTACAGTGC | 51366 |
rs374999760 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102260408 | AATAATGTATACATG[C/T]TGATACATTTCACTA | 51366 |
rs375048398 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | UBR5 | GRCh38.p7 | 8:102257725 | ATTTTCTCCTAAGAA[C/T]GAAGAATGTAAATAA | 51366 |
rs375073200 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UBR5 | GRCh38.p7 | 8:102256172 | GCCAGGCGTGGTGGC[A/G]GGCACCTGTAGTCCC | 51366 |
rs375077487 | snp | A/G | 1.65754e-05 | 0.00287879 | intron-variant | UBR5 | GRCh38.p7 | 8:102295180 | GAAATACATAAATCT[A/G]AAAAGGTTTTAATGA | 51366 |
rs375121811 | snp | A/G | 0.00011901 | 0.00771304 | intron-variant | UBR5 | GRCh38.p7 | 8:102259170 | CTTCATTTTCCATGT[A/G]ACATTTATTTATATT | 51366 |
rs375124358 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102403087 | AGTGGACTTTTCCTA[C/T]GAAAAACATTGTGAT | 51366 |
rs375131598 | snp | C/G | 0.000757781 | 0.0194503 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102412164 | CCGCCGACCCGCCAG[C/G]CCTATTACCTGTCAT | 51366 |
rs375146384 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102398901 | GGGATTAATAATGAG[A/G]ATATCTAAGGAGCTC | 51366 |
rs375152063 | snp | A/T | 6.72744e-05 | 0.00579937 | intron-variant | UBR5 | GRCh38.p7 | 8:102329441 | ATATAAAAATTGCCA[A/T]ATCTACTGATTTGAA | 51366 |
rs375169553 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102347884 | CTCCCAAAGCGCTGC[A/G]AAAATAATTTTTTAA | 51366 |
rs375170763 | in-del | -/AAAC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102329929 | AAGGGAAAAAAAGAA[-/AAAC]AGAATACGGAGCTGA | 51366 |
rs375182479 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102292910 | AGATCAAATCCAAGC[A/G]TAACAACTTGGGAAC | 51366 |
rs375186861 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102322593 | TCCCATTACTGGGTA[C/T]ATACCCAAAGGACTA | 51366 |
rs375230849 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102334282 | AATAGATCCAGAACA[C/G]TAAGGAATATTAATG | 51366 |
rs375242653 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102405646 | CAACACGGTGAAACC[A/C]CATCTCTACTAAAAA | 51366 |
rs375257842 | snp | C/T | 8.30875e-05 | 0.00644491 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102314790 | GGATGCATCACTACA[C/T]GTGGATGCTGGAGAT | 51366 |
rs375262233 | snp | C/T | 4.97822e-05 | 0.00498885 | intron-variant | UBR5 | GRCh38.p7 | 8:102288317 | TAGTTAACTAAAATG[C/T]GAAGACCACTAACTA | 51366 |
rs375265370 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102332397 | ACCCCACCAATCACA[G/T]CAAGTCACTTCTCTA | 51366 |
rs375275462 | snp | C/T | 3.32375e-05 | 0.00407647 | intron-variant | UBR5 | GRCh38.p7 | 8:102312315 | CAGTTCCAATATTCA[C/T]TTGCTGAATAACTTC | 51366 |
rs375280443 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102288193 | TGTCCCTCTGCCTCA[A/G]CATTTTCTTCCCCGT | 51366 |
rs375280861 | snp | C/T | 1.65499e-05 | 0.00287657 | intron-variant | UBR5 | GRCh38.p7 | 8:102271084 | TCATTTACAGGCCTA[C/T]CTCTAATTCATCCAA | 51366 |
rs375287861 | snp | A/C | 3.29603e-05 | 0.00405944 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102277130 | CCCTTCTTTTTTTTG[A/C]CGGTTTTGCATGTTC | 51366 |
rs375296953 | snp | C/T | 0.000478039 | 0.0154529 | intron-variant | UBR5 | GRCh38.p7 | 8:102289587 | TGGAGCTGTAAAGAA[C/T]CAGAAGCTTATGAGT | 51366 |
rs375316071 | snp | A/G | 3.39432e-05 | 0.00411952 | intron-variant | UBR5 | GRCh38.p7 | 8:102281549 | AGGAAAATGTTTATT[A/G]GAAGAATACAAATGT | 51366 |
rs375349226 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102346914 | ATACCTGTGAAATCA[A/G]CTCCTCTGGAATGAC | 51366 |
rs375357944 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102350511 | GCTGGGAAAAGTGGA[C/T]ATCCACATGCAAAAG | 51366 |
rs375387541 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102386299 | GCTGGGTGTGGTGAT[A/G]CACGCCTGTAATCCT | 51366 |
rs375390367 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102316790 | TTAAACAAGGAGAGA[C/G]AATGTCGGCTTAATA | 51366 |
rs375393746 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102369224 | TAGATAGAAAAGTTA[A/C]GGAAAAGTGAGGTAC | 51366 |
rs375400419 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102394088 | TCTTTTTCTTGAGAC[A/G]GACTCTCGCCCTCGC | 51366 |
rs375477070 | snp | C/T | 3.30333e-05 | 0.00406393 | intron-variant | UBR5 | GRCh38.p7 | 8:102278817 | GCAAAAAAACTTTTA[C/T]TGTCTTACCTCTAGG | 51366 |
rs375479713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102273720 | CATTAAAGTGCAGTA[C/T]ATTAAGCAGCTATAA | 51366 |
rs375483211 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | UBR5 | GRCh38.p7 | 8:102329244 | TTTATATGTTGATAT[A/G]TAGAGCTATTCAATG | 51366 |
rs375516261 | snp | C/T | 6.81303e-05 | 0.00583614 | intron-variant | UBR5 | GRCh38.p7 | 8:102299567 | CAGTAAACAGAACAG[C/T]AGGATGTATATCATT | 51366 |
rs375533087 | snp | A/T | 1.70825e-05 | 0.00292249 | intron-variant | UBR5 | GRCh38.p7 | 8:102326711 | GCAGTAAAACAGCCC[A/T]CTAAATAAATCTGAA | 51366 |
rs375542965 | snp | A/C/T | 8.32952e-05 | 0.00645296 | missense, upstream-variant-2KB, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102304160 | GTATTTCTTTCAGAA[A/C/T]GCTCCGCTTCTGAAA | 51366 |
rs375549025 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102402815 | AGAGCCAATTTCTTG[A/C]AACGGCAGGTTCTCG | 51366 |
rs375560071 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102273080 | ATACCAAATGATCAG[A/G]GATGTTAAAAAAAAA | 51366 |
rs375567787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102356816 | AAATGGGGTAGAGGA[A/G]GGAAAGTTCTTCCTT | 51366 |
rs375590138 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102252473 | TCAAATGTCCTAATC[A/G]TATCTAGTTTGTTCT | 51366 |
rs375612623 | snp | A/C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102351178 | TATGATCCAGCAATT[A/C/G]CATGTCTGGTATATA | 51366 |
rs375649131 | snp | A/G | 5.00171e-05 | 0.0050006 | intron-variant | UBR5 | GRCh38.p7 | 8:102360716 | AAAAATGTGTATTAA[A/G]ATTTGAATTTATTCA | 51366 |
rs375659844 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102288006 | ATAGCGCCTAAATTT[C/T]CTAAATAGATGCTAC | 51366 |
rs375660372 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102299477 | GGAGGTGCTTGGTCC[C/T]TGACCAGTACCGGTT | 51366 |
rs375663363 | snp | A/C/T | 6.74895e-05 | 0.0058087 | intron-variant | UBR5 | GRCh38.p7 | 8:102285377 | TTAAAACTATCCAAA[A/C/T]AGAGCTAAATTCGAT | 51366 |
rs375685309 | snp | A/G | 5.16187e-05 | 0.00508003 | intron-variant | UBR5 | GRCh38.p7 | 8:102298380 | ACTCATTTAGGATCT[A/G]AAATAAATTACCTTT | 51366 |
rs375693537 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102362555 | GAATTCTGCTCTCTA[A/G]AGAGTCACAAAAATG | 51366 |
rs375704330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102319413 | ATATATGCACCCAAT[A/G]CAGGAGCACCCAGAT | 51366 |
rs375705977 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102348726 | GTTCCTACCGTACTC[A/G]CCTAAGGCTGAAACC | 51366 |
rs375708985 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102345336 | CAGTAGATTCTACCA[C/G]TATCTTTCCATACAG | 51366 |
rs375768889 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102288246 | ATCCTCTTCTCCAGC[C/T]ACACCCTCCACCACC | 51366 |
rs375789483 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102291911 | GACAAACTAGAATGA[C/T]AGTGGTTATCTATGA | 51366 |
rs375800101 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102347802 | TATTTTTAGTAGAGA[C/T]GGGTTTTCACCATAT | 51366 |
rs375816340 | snp | A/G | 3.36434e-05 | 0.00410129 | intron-variant | UBR5 | GRCh38.p7 | 8:102311895 | GCATGAACACCTTCA[A/G]AAGCACATAAATGAG | 51366 |
rs375816975 | snp | A/G | 1.68371e-05 | 0.00290143 | intron-variant | UBR5 | GRCh38.p7 | 8:102285365 | AAACTAAAATAGTTA[A/G]AACTATCCAAATAGA | 51366 |
rs375824650 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | UBR5 | GRCh38.p7 | 8:102286310 | ATGAACATGCATAAT[C/T]TAAAAAATCTATCTA | 51366 |
rs375868496 | snp | C/G | 0.000105147 | 0.00724999 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102412271 | CACTCGAGGGCGGCC[C/G]CCTCCCGCTCTCGCC | 51366 |
rs375873595 | snp | C/T | 4.63124e-05 | 0.00481186 | intron-variant | UBR5 | GRCh38.p7 | 8:102264606 | TAATTCTAGAATACA[C/T]ATATCCCCCCACACA | 51366 |
rs375888474 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102327001 | CCTCCTGGACTCAAG[A/G]GATCCTCCTGCCTCA | 51366 |
rs375895957 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102285785 | CCGCTGAACTTGCTA[C/T]AAGGAAAAAGGACAA | 51366 |
rs375935375 | in-del | -/TCTT | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B, nc-transcript-variant | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102252029 | AATGTAAAAATAGTA[-/TCTT]TCTTTATGGGAGGGA | 51366 |
rs375940323 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102297306 | ATATTTAACTGAGCA[A/G]TCAGCTCTTTTGCCT | 51366 |
rs375948758 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102270840 | ATGAAGACTTTTTAA[C/G]ATAAACTTAGGAGAG | 51366 |
rs375967647 | snp | A/G | 6.59163e-05 | 0.00574054 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102342528 | GGACTTTGAACAGGT[A/G]TATTCTTCTTATCCA | 51366 |
rs375985611 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102264628 | CCCCACACATAATAC[A/G]TATTAATATTTTGAG | 51366 |
rs375987272 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBR5 | GRCh38.p7 | 8:102286876 | ATTTGTATGCCTCAG[C/T]CTCCTGAATAAGTAA | 51366 |
rs375997827 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102343677 | ACCAAGATGGTGAAA[A/C]CCTGTCTCTACTAAA | 51366 |
rs376018307 | snp | C/T | 1.65644e-05 | 0.00287783 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102298893 | TGGAGAACCACACTG[C/T]CACATAACAATTTCA | 51366 |
rs376042422 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102360301 | ATCATTTCAGTTAAA[A/G]AGCAGATTTGACTTG | 51366 |
rs376055471 | snp | A/T | 6.71423e-05 | 0.00579367 | intron-variant | UBR5 | GRCh38.p7 | 8:102326676 | CCCCTGAAAACAAAA[A/T]ACATAAATTGGTCAA | 51366 |
rs376067830 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102283631 | GTCTTTGTGAAGCAG[C/T]GTTCCTAGGACAGGA | 51366 |
rs376070528 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102372038 | CCCCACTGCACTCCA[A/G]CCTGGACACAGAGCT | 51366 |
rs376074792 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102315378 | TAAAAAACTAGCCCT[C/T]TTTAATGAGTTATTT | 51366 |
rs376077901 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102396997 | AGGCGTGAGCCACCA[A/C]GCCCGGCCTGGTCTC | 51366 |
rs376119069 | snp | A/C | 3.31873e-05 | 0.0040734 | intron-variant | UBR5 | GRCh38.p7 | 8:102326526 | GAGGTCCCTTAAGAC[A/C]GGCTAAATCCATCAC | 51366 |
rs376141490 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102366178 | AGGTACATCCACTCA[C/T]GTTTCATGACTCTCA | 51366 |
rs376170291 | snp | C/G | 1.65868e-05 | 0.00287978 | intron-variant | UBR5 | GRCh38.p7 | 8:102270020 | CCAGTTAAGAGGTAA[C/G]TAAGTACACAGTACA | 51366 |
rs376185417 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102352526 | ATACCAGTTTGCCTA[C/T]GATAGTGCCAGTTTA | 51366 |
rs376217189 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102259751 | ACACTCAACACCATC[A/C]GTCATAAAGCTATAT | 51366 |
rs376263786 | in-del | -/A | 0.00874735 | 0.0655527 | intron-variant | UBR5 | GRCh38.p7 | 8:102402577 | CTTTTCTTAAGGCTT[-/A]AAAAAACCATCTTCC | 51366 |
rs376267357 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102272473 | CATGATTACCACTGT[C/T]GGTTTGAGGAACAAG | 51366 |
rs376268228 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102358003 | ATACAAAAATTAGGA[A/G]GGCGTGGTGGCACGC | 51366 |
rs376334604 | snp | C/T | 1.65255e-05 | 0.00287445 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102261187 | ACATTCTGTGTTCTG[C/T]GTATTTCCGCACATA | 51366 |
rs376337753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102398509 | TTCTGCAGGCTGGGC[A/G]TGGTGGCTCATGCCT | 51366 |
rs376366610 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102398697 | AAGGCAGGAGAATCA[C/T]TTGAACCCAGGAGGT | 51366 |
rs376378538 | snp | A/G | 4.96216e-05 | 0.0049808 | intron-variant | UBR5 | GRCh38.p7 | 8:102295125 | GACTTGAGGAGAAAC[A/G]AAAGACAGAATGAAC | 51366 |
rs376423416 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102387081 | GCTTCCCCAACAACA[C/T]TGTCAGGATGTTAAA | 51366 |
rs376477201 | snp | C/T | 1.66671e-05 | 0.00288674 | intron-variant | UBR5 | GRCh38.p7 | 8:102297627 | AAAGTAAGAACATAG[C/T]AGTTCATCTTTCAGG | 51366 |
rs376496968 | snp | A/G | 3.3048e-05 | 0.00406484 | intron-variant | UBR5 | GRCh38.p7 | 8:102360055 | AAGATGGTGCCTTCA[A/G]CTGGCCACAACTTAC | 51366 |
rs376506111 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102335258 | AAGCAGTGGTTACCA[C/T]GGGCTGACAAGCAGT | 51366 |
rs376523310 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102273608 | AGCAAAAAAAAACAC[A/G]AGGCCATTCATCACA | 51366 |
rs376555738 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | UBR5 | GRCh38.p7 | 8:102272823 | ATTCAATGTTGGAAA[A/G]TAGCTTGAATTTTTC | 51366 |
rs376565446 | snp | C/T | 0.000115945 | 0.00761308 | intron-variant | UBR5 | GRCh38.p7 | 8:102293952 | TCAAAAAGGATGCCT[C/T]ACTTTTTCTTTTTGG | 51366 |
rs376580855 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102390781 | ACCATGTAGTCCAAC[A/G]CAAAATATCTGCAAA | 51366 |
rs376592926 | snp | A/C/G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102317316 | CTCAGAGGGTCCTAC[A/C/G/T]CTCAGAGTCTCGCTG | 51366 |
rs376603737 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102343316 | AAAATGATTTCCTTA[C/T]CAAAATGCTTCCCAT | 51366 |
rs376651090 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102381986 | GGAAAAAGAAACATA[C/T]AGATATTTCCATTTA | 51366 |
rs376671615 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102332913 | AACTGTTGAATGAAC[A/G]AATGAATCTTAACTC | 51366 |
rs376678234 | snp | A/C | 1.65688e-05 | 0.00287821 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102279206 | TATCATTCAAAGTAG[A/C]ACCTAAACATAAAAA | 51366 |
rs376679533 | snp | C/G | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311381 | GAATGCACACCCATT[C/G]CAAGACTACTAATAG | 51366 |
rs376685115 | snp | C/T | 0.00016475 | 0.00907457 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102286461 | GCTTGGGCAGCACCA[C/T]TGGCATGGGAGCTAT | 51366 |
rs376686147 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102277645 | TCAGCCTCCCAAAGC[A/G]CTGGGATTACAGGCA | 51366 |
rs376691139 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295427 | CCTTCAGGACTGGCT[-/G]GTTTTTCGGTTACGA | 51366 |
rs376712641 | snp | C/T | 0.000165273 | 0.00908896 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102280462 | AGTTCCAAGAGTTCT[C/T]GCGTCCTTTAAAAAG | 51366 |
rs376713212 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | UBR5 | GRCh38.p7 | 8:102344930 | TGAGACTTCATCCCC[A/C]AAAAAAAAAGGCATT | 51366 |
rs376716412 | snp | A/C | 0.000722705 | 0.0189955 | intron-variant | UBR5 | GRCh38.p7 | 8:102345572 | AACAAACATCACTGC[A/C]GCATACACACAAAGA | 51366 |
rs376744744 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102314532 | CTTTTTAAAACTCTA[A/G]TTCTGAAAAACAACA | 51366 |
rs376765196 | snp | C/T | 0.000165986 | 0.00910854 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102412240 | TGGACGTCATGGTGC[C/T]TTCCTTCTCGTCCTC | 51366 |
rs376811145 | in-del | -/A/AG | 0 | 0 | intron-variant | UBR5 | GRCh38.p7 | 8:102392817 | TGAGCCTGTTATCAG[-/A/AG]GTCTCCCCACAGCTC | 51366 |
rs376843123 | snp | A/G | 0.000242185 | 0.0110015 | intron-variant | UBR5 | GRCh38.p7 | 8:102285100 | TTTTAAGTTGGGGAC[A/G]TTCTGTATATATGAA | 51366 |
rs376844363 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102354958 | ACATGGCAAAACCCT[G/T]CTCTACCAAAAATAC | 51366 |
rs376851606 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102261675 | CCACTACACTCCAGC[C/G]TGGCGACAGAGCAAG | 51366 |
rs376874836 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102398308 | CTCTGTCTCTCACCA[C/T]ACTCAGAAATCAAAC | 51366 |
rs376924723 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102254922 | TATCTTAAAAAGTTA[A/T]TTTGCATTAAGGAGC | 51366 |
rs376930819 | snp | C/T | 3.29946e-05 | 0.00406155 | intron-variant | UBR5 | GRCh38.p7 | 8:102289610 | TTATGAGTGGGCTCC[C/T]GCCACAGCTCAGATA | 51366 |
rs376940254 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102336010 | ACAAGGGTTCTCTTT[G/T]CTCTGCATCACTGTC | 51366 |
rs376945986 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102359065 | TGTAAGCCACCACAC[A/C]CAGGCCCAATTTTCA | 51366 |
rs376953968 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102253795 | AAGTGATTTCATCTC[C/T]TAAGATCTGAATGTC | 51366 |
rs376955107 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102413628 | AGGCATGTGTCACCA[C/T]GTCCGGCTAATTTTG | 51366 |
rs376955623 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102347305 | TGCTATGTCACCCAG[A/G]CTGGAGAGCACTGGT | 51366 |
rs376959482 | in-del | -/TAAAA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102371275 | CATATCCTTTTTTTT[-/TAAAA]AAAAAAAAAAAAAAA | 51366 |
rs376985734 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102287910 | TTCATAATGCGACTA[C/T]GATTATTTTAGTTTT | 51366 |
rs377031130 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102398890 | CCACCTGATAAGGGA[C/T]TAATAATGAGAATAT | 51366 |
rs377032573 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102362815 | GCATCTTTCAAAGGC[A/G]TACAGTAACTGTCTA | 51366 |
rs377037797 | snp | C/T | 0.000115516 | 0.007599 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102259103 | TGAATTTTTTGGAAG[C/T]ACATCTAGTAGACCT | 51366 |
rs377039519 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102308957 | AAAGAAAGAAAGAAA[-/T]GAAATGAAAACTCTG | 51366 |
rs377051312 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102284864 | ACACAGTGAAACCCC[A/G]TCTCTACTAAGAAAA | 51366 |
rs377100787 | snp | A/G | 1.67475e-05 | 0.00289369 | intron-variant | UBR5 | GRCh38.p7 | 8:102346217 | AGAAATGAGAAAAAC[A/G]TGACGGTGATCCACC | 51366 |
rs377166466 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102344439 | CTGCCTCAGCCTCCC[A/G]AGCAGCTGGGACTAC | 51366 |
rs377184804 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102399313 | GGAGTCTCACTCTGT[C/T]GCCCAGGCTAGAGTG | 51366 |
rs377226242 | snp | A/T | | | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102414310 | GTTTTGCTTAGGAAG[A/T]TCTTCTGAGCAAAAT | 51366 |
rs377240670 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBR5 | GRCh38.p7 | 8:102268428 | AGGCTGGTCTTGAAC[C/T]CCTGACCTCAGGCAA | 51366 |
rs377273492 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102406608 | ATAATGCATTTAGTA[C/T]TGCTTTTAGGTAACA | 51366 |
rs377284817 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102355065 | GCTGCGAAGTCAAGG[C/G]TGCAGTGGGTCAAGA | 51366 |
rs377293913 | in-del | -/ACAA | 0.103355 | 0.202472 | intron-variant | UBR5 | GRCh38.p7 | 8:102324090 | CCCATCCATTCTGCT[-/ACAA]ACAAACAAACAAACA | 51366 |
rs377308911 | snp | A/C | 4.95029e-05 | 0.00497484 | intron-variant | UBR5 | GRCh38.p7 | 8:102295384 | AACATATTGCTTCCC[A/C]CAAGTGTCATAAATG | 51366 |
rs377342987 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102337819 | TGGTATAAACACATA[C/T]ATAATTACAATTTAC | 51366 |
rs377409346 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102274460 | AGCAAGGCCAGGTGT[C/G]GTGGCTCACACCTGT | 51366 |
rs377439565 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102385527 | TCTTCCAGAATTTCT[C/T]GACTCTGTTTTTTTT | 51366 |
rs377487442 | in-del | -/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102308819 | AAATTTTAAATATAG[-/G]AAAAAGTGCTTAATA | 51366 |
rs377490023 | in-del | -/T | | | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102413469 | AACGGAAAATTATTA[-/T]TTTTTTTTTTTTTTT | 51366 |
rs377491952 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102387367 | TAGGTTTTTAAAATA[A/T]CTCTAATGTAAAAGA | 51366 |
rs377528116 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | UBR5 | GRCh38.p7 | 8:102261279 | GAAAAATTTACCAGT[A/G]CTATTTAAAGGCAAT | 51366 |
rs377530762 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102312219 | GAAACAGTCGGGAAC[C/T]TTCGGTGTTCCACCA | 51366 |
rs377575612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102403854 | CTGTTGCAAAAGCAC[C/T]GTTCTAAGCAAAAGA | 51366 |
rs377604190 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102413983 | CCAGGCATGGCTGTG[C/T]GCGCCTGTAAACCCC | 51366 |
rs377624073 | in-del | -/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102410720 | TGCTCCACTTGAGGC[-/G]GGTTAGATACACTGA | 51366 |
rs377683517 | snp | A/G | 3.30573e-05 | 0.00406541 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102275596 | TGATTCTTTTACCTC[A/G]AAACCACCCAATTCA | 51366 |
rs377689110 | snp | C/T | 3.30115e-05 | 0.00406259 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102293646 | TGGTGGTAGTGGTTC[C/T]ACTGAAAATAATTCT | 51366 |
rs377724546 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102327137 | ACTCCCAGGCTCAAG[A/C]AATCCTCTGGCCTTG | 51366 |
rs377739050 | snp | C/T | 1.65556e-05 | 0.00287707 | intron-variant | UBR5 | GRCh38.p7 | 8:102295348 | AAAATGAAAAAGAAA[C/T]AGTGACCAAAACAAA | 51366 |
rs377741782 | snp | C/T | 0.000164766 | 0.00907502 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102342557 | CAAGTTTGGCTCTCC[C/T]TCCTTGCTGGTAGAA | 51366 |
rs377747575 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102380437 | CACAGCAAAGTAAAT[A/G]GATCAGAAAATATAA | 51366 |
rs377753843 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102305944 | GCCATGTTGCCCAGG[C/T]TGGTCTCAAACTCCT | 51366 |
rs377754008 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102331859 | GTCTTCCCTCCATCT[C/T]CCTGGTACTACCATG | 51366 |
rs386360849 | in-del | -/AA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102300488 | ACATTAAAACAAAAA[-/AA]GTTTCTATCCCCCGT | 51366 |
rs386360850 | in-del | -/AAAT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102323099 | ATAATAATAATAAAT[-/AAAT]TAATTAATTAATTAA | 51366 |
rs386413506 | in-del | -/AAA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102274745 | AAAAAAAAAAAAAAA[-/AAA]AAGAAAGAAATCTAA | 51366 |
rs386413508 | in-del | -/AA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102300487 | AACATTAAAACAAAA[-/AA]AGTTTCTATCCCCCG | 51366 |
rs386413510 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102394618 | CAAAAGATCTGCAGT[-/T]TTTTTCCCAATAACA | 51366 |
rs386728333 | multinucleotide-polymorphism | AAC/GAA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102368317 | CTGTTGTGATGGCCA[AAC/GAA]AGGAACTAAAAATGT | 51366 |
rs397789651 | in-del | -/G | | | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102413159 | GTTGTATTTATGGTG[-/G]AAGTTGGTAAAATCA | 51366 |
rs397816257 | in-del | -/A | 0 | 0 | intron-variant | UBR5 | GRCh38.p7 | 8:102290370 | ATGCCTTCAAACAAA[-/A]CAGATAAGTAGTCTC | 51366 |
rs397841764 | in-del | -/TG | | | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102304360 | CTGATCTTTCACATG[-/TG]ATTTATTTCCTTATT | 51366 |
rs397891667 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102355131 | AGATCCTGTCTCTCA[-/A]AAAAAAAAAAAAAAA | 51366 |
rs397893120 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102399946 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 51366 |
rs397948841 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102365481 | CTAAAAAAAAAAAAA[-/A]CACAAAGAAAATAAC | 51366 |
rs398009104 | in-del | -/AAA | 0 | 0 | intron-variant | UBR5 | GRCh38.p7 | 8:102255435 | AAAAAAAAAAAAAAA[-/AAA]GTTAAGTATCAGGAT | 51366 |
rs398009105 | in-del | -/AAAA/AAAAT/AAAT | 0 | 0 | intron-variant | UBR5 | GRCh38.p7 | 8:102260037 | TCTTAAAAAAAAAAA[-/AAAA/AAAAT/AAAT]TATTTTTTTTTACCC | 51366 |
rs398009106 | in-del | -/ACAC | 0 | 0 | intron-variant | UBR5 | GRCh38.p7 | 8:102275361 | CACACACACACACAC[-/ACAC]GAAAAAATAAATTTG | 51366 |
rs398009107 | in-del | -/A | 0 | 0 | intron-variant | UBR5 | GRCh38.p7 | 8:102315245 | ACTGAAAAAAAAAAA[-/A]GGGTAAAGGCAAGTA | 51366 |
rs398009109 | in-del | -/A | 0 | 0 | intron-variant | UBR5 | GRCh38.p7 | 8:102325375 | AATGAAAAAAAAAAA[-/A]TACCTGCATTTAAAG | 51366 |
rs398009110 | in-del | -/T | 0 | 0 | intron-variant | UBR5 | GRCh38.p7 | 8:102326918 | TTTTTTTTTTTTTTT[-/T]GAGACGGGGCCTTTC | 51366 |
rs398009111 | in-del | -/A | 0 | 0 | intron-variant | UBR5 | GRCh38.p7 | 8:102349665 | AGCGTCAAAAAAAAA[-/A]CAAACTACTTAGGAA | 51366 |
rs398009113 | in-del | -/A | 0 | 0 | intron-variant | UBR5 | GRCh38.p7 | 8:102377719 | CTCACAAAAAAAAAA[-/A]GGTAAAATACCTACA | 51366 |
rs398009114 | in-del | -/A | 0 | 0 | intron-variant | UBR5 | GRCh38.p7 | 8:102404930 | AAAAAAAAAAAAAAA[-/A]GTTACAGCACTGAGC | 51366 |
rs398038020 | in-del | -/G | 0.5 | 0 | intron-variant | UBR5 | GRCh38.p7 | 8:102396421 | AAAGACTGTAGAGTT[-/G]GGAGTTAGGAGGCTT | 51366 |
rs398047362 | in-del | -/TG/TGTGTGTGTGTGTG | 0.5 | 0 | intron-variant | UBR5 | GRCh38.p7 | 8:102309038 | TAGATAGCTACACAA[-/TG/TGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 51366 |
rs398047363 | in-del | -/A | 0.5 | 0 | intron-variant | UBR5 | GRCh38.p7 | 8:102350475 | TTAGGGGAAAAAAAA[-/A]TAGTCTCTTCAACAA | 51366 |
rs398047364 | in-del | -/AA | 0.5 | 0 | intron-variant | UBR5 | GRCh38.p7 | 8:102400985 | AAGAAAAGAGGGTAA[-/AA]GAGCCTTTTTACTCA | 51366 |
rs398086861 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102291796 | AGAATACAAAAAAAA[-/A]AGGAAGTATCTGTCA | 51366 |
rs398096004 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102291797 | GAATACAAAAAAAAA[-/A]GGAAGTATCTGTCAA | 51366 |
rs527282608 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102324299 | AAGACTACTGTTTCC[G/T]GCTAGCCAGAAGGTT | 51366 |
rs527301889 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102279456 | TGTGTATGTTACAAT[-/A]AAAAATGCAAAATAA | 51366 |
rs527338309 | snp | C/T | 8.23703e-05 | 0.00641704 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102288188 | CATGTTGTCCCTCTG[C/T]CTCAGCATTTTCTTC | 51366 |
rs527355974 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102304820 | AATTCTCATGTAATA[A/G]GTCATCTGCAATTAT | 51366 |
rs527357185 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102383850 | AAGGGACTAAAGGAA[C/G]ACCCTAAAATATCTC | 51366 |
rs527439077 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102287277 | AAGAGTTATTAAAAT[A/C]ATACTTTCTTTTCTA | 51366 |
rs527445829 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102270786 | GGCCTCCCAAAGTGC[G/T]GGAATTACAGGCGTG | 51366 |
rs527450129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102260570 | TTGCTACAATAAACA[A/G]TAACTATTAAGTACA | 51366 |
rs527499210 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102390565 | TGTATACTGATAGAA[G/T]GTTATTTCCTCATCC | 51366 |
rs527515440 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102317503 | GTAGGCTCCACCTCT[C/G]GGGGCAGGGCACAGA | 51366 |
rs527537620 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102381380 | CTCAAACGAACAAAC[-/A]AAACCATCAGATCTC | 51366 |
rs527579324 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102274509 | GGCCAAGGCAGGTGG[A/C]TTACTTGAGGTCAGG | 51366 |
rs527586138 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102266646 | GTCCTAGGATTCTAT[A/T]CATCTTTCCCTCTCT | 51366 |
rs527609180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102325275 | AAAGTTTTCTGGTTC[A/G]AAGACCAATAGGCAG | 51366 |
rs527611853 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102317297 | GATTATATCCCTCAC[A/C]TGGCTCAGAGGGTCC | 51366 |
rs527617083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102274049 | AAATGAAACAAAAGG[C/T]CCTAATTATATAGAG | 51366 |
rs527700927 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102323066 | GCACATTGTGCACAT[A/G/T]TACCCTACAACTTAA | 51366 |
rs527701639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102383400 | ACCCAGAATCGGCGT[A/G]GGAGGGAGAAGGGGT | 51366 |
rs527703354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102264973 | AGTTCAGTCTCCCAA[A/G]GTGCTGAGATTACAG | 51366 |
rs527713362 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102359864 | TTAAAGGTCAAGAGC[C/G]TAGATTAATTGTAAT | 51366 |
rs527719776 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102316362 | TAGAAAAAAAGAAAA[A/T]ACATTGATGTGTTAA | 51366 |
rs527773667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102375298 | CCTGGGAGGCAGAGG[C/T]TGCAGTGAGCCAAGA | 51366 |
rs527777704 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102402209 | TGACAGAGTGAGACC[C/T]TGTCTCAAAAAAAAG | 51366 |
rs527784761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102374853 | ACAATCAAATATCTG[C/T]CTCCCTCACTGCCAA | 51366 |
rs527810229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102322519 | AGTTCAACCATTGTG[A/G]AAGTCAGTGTGGCGA | 51366 |
rs527812560 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102405693 | GTATGGTGGCGTGCG[C/T]CTGTACTCCCAGCTA | 51366 |
rs527822179 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102279444 | AATTTTACGTTATGT[A/G]TATGTTACAATAAAA | 51366 |
rs527834890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102390453 | CTGCACTCCAGCCTC[A/G]GCAACAGCGAGACTC | 51366 |
rs527839751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102397408 | GTTAAAGAATAAAAA[C/T]CTAGCCTGGTGCGGT | 51366 |
rs527861179 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102337914 | TGAGAAGAGAAAATG[G/T]AGCCATGTTATACAA | 51366 |
rs527866368 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102346696 | GGGGACGGAGGTTGC[A/C]GTGAGCTGAGATCAT | 51366 |
rs527867121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102294799 | CTGAGGGCACTGATA[A/G]TTTTATGTTTTCCAG | 51366 |
rs527894546 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102404119 | TGGGTTAATTTTACT[C/G]AATGTAAAGTATAAC | 51366 |
rs527906264 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102375663 | CTTTCTCCTCTCCCT[A/C]TCCCTCCCCTGCGGT | 51366 |
rs527921717 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102346097 | AAAGAAACTTTACAA[A/T]AAAATCAAGCAACTC | 51366 |
rs527926823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102354155 | TTTCCATGAAAATAT[C/T]AATTAGTCCCAACAT | 51366 |
rs527998409 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102310304 | TTGTTTCTAACCTGG[A/T]TTATTGCCTGACTTT | 51366 |
rs528004155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102403468 | GGAGGATCGCTTGAG[C/T]CCAGAAGGTCAAGGC | 51366 |
rs528007123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102257857 | GTCTAATTCCTAATA[C/T]AAGAAATTAAGAGCA | 51366 |
rs528018749 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102265538 | ACTCGGATAAGCTTC[G/T]TTCACTTTATTGCCT | 51366 |
rs528024495 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102356517 | GTAATCCCAGCACTT[C/T]GGGAGGCCGAGGCAG | 51366 |
rs528032600 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102326936 | GACGGGGCCTTTCTC[C/T]GCTGCCCAGGCTACA | 51366 |
rs528040465 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBR5 | GRCh38.p7 | 8:102259466 | GTGCTACCCTGTCAG[C/T]ATCTCAGGAAAGATA | 51366 |
rs528078640 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102300512 | CCCCCGTTTATAATC[A/G]GTAATAATTAAGTTT | 51366 |
rs528089488 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102401390 | CACTCTAGAGTTTCA[C/T]GAAACCAGAAACATT | 51366 |
rs528100925 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102301270 | TTTTTTAAAAAGTCA[C/T]TCACAAAAATTACTT | 51366 |
rs528104874 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102370029 | CCGAGAACTGCCATA[C/T]TCTAAATGCACAGTG | 51366 |
rs528126685 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102358865 | CTGCAGCCTCAACTT[C/G]CTGGGCTTAGATGAT | 51366 |
rs528152492 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102369477 | AATGTTACTATCAAT[A/C]TACAGTGTCAAACTC | 51366 |
rs528167641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102308942 | TTTTTAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA | 51366 |
rs528185928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102358019 | GGCGTGGTGGCACGC[A/G]CCTATAGTCCCAGCT | 51366 |
rs528204067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102263600 | ACTATCAAAACACAT[A/G]AAGATAAGCTAATTC | 51366 |
rs528204705 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102365575 | GTTGTAACACACAAT[C/G]AATAGGTTAGCAAAA | 51366 |
rs528214196 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102343777 | AATCACTTGAACCGG[A/G]AAGGCAGAGATTGCA | 51366 |
rs528217351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102400950 | GGCCCTATTTGCCAT[C/T]ATCAATCAATGTTAA | 51366 |
rs528224045 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102408930 | TAAATCTCTGTGCCT[A/T]TTTTTTCAGCTCATT | 51366 |
rs528245746 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102381770 | CTTTTCATTTTTTCA[A/T]ATGAGATTCAGAAAA | 51366 |
rs528247379 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102399066 | GGGCATGGAAACAGG[A/G]GTTAAAAAAAGACCA | 51366 |
rs528267902 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102286144 | TGCCTAACATCCCAC[A/C]ATGCACAAGACAGCC | 51366 |
rs528284697 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102330438 | AAATAATACTAATTT[C/T]AATCGTCTATTTTAC | 51366 |
rs528291572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102278395 | TTCTACCAAACATAG[C/T]TATAAAGATGGAGAC | 51366 |
rs528345016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102381044 | AGAGAGAAAGCAAAC[A/G]AGAACAGGGAAAACT | 51366 |
rs528351395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102345020 | TTTTCACATTTCATT[A/G]TTTTATCTAACCAGG | 51366 |
rs528362244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102336131 | CAATTACTGATGTTA[A/G]GCACCTTTTCAAATA | 51366 |
rs528422956 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102292850 | ATTGGGACACATATA[C/G]TGGCATATAGGAGAA | 51366 |
rs528433767 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102396149 | TTCTGCCCACTACTC[C/G]TAAATACCTATTAGA | 51366 |
rs528457733 | snp | A/G | 6.78806e-05 | 0.00582543 | intron-variant | UBR5 | GRCh38.p7 | 8:102327714 | ACACAAGCATTCACC[A/G]ATAAATTCCTCCTCC | 51366 |
rs528460455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102379334 | AGCAGTGTAGCCCTC[C/T]TGTTTTCTACAAAAA | 51366 |
rs528467071 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102387453 | TGGCTCATGCCTGTA[A/T]TCCCAGCACTTTGGG | 51366 |
rs528467963 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102334855 | AGGAGCCGAGATCGT[A/G]CCACTGCACTCCAGC | 51366 |
rs528473124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102284098 | TGACTTCAGGTATGA[A/G]GCACTTTTACTATAT | 51366 |
rs528480337 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102413244 | AGGGCCTTTCCAGAA[A/G]GAGATAGTAGGATCC | 51366 |
rs528485093 | in-del | -/AG | 0.00358779 | 0.0422022 | intron-variant | UBR5 | GRCh38.p7 | 8:102367858 | TTGGGGCTAACATAA[-/AG]AGTCACACCAGCCTT | 51366 |
rs528513578 | in-del | -/AAAG | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102381590 | GGCAGAAACACTGAC[-/AAAG]AACATTAATAACCTT | 51366 |
rs528520314 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102334030 | TTCCACTTTTAGAAT[A/C]CTCTGCCTTCATTTT | 51366 |
rs528520828 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102294535 | TTCTGTGTGCAGCTT[-/C]TTGTATAAATGTTAG | 51366 |
rs528542164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102291070 | TTTTCAGATTAGGAA[C/T]ACTCAACCTGTGTAA | 51366 |
rs528555039 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102370697 | ACTGTATTTTTGTAC[C/T]CGTTAACCAACCTGT | 51366 |
rs528580684 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102298554 | CTTCCTGATTATAAA[A/T]GTTCATGATAAAACA | 51366 |
rs528583959 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102386857 | GGCGGGCACCTGTAG[A/T]CCCAGCTACTCAGGA | 51366 |
rs528604567 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102335629 | TCTTGGCACACTGCA[A/G]CCACCGTCCCCCAAG | 51366 |
rs528692376 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102320187 | ACAAAATTGATAGAC[C/T]ACTAGCAAGACTAAT | 51366 |
rs528694458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102270966 | TAGTTAATAGACTAT[C/T]CTTAGTTATTGTATT | 51366 |
rs528719381 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102287763 | TTAGAAGAATGGCTA[C/G]GGAAATTATGGTAGT | 51366 |
rs528751251 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102277356 | CACCAATTCCAACGC[A/T]TTACCAAACCAACCT | 51366 |
rs528780936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102260885 | CAGTCATTTTGGTAC[C/T]ATAAGCACCCTTTCC | 51366 |
rs528783192 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102372069 | TAGCAACTATAGGCC[C/T]CCGGGTTTGACATAT | 51366 |
rs528784892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102328465 | CAATTTAGTGACTTT[A/G]AAGCCAAATCGATAA | 51366 |
rs528792565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102380038 | ATAGTCTATGACTTT[C/T]GAATCAAGAGGGAGG | 51366 |
rs528833442 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102318550 | ACTTCCCCAGTCTAG[A/C]AAGGCAGGCCAACGT | 51366 |
rs528839862 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102298670 | GTACACTACATGATG[C/T]TGAGACAGCCTCTTT | 51366 |
rs528862438 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102413290 | AGCAACTTCTATTAC[C/G]TCGGTCTCCCCAGTT | 51366 |
rs528892794 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102326896 | GGAAATTCATCAATT[A/G]CTTTTTTTTTTTTTT | 51366 |
rs528899583 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | UBR5 | GRCh38.p7 | 8:102268194 | TTGCCTCAGCCTCCC[C/G]AGCAGCTAGGATTAC | 51366 |
rs528913281 | in-del | -/A | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102351028 | ATGGCTACTATCAAG[-/A]AAAAAAAAAATTACA | 51366 |
rs528920201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102317773 | CAGACAGCAGCATTC[A/G]CGGTTCACGAAAATC | 51366 |
rs528993518 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102377916 | TTATTCCCATTAAGC[C/T]AGACTAATCAAGTGA | 51366 |
rs528996590 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102282398 | GCAAGGTCAGGCGCA[C/G]TGGCTCACACCTGTA | 51366 |
rs529039903 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102400078 | GTGATGGATCCATGG[C/T]ACCCCTCTGTACCAA | 51366 |
rs529046674 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102408089 | AGTACTAATCTAGAA[C/G]TAAGAGTCGATTCTG | 51366 |
rs529054565 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102405815 | AGCGTGGGCAAGAGC[A/G]AGACTCAAAAAACAA | 51366 |
rs529059069 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102350385 | ACGACAAAAAAGACC[A/C]ATGAAACAAAATGGA | 51366 |
rs529059920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102341581 | AATCAAAGAAAGAAA[A/G]GAAATCCATATCAGG | 51366 |
rs529060094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102393138 | AGTCCAAGTGTCTGG[C/T]CCAAAACAAGCCCTC | 51366 |
rs529076447 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102297913 | CTATTTAGCAAATTA[C/T]AGACCATCTCATAAA | 51366 |
rs529080188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102306710 | CATATACACTGGTTT[C/T]AAGTAACAGCAAATT | 51366 |
rs529107860 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102399479 | ACAGGGTTTCGCCAC[A/G]TTGGCCGTGCTGGTC | 51366 |
rs529111371 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102254138 | GCTAGTGCTCCTTAG[C/G]CCTTTAAGCTATAAA | 51366 |
rs529129459 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102349580 | GCAAAGGGGGAAAGA[A/G]GACAGGAAGGGAGAG | 51366 |
rs529144747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102357162 | TGATGCACTGAAAAG[A/G]GCACATCATCACTTC | 51366 |
rs529222032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102406678 | TAATATGATGCTCCA[C/T]CCCACACAACCTAAT | 51366 |
rs529223917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, nc-transcript-variant | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102252057 | GGATGTTGTTTGGGG[A/G]CAGCTACTAAATAGT | 51366 |
rs529226923 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102373732 | ACAATCGGGGTTATA[C/T]TCCTGATCGAGGATC | 51366 |
rs529249215 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102398034 | TTATCCTGAGCAAAA[C/T]AACAAAATTGGAGGA | 51366 |
rs529262842 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102266504 | CTTGTTTTTGCAATG[G/T]TGGCACCAGCTACTT | 51366 |
rs529264247 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102347740 | GCCTCTGCCTCCTGC[A/G]TAGCTGGGATTACAG | 51366 |
rs529298745 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102304601 | TATCATCAGCAAATT[A/C]AAAAAAAAAAACACA | 51366 |
rs529308159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102405292 | ACTGTGTGATGGGAA[C/T]ATGGTTGTTCATCAT | 51366 |
rs529324966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102354439 | TTAGCTCAGATTAAA[C/T]CCTAAAGGAATATGG | 51366 |
rs529352031 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102292067 | TTATTTATTAAGAAC[A/G]TAACAAGAACATTTT | 51366 |
rs529357278 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102267367 | AGCAAATTCTCTAGC[G/T]AATTTAATGATTCTA | 51366 |
rs529365583 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102369662 | CATTATTTGTCAGTC[A/T]GTCTCAAATAAAAAT | 51366 |
rs529365647 | snp | A/C | 6.67067e-05 | 0.00577485 | intron-variant | UBR5 | GRCh38.p7 | 8:102361089 | CTATTTTAACAGTTT[A/C]TTTTTCATTTCTGTA | 51366 |
rs529383521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102317473 | ACCACAGCTCAAGGA[A/G]GCCAGCCTGCCTCTG | 51366 |
rs529388846 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102264024 | AGGCATAAGCCACCG[G/T]GCCTGGCCTGGAAGG | 51366 |
rs529404019 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102404422 | TAATTTCTTATAGCC[A/C]AGTTCAATTGACTAA | 51366 |
rs529416013 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102266562 | AGAACTCCTGATCTC[C/G]TGATCTGCCCACCTC | 51366 |
rs529420241 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102310820 | AGGTAGCGTTAGGTG[A/T]ACACACAAACACCCT | 51366 |
rs529428941 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UBR5 | GRCh38.p7 | 8:102281978 | AAACACAGATATCCT[A/G]GGCAACATGGTGAAA | 51366 |
rs529439861 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102412149 | CCCCTCCCCCCGCGC[A/C]CGCCGACCCGCCAGC | 51366 |
rs529447322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102289635 | CAGATATGCAACACA[C/T]ATTTTTATTTAACTC | 51366 |
rs529478350 | in-del | -/ATT | | | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102413462 | GAATCAGAACGGAAA[-/ATT]ATTATTTTTTTTTTT | 51366 |
rs529512017 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102340279 | CATTCAAACTGTCTT[A/G]AGCTAGGAATTCCTA | 51366 |
rs529525767 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102348175 | GAGGTAGCAGCGAGC[C/T]GAGATCGCGCCACTG | 51366 |
rs529530707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102392007 | AAATACCATGGCAAC[A/G]TCAGGAAGTTACCCT | 51366 |
rs529559272 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102288819 | TTTACCTCATAAATA[C/T]GTAGTATCCTCTTTC | 51366 |
rs529576947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102339564 | AATTTTGAAGAACTG[A/G]TTGTTCCTCTAAATG | 51366 |
rs529592549 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102296559 | CCTAGTATACCCCAC[C/T]ACAGGGGACCTGAGA | 51366 |
rs529598027 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102344757 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 51366 |
rs529601366 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102399080 | GAGTTAAAAAAAGAC[C/T]AAATGATCTAGCCCA | 51366 |
rs529603873 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102323284 | GAACTGGTGTCAAAG[C/T]ACGATTAGTTAAGCT | 51366 |
rs529608725 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102398637 | AATACAAAAATTAGC[C/T]GGGCATGGTGGTGGG | 51366 |
rs529629776 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102383047 | GAAAGACGAGGCTAG[C/T]GCATTCAACAAATTT | 51366 |
rs529644177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102331602 | TCCTAACATGGTAAA[A/G]TGAATTACTGCCTGG | 51366 |
rs529684839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102390835 | GGTACAAGACTTCAT[A/G]AGGTCTAGGGAAAGC | 51366 |
rs529690600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102287034 | AAAAAAAATTAGCCC[A/G]ATGTGGTGGCTTGCA | 51366 |
rs529732389 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102350928 | ATATAAATGGCCAAC[A/C]AGCAAATGAAAAGAT | 51366 |
rs529753162 | snp | C/T | 1.68238e-05 | 0.00290028 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102293719 | AATGGTGCAGTTGGA[C/T]GAGCAATCCCCATTC | 51366 |
rs529754925 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102252360 | TATTAGAAGTATTTT[C/T]TAACCAAAATCTTGA | 51366 |
rs529755616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102345953 | GTAGTCCCAGCTACT[C/T]GGGAAGCTGAGGCAG | 51366 |
rs529797123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102390215 | AAAGCCAATCCTTAC[A/G]TAGCATCAAGAAGCA | 51366 |
rs529800874 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102282395 | TGGGCAAGGTCAGGC[A/G]CAGTGGCTCACACCT | 51366 |
rs529817208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102353427 | AAACTTAAAGCCCAT[A/G]GGCCAAGTCTTGTCC | 51366 |
rs529847741 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102317246 | CCACCTGAATACTGC[A/G]CTTTTCTGACGGGCT | 51366 |
rs529859519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102396826 | TTCTCCTGCCTCAGC[C/T]TCCCAAGTAGCTGGG | 51366 |
rs529867223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102369018 | AAAAATAAACTAACT[A/G]AATATTGACATAAAT | 51366 |
rs529900920 | in-del | -/T | 0.00755907 | 0.0610114 | intron-variant | UBR5 | GRCh38.p7 | 8:102366980 | GAAAAAGAAATACTG[-/T]TAAGAATATTTCTGG | 51366 |
rs529910550 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102411531 | TAATAATAATAACAA[A/T]AATCATGGCGCTTCC | 51366 |
rs529913416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102332221 | TCCTCTCAGATTCTT[C/T]TCTTTCTCTCTCCCC | 51366 |
rs529921198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102323165 | TTAGCACTTCCTTTC[A/G]AATTTCCTGGGAACC | 51366 |
rs529945932 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102267268 | GAATGTGGTCTTCAT[-/A]GGGGTGCTGGAACAC | 51366 |
rs529949305 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102375385 | AAAATAAAATGAATA[A/C]AAAATAAAAGTGATT | 51366 |
rs529970885 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102363343 | TTTTCATTAGTTCAA[C/G]AAAGTTAAGCTTTTT | 51366 |
rs529989567 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102315679 | ATCTCAATAAGTACA[A/C]AGCAAATACTCCTGG | 51366 |
rs530009316 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102383811 | ACCTACATCAAGGTA[C/T]ATCAGTGTGAAATTT | 51366 |
rs530051611 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102321354 | TTGCTTCAAAGAGAA[A/T]AAAATACTTAGGAAT | 51366 |
rs530055972 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102280109 | AAATGTAATAAGAGT[A/T]TATTAAGAGTAAAGG | 51366 |
rs530103259 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102322410 | ATCTCACACCAGTTA[G/T]AACAGCGATCATTAA | 51366 |
rs530122062 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102279364 | CATAGTCCAAAATTC[C/T]GGTATTTTTTAAAGT | 51366 |
rs530123158 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102407233 | CTCACAGGCACAAGC[A/G]ATTCTCCTGCCTCAA | 51366 |
rs530138518 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102374735 | ACAAACTGTGGGAAA[C/T]CTTAATTTACCCTTC | 51366 |
rs530141574 | in-del | -/CCAACGCATTACCAAA | 0.00953873 | 0.0683987 | intron-variant | UBR5 | GRCh38.p7 | 8:102277349 | GGCTGACCACCAATT[-/CCAACGCATTACCAAA]CCAACCTCAGATAAC | 51366 |
rs530141717 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102332275 | CTCACAATTTCCTTG[-/A]ACAACTGTAGCATTC | 51366 |
rs530148975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102365945 | GGTTCTTCGGTTTCA[C/T]AATTCTCTGCCTAAC | 51366 |
rs530173136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102285441 | AACATTTAATTCCCC[C/T]AATACTGGAATTCTC | 51366 |
rs530185032 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102253261 | GTCAAAATTTTTATG[C/T]ACATAACCATGTCAG | 51366 |
rs530205589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102381617 | TAACCTTTCTCTAAC[A/G]AATATACAGAAACCT | 51366 |
rs530240526 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102355111 | CCAGCCTGGGCAACA[A/G]AGGGAGATCCTGTCT | 51366 |
rs530265044 | in-del | -/ATTA | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102310175 | CAAATCAGAAGCTTT[-/ATTA]ATTCTTTCATTCACT | 51366 |
rs530270009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102403096 | TTCCTATGAAAAACA[C/T]TGTGATAAATTGAAG | 51366 |
rs530271002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102352863 | CTCAAATTCTTTTCT[A/G]TAAGCACTGCTGATT | 51366 |
rs530278501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102396453 | CAGTTCTCAGAGCTG[C/T]CTTCCATAGGGCCTG | 51366 |
rs530290934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102258875 | AATGCTTGAGTAATA[C/T]AGCAATTTCCCAAAC | 51366 |
rs530336175 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102410493 | TTTAATGAAGTAAAG[G/T]CAGGCTAAGAACCAC | 51366 |
rs530343113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102316252 | TATAATCATAACATC[C/T]GAGTATAAATGGAAA | 51366 |
rs530358635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102409709 | TGAAAATACGCTTAT[C/T]CTAGTTAATTAAAAG | 51366 |
rs530360075 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102360279 | TAATTTGGAAATGAT[A/C]TATAAAATCATTTCA | 51366 |
rs530383638 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102400901 | AGTCTAAGGGGAAAA[C/G]GAAGGTTGGAGGCAG | 51366 |
rs530406068 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102264787 | CTCTGTCAACCCAGG[A/C]TGAAGTGCAGTGCCA | 51366 |
rs530414461 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102373446 | CCGACCAAAATTTCA[A/G]GAGAATATACTAGGC | 51366 |
rs530425711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102255218 | AACATTCCTCATCAA[C/T]CCATCCCTTCATACA | 51366 |
rs530435172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102366698 | AACTGCCTATAAAGT[A/G]ACCCCACCTCACCCC | 51366 |
rs530436008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102263472 | AATATTTTTAGGAAC[A/G]TGGGTAGTTTTCTTT | 51366 |
rs530443475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102264260 | TACTCTGCTATGCCA[C/T]CTCCCCATAGTCTTT | 51366 |
rs530449344 | snp | A/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102272538 | ACTTACTTGTGTGGG[A/T]GCCTTTGTTGGCATT | 51366 |
rs530457026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102357867 | TAAATAAGAGTAGGC[C/T]GGGTGCGGTGGCTCA | 51366 |
rs530515205 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102300695 | TTTTTAACAGTACAA[C/T]TTGCATCCCAAAGAA | 51366 |
rs530516368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102365094 | CACACTGAAGCTCAC[C/T]AAATTCCATTTCAGA | 51366 |
rs530526506 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102373016 | TTTGTTTTTGTTTTT[C/G]CTTTTTGTGGAGAAC | 51366 |
rs530550904 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102344129 | GTCCAGTTTAAAGAT[C/G]AGTAAATACAGCCAA | 51366 |
rs530555964 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102371677 | CACTGCAACCTCTGC[A/G]TCCCTGGTTCAAGCG | 51366 |
rs530557329 | snp | C/T | 3.30475e-05 | 0.00406481 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102270058 | TGCATTGCTTGTACA[C/T]GAGGATAAAGCCTCT | 51366 |
rs530594950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102284853 | CACCATGGCTAACAC[A/G]GTGAAACCCCGTCTC | 51366 |
rs530625794 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102357300 | CAGAAAGATAAAGAC[C/T]GAGGATCTGGCCCAG | 51366 |
rs530628529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102270889 | ATTCAAATAGGAACT[C/T]GAGTCAGATAAAAAG | 51366 |
rs530639124 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102314053 | TTTCCTAAGCTACTG[A/C]TTTATGAATTGGAGT | 51366 |
rs530658910 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102397420 | AAATCTAGCCTGGTG[C/T]GGTGGCTCACGCCCG | 51366 |
rs530677040 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102346849 | ACCCACCATATTCAG[C/T]AAAACCTCACCTTGT | 51366 |
rs530698435 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102395382 | TTTTAATGATTTCAC[A/T]TATATCTATTTATAT | 51366 |
rs530711421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102336052 | TCTCTTGTCTTTTTG[A/G]TAACAACCATCCTAA | 51366 |
rs530757860 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102394501 | TTGTTTTAGCACTTA[A/T]GAAACTTTAGTCTTT | 51366 |
rs530759741 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102319117 | TAAATGGACTAAATG[C/T]TCCAATTAAAAGACA | 51366 |
rs530785973 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102343775 | AGAATCACTTGAACC[A/G]GGAAGGCAGAGATTG | 51366 |
rs530790988 | snp | A/G | | | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102313897 | CTCTTCTTTTGGTGC[A/G]GGGGTTGACCGTCGT | 51366 |
rs530801139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102342213 | TTATCTAGAACTAAC[A/G]TCCTAATTTCTCTGA | 51366 |
rs530867425 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102309193 | CCTCTTAAGTAGCTG[C/G]GATTACAGGCACAAC | 51366 |
rs530871501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102349244 | ACAATCCAGGCTGGG[C/T]GTGGTAGCCCACACC | 51366 |
rs530886731 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102254036 | CAAAAAGATAAATCA[C/G]AGTGTAAATTATGTT | 51366 |
rs530898183 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102393611 | ACTGCACCCCAGTCA[C/G]GGGGACAGAGCAAAG | 51366 |
rs530905712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102386298 | AGCTGGGTGTGGTGA[C/T]GCACGCCTGTAATCC | 51366 |
rs530912604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102306569 | TTAATACTAAACTTT[C/T]CAAAACATAGGGAAA | 51366 |
rs530920424 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102334427 | CTCCCACGTAGCTGG[A/G]ACTACAGGTGCACGC | 51366 |
rs530935596 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102348402 | GATAGTACTGCATTA[A/C]TATTCAGCACTATCA | 51366 |
rs530978580 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102371841 | ATCTGTCTGCCTCGG[A/C]CTCCCAAAGTGCTGG | 51366 |
rs530987590 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102337466 | CTAAACTGTTAAAGA[A/G]TTTTTATCAAGAAAG | 51366 |
rs531009746 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102393090 | GTGAACTCCACAGGG[C/G]CAGACATTTTTGCCT | 51366 |
rs531034913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102276649 | ATCTTATTTTCAAAC[C/T]AGCTTTTTAACTCCC | 51366 |
rs531037940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102297168 | ATACAAATAGAAATA[C/T]TACCAGTAGAAAAAA | 51366 |
rs531072871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102399344 | CAATGGCGCGATCTC[A/G]GCTTACTGCAACCTC | 51366 |
rs531079730 | snp | C/T | | | intron-variant, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102258919 | CTTAAGAACTAGAAA[C/T]TCAGAAAATGCTGAC | 51366 |
rs531118088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102386822 | CTCTACTAAAAATAC[A/G]AAAATTAGCCTGGTG | 51366 |
rs531123786 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102290410 | TTTAACACTAGAACT[A/G]TAAGTAACTGGTAAA | 51366 |
rs531124952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102319133 | TCCAATTAAAAGACA[C/T]AGACTGGCAAATTGG | 51366 |
rs531139335 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102306890 | TGTCAGTTATTCTTA[C/T]AGCAAAAGGCAGAGT | 51366 |
rs531150121 | snp | C/T | 1.65362e-05 | 0.00287538 | intron-variant | UBR5 | GRCh38.p7 | 8:102360224 | TAAATTTTTGAAGAC[C/T]AACATTTTTTACAAC | 51366 |
rs531185647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102276261 | TATGGCTTCTTCACC[A/G]CAATGACAGTTCTCC | 51366 |
rs531208383 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102412418 | CGCGGCCCGGAGGGG[A/C]GGGCAGGAGGGCGAA | 51366 |
rs531230503 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102282308 | TCCCAAATTATATAC[C/T]TGATAATGGGCTTAC | 51366 |
rs531242210 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102261680 | ACACTCCAGCCTGGC[A/G]ACAGAGCAAGACTCC | 51366 |
rs531272353 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102290898 | TTTGATCTTGGGTTT[G/T]TTTTTTTTTTTTTAA | 51366 |
rs531302397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102369920 | TTAAACCACAGCACA[A/G]ATGTCAAAATGGTGA | 51366 |
rs531344949 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102325444 | AAACTACCATTTTGT[C/G]TAAGTTTTAAGGATT | 51366 |
rs531350536 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102302851 | CTTTCATCTGTTCAA[C/T]CGGCAGCCCTGAGTT | 51366 |
rs531361666 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102274560 | AACATGGTGAAACCC[C/T]GTCTCTATTAAAAAT | 51366 |
rs531377025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102407494 | TTGCGGCCAGGTACA[C/T]TGGCTCATGCCTGTA | 51366 |
rs531419521 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102381083 | AACCAATCAGCTCTC[A/G]ACCAGGCATGGTGGC | 51366 |
rs531432766 | snp | A/C | | | intron-variant, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102276830 | AAGTGTGAATCACAA[A/C]TCTAGAAAGTTCTAC | 51366 |
rs531432944 | snp | C/T | 6.59239e-05 | 0.00574087 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102312415 | TCTGGACCAGAGCTG[C/T]TCTGACAGTTAGTAT | 51366 |
rs531439866 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102363527 | TAACAGCAGCCTTTA[G/T]AAGACCCCAAGAAGC | 51366 |
rs531498805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102261781 | ATCTTTAACACCGAC[A/G]GTATCCATCTCTCCT | 51366 |
rs531519434 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102317751 | ACAAAACTTCCAGAG[C/G]AACGATCAGACAGCA | 51366 |
rs531524575 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102306106 | AATTTAATTAACAAA[C/G]ACACAGTGGTACTGA | 51366 |
rs531536125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102261390 | CAGAATCTAAGAGAT[A/G]GAAACATTTTAGGCC | 51366 |
rs531541900 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102409572 | TTTTCATACATAACT[A/G]TGATTATCATTTTAT | 51366 |
rs531544454 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102275255 | ACAAAAAAATTCATA[A/G]AGGATGCTAGGGAAC | 51366 |
rs531556991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102405990 | TCCTAAATAACCTAA[C/T]GGTCTAATTGTTAGG | 51366 |
rs531600320 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303506 | CAAGCAGACAATAAA[G/T]TTTTTTCCTACAGAA | 51366 |
rs531612437 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102259198 | ATTATTAAAGCACAA[A/G/T]ACATAATTTTAGCAG | 51366 |
rs531617770 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102403531 | AGCCTGGGCAATAGC[A/G]CAAGAGCCTGTCTCA | 51366 |
rs531635856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102268072 | TTATTTATTTATTTA[C/T]TTATTTATTTTTTGA | 51366 |
rs531644075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102370454 | TTTAACTGATAGATA[C/T]ATTTATGGGGTGCAT | 51366 |
rs531673349 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102267544 | TTCTTGATTTTTCTA[A/T]AATGGACTAAGCTAT | 51366 |
rs531700716 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102368263 | ACAGTTGACCACAGG[A/C]AACTTAAGAGTTTAA | 51366 |
rs531709771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102273934 | GAATGGACTTATATC[C/T]ATTCTTTTGTAGAGT | 51366 |
rs531711113 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102399186 | AAAGAACAAATTCAC[A/G]ATCCTGCTTACTCCA | 51366 |
rs531724915 | snp | C/T | 0 | 0 | intron-variant | UBR5 | GRCh38.p7 | 8:102310750 | AAAAAATCAAAAGCA[C/T]GTCATTCACTGGCTT | 51366 |
rs531746704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102410811 | ACAAACAGGGCATCA[C/T]GCAACTTAAGTCACC | 51366 |
rs531767529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102384020 | CCAACCAGAAATCAT[A/G]TATCTAGCCAATACA | 51366 |
rs531770730 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102353707 | TTGGAAACTAGACAT[G/T]GGGTACATGGGAACT | 51366 |
rs531804009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102397998 | TTATATGGAACCACA[A/G]AAGACCCAAAATAGC | 51366 |
rs531828406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102390939 | AAGACAATGAATATC[A/G]AGGCTGGGTGTGGTG | 51366 |
rs531889493 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102391473 | AGTGGCTATATAGAA[A/G]AAGGTTCATACTTAG | 51366 |
rs531923614 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102339532 | GAAACTCCATCACAA[A/C]AAAAAAAAAAAGGTA | 51366 |
rs531928290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102397430 | TGGTGCGGTGGCTCA[C/T]GCCCGTAATCCCAGT | 51366 |
rs531934192 | in-del | -/AAAAC | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102350189 | CAAAACCCTGTCTTA[-/AAAAC]AAAACAAAACAAAAA | 51366 |
rs531956274 | snp | C/T | 9.15089e-05 | 0.00676358 | intron-variant | UBR5 | GRCh38.p7 | 8:102323273 | GAGCAAACAAGGAAC[C/T]GGTGTCAAAGCACGA | 51366 |
rs531960826 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102334269 | TAGACTAGATAGAAA[A/T]AGATCCAGAACAGTA | 51366 |
rs531967950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102389423 | ACCCCAGTTGTTTTG[A/G]GTCTTTAAATGAAGA | 51366 |
rs531987120 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102347716 | CGATCTCGGCTCACT[A/G]CAACCTCCGCCTCTG | 51366 |
rs531987202 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102338604 | TTCCTGGGACAGGAC[A/C]ATGCTTCTCCTTGCT | 51366 |
rs531998207 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102346792 | TAGGATCAAAATAGG[A/C]AAACAGTTGTTTCAG | 51366 |
rs532037112 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102304434 | TAATAAGAAGACTGA[A/T]ATTTAGCTTTCACTT | 51366 |
rs532040782 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102352621 | TATGGCCATCACAGA[A/T]TAAAGGGAAGACTCC | 51366 |
rs532078354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102382646 | TGCACTTTGATAAGT[C/T]AGTTAAATGTGCATA | 51366 |
rs532114453 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102391071 | CTACTTCAGAGGCCA[A/G]AGTGGGAGAATCTCT | 51366 |
rs532128681 | snp | C/T | 3.36814e-05 | 0.0041036 | intron-variant | UBR5 | GRCh38.p7 | 8:102293594 | GAATCTGTTACCTGG[C/T]AGCAATTTACCTGCT | 51366 |
rs532146213 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102375372 | GTCTCAAAAAATAAA[A/C]ATAAAATGAATAAAA | 51366 |
rs532161416 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102396224 | AGAATCAAACCTTAA[A/C]ATGGCAGAACTGGCC | 51366 |
rs532195560 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102309984 | TCCTTTTAAAATGTT[C/T]ACTGATATCAGGTCA | 51366 |
rs532195907 | in-del | -/AA/AAAA/AAAAA | 0.180523 | 0.254677 | intron-variant | UBR5 | GRCh38.p7 | 8:102260026 | GCAAGACACTGTCTT[-/AA/AAAA/AAAAA]AAAAAAAAAAATATT | 51366 |
rs532198761 | in-del | -/T | 0.00032166 | 0.0126778 | intron-variant | UBR5 | GRCh38.p7 | 8:102279235 | AGATAAAATGTTTTG[-/T]TTTTTTAGGAAAATT | 51366 |
rs532217575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102301983 | TATTCTCCAACTTCT[A/G]GCTTAAAGCAGATTA | 51366 |
rs532217585 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102255401 | GGAAAGCTCATCTAG[A/C/T]ATTCTATATAAAGGG | 51366 |
rs532239900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102309597 | CTTTAGACCGTATTT[C/T]TACTGTGCCTTTCCT | 51366 |
rs532252199 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102257831 | ACATTATTTAAGACT[C/T]GGGGGGGAGCGTCTA | 51366 |
rs532252621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102300745 | GTTTATAAAATGTGT[C/T]GTTAATGTATGGGCA | 51366 |
rs532257534 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102374936 | CTGACACATAGTAAA[C/T]GCTTATTTATATGGA | 51366 |
rs532262199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102395390 | ATTTCACATATATCT[A/G]TTTATATATATACAC | 51366 |
rs532269224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102279509 | TGCCATTTTGTATTG[A/G]ACAAAGGTTTCCCAT | 51366 |
rs532275375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102402298 | ATTGCTGATGCTTCC[C/T]TAAAAGACTTAAAGC | 51366 |
rs532336742 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102337670 | TTGAATTCAGTTTCC[C/T]GAATTTTTTTTGGAG | 51366 |
rs532342238 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102323100 | ATAATAATAATAAAT[A/T]AATTAATTAATTAAT | 51366 |
rs532350289 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102286348 | TTAGCAATACTAAGT[A/T]TTCAGACTTGCCTGC | 51366 |
rs532360790 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102280039 | GGTAATTCTCATTTT[C/G]TTGATTAAATCTATT | 51366 |
rs532364666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102329554 | CCTACAAGGTATCCA[A/G]TTAAGGTGGCCCTGG | 51366 |
rs532367862 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102340535 | ACCAGTTTCTTCACA[A/T]GGTATTTATCCTGCG | 51366 |
rs532398943 | in-del | -/GAGAA | 0.0146672 | 0.084371 | intron-variant | UBR5 | GRCh38.p7 | 8:102318370 | TGAATGAAATGAAGC[-/GAGAA]GAGAAGTTTAGAGAA | 51366 |
rs532409645 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102286931 | TGCCTATAATCCCAA[A/C]AACTGAGGAGGCTGA | 51366 |
rs532414635 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102382777 | ACCACAGATACATGA[C/G]CAGAGATTATGAGAA | 51366 |
rs532424640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102277481 | TCTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 51366 |
rs532424884 | in-del | -/A | 0.00557542 | 0.0525036 | intron-variant | UBR5 | GRCh38.p7 | 8:102333558 | CATGAAATAGCGGCC[-/A]AAGCTTTAAAAAACA | 51366 |
rs532442377 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102365600 | GCAAAAAGCTTCTGA[C/T]AATCCTTGGGTACTC | 51366 |
rs532468136 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102388239 | AGATGTGTCTTCTTC[A/G]TATTAATCATACTGG | 51366 |
rs532482391 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102369722 | AAACGATCTTATGCT[A/C]AAAGGTATAGATTTA | 51366 |
rs532513749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102380800 | ATCCTTCCACCTCAG[C/T]CTCCCAAGTAGCTGG | 51366 |
rs532524789 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBR5 | GRCh38.p7 | 8:102284993 | AGTGAGCCGAGACGG[C/T]ACCACTGCACTCCAG | 51366 |
rs532525785 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102256697 | CCCATCTCACCATAG[A/C]AGAGAAATATTAGAA | 51366 |
rs532538843 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102387506 | TGAGCCCACGAGTTC[A/G]AGATCAGTCTGGGCA | 51366 |
rs532562836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102256857 | CACAAATAACCACTT[C/T]CCCTTATTCAAATAA | 51366 |
rs532585587 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102370074 | AATACTAAATCGACA[-/T]TGGGGGGAAAATGAG | 51366 |
rs532591441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102309027 | AAGTTATTTTTTAGA[C/T]AGCTACACAATGTGT | 51366 |
rs532630511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102380123 | AAGAGGCCGGGCGCG[A/G]TGGCTCAGGCCTGTA | 51366 |
rs532632984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102359036 | TCACCTTGGCCTCCC[A/G]ACGTGCTGAGAGGTG | 51366 |
rs532693232 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102365757 | CAGCAAACTGATGTT[A/T]ATTAACAGAGACAGG | 51366 |
rs532697906 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102321186 | TTGTATATCTAGAAA[A/G]CCCCATCATCTCAGC | 51366 |
rs532729635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102409641 | AGCTACAGTAGCAGT[A/G]GCTTTTTTATTGCCC | 51366 |
rs532733496 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBR5 | GRCh38.p7 | 8:102282589 | AGAATCACTTGAGCC[C/T]GGGAGGCAGAGGTTG | 51366 |
rs532756260 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102409006 | TCCCCTCAAGCTCGA[C/G]GAACCACATTCTTTA | 51366 |
rs532759877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102262609 | TCTAGTTCTTTAAAT[A/G]AGAACATTTTAGCTG | 51366 |
rs532762733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102264187 | GGCAGAAATGTCAGC[A/G]TATTTGTTTGCAACA | 51366 |
rs532767848 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102406778 | AGCTTTCAACTATTA[A/T]AACCTCTACTCACCA | 51366 |
rs532772258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102269862 | AAGCTATACAGTTAC[C/T]CTTCAGTAAACACTG | 51366 |
rs532786013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102313989 | ATTTCATCTAAATTT[A/G]TAAGAAAGACTATCT | 51366 |
rs532801358 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102335498 | TAAATACATGTATCC[A/T]ATAACCTGTTGTAAA | 51366 |
rs532816226 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102392869 | CAAACTGAAGGAAGG[-/C]CAAGTTTAAAGAGTA | 51366 |
rs532858811 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102374369 | TGGAAAAAGAAATCT[C/G]TGAACACACTGTAAC | 51366 |
rs532859191 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102268871 | AATAAAAATGCATTT[A/C]AAGTCTTATACTTTA | 51366 |
rs532859539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102314999 | ATTAATTTTTTCATT[A/G]TATATTTTTAAGACT | 51366 |
rs532872537 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102278009 | CTCAAAAAATAAAAT[A/T]AAATAAATAAATAAA | 51366 |
rs532884267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102371745 | AGGCACCTACGACCA[C/T]GCCTGACTAATTCTT | 51366 |
rs532897769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102276192 | CTCCATTTGTTAAAT[A/G]AATATGTCCACGTCA | 51366 |
rs532897825 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102347149 | CATTCTGATTGCTTG[C/G]TTTTCATTATTATTA | 51366 |
rs532901289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102280073 | CATCAATATTAACAA[C/T]GGTTTTGCTAAGATT | 51366 |
rs532907099 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102254203 | GGTACCACCAGGGGG[A/G]TATGACAGCATTAAC | 51366 |
rs532938348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102306747 | TTAGAAGCAGCTACT[A/G]CTCTACAGGAAACTC | 51366 |
rs532938769 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | UBR5 | GRCh38.p7 | 8:102394363 | CCGCATCCGGCCAGA[A/T]TTTATTCTTTTTCTA | 51366 |
rs532943405 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102299386 | GTAGATCTGTAGAAC[A/C]CTATATCCAAAGTGT | 51366 |
rs532963827 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102319445 | CATAAAGCAAGTCCT[C/G]AGTGACCTACAAAGA | 51366 |
rs532974442 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102319101 | ATATTAACTTTAAAT[A/G]TAAATGGACTAAATG | 51366 |
rs532977716 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102400794 | AAAAAAAGAAGCGAA[A/C]AAAAATAAACTACTC | 51366 |
rs532994745 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102356635 | CATGTTGGTGAGCAC[C/T]TGTAGTCCCAGCTAC | 51366 |
rs533009870 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102414233 | TTCGAAGGCAAAAAC[G/T]GAGAACATGACATTC | 51366 |
rs533019178 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102404801 | AATCTCAGCCACTTG[A/G]GAAGCTGAGGCAGGA | 51366 |
rs533043563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102363787 | AAATGTTGTTTCCAC[A/G]TCTCCAAATATTCCA | 51366 |
rs533057276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102371388 | TAGCTGAGACTATGG[A/G]CGCATTCCACCATGG | 51366 |
rs533058313 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102255071 | GCAATAAGCCATATT[A/C]ACACTAAGTTTTATC | 51366 |
rs533079442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102318608 | ACAAAGATACTCCTC[A/G]AGAAGAGCAACTCCA | 51366 |
rs533081626 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102379561 | CTCCACCAACCCTGA[C/T]TGTCGACAGTCAGTG | 51366 |
rs533085032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102307446 | AAGCTAAGAATGAGT[C/T]TGGGTGTCTAAATAA | 51366 |
rs533134323 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102334931 | AATAAATAAAATAAA[A/T]AAATAAAAAGTATCT | 51366 |
rs533135071 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102333137 | ACAAATGAAGATGAA[C/T]AGCACAACTATGAAC | 51366 |
rs533148336 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102269289 | GAAACTTGGCAGGGA[A/G]TAAACAGTCCATGCA | 51366 |
rs533170227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102393861 | CTTGAACCAGGGAGA[C/T]GGTGGTTGCAGTGAG | 51366 |
rs533180858 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102252942 | TTTTAAGTCACTTCA[C/T]TGAAGACTTAAGGAA | 51366 |
rs533195197 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102348213 | GCCTGGGCAACAGAG[C/T]GAGACTCTGTCTCAA | 51366 |
rs533213537 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102347849 | GAACTCCCAACCTCA[A/G]GTGATCCACCCACCG | 51366 |
rs533214231 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102296333 | AGTCCAATTCTCTAT[G/T]ATAACATTTGTAGCC | 51366 |
rs533223346 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | UBR5 | GRCh38.p7 | 8:102350467 | AAGACCACTTAGGGG[A/G]AAAAAAAATAGTCTC | 51366 |
rs533280259 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102362760 | TAGGAGTCAGCTGTT[C/G]TATAACTTTATCCTA | 51366 |
rs533295897 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102398112 | AAAAGCATGGTACTG[G/T]CATAAAAACAGACAC | 51366 |
rs533300849 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102289114 | AGGTTGCAGTGAGCC[A/G]AGATCACGCCACTGC | 51366 |
rs533350759 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102337880 | TTCTAATCTAGAAAA[A/C]ATAAATTGCAAAAAT | 51366 |
rs533424468 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102386061 | CACCCTAGCATGTAA[C/G]GATGGAGAAGCAAGA | 51366 |
rs533426118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102341264 | AAAAGTAAAAGCCCA[A/G]TGGTTTAAATCAGTC | 51366 |
rs533445765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, nc-transcript-variant | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102252170 | GGAAAAAAATAGTAG[C/T]AGCAAACTCTGAAAA | 51366 |
rs533472755 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102305367 | ATATATTAAAAATTT[C/G]TCATGGCCAACACAA | 51366 |
rs533484136 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102385636 | CAGCCTCAAACTCTC[A/C]AACTCCTGGGTTCCA | 51366 |
rs533493263 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102392993 | TACAATTTTTAATAA[G/T]ACATTTCAAATAGAT | 51366 |
rs533495881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102405927 | CTTATAAGATCTACG[C/T]CCATGTAACTCAGTC | 51366 |
rs533548505 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102323225 | ACAACTTCACACCTC[A/T]AAGTCTTCCTTGATT | 51366 |
rs533572781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102326320 | TTTTAAAAGTAGCAA[A/G]TGATTCTTAAAGCCA | 51366 |
rs533610682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102322753 | CACCATGGAATCCTA[C/T]GCAGCCATAAAAAAT | 51366 |
rs533645185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102333955 | TTTGTGACACATCTA[A/G]TTAATCCTGGAAGTT | 51366 |
rs533663928 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102375083 | AAGTAATTTTTGGCC[A/G]GGCACGGTGGCTCAC | 51366 |
rs533725261 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102289668 | TTATTACATGTGAGA[C/T]ACTTGCTAGGATGTG | 51366 |
rs533744699 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102411228 | CGCCCATAGCAAACC[C/G]AACCCAGAAATTTAC | 51366 |
rs533755348 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102331907 | TCTGTGTTTCTCCCT[G/T]TATTCAAATTGTGCT | 51366 |
rs533756366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102368614 | TATTTTTTGTAGAGA[C/T]GAGTGGGGTGGGTGA | 51366 |
rs533771855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102354478 | ATCAACGAAAAGCAG[C/T]TTATACCTATCATCT | 51366 |
rs533828759 | in-del | -/AT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102355661 | CATCTGCAAACTCAA[-/AT]ATAAGTAAACAAATC | 51366 |
rs533829244 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102280228 | TGTGAAATGTATAAC[A/C/G]CAAGAATGTGTAAGC | 51366 |
rs533831404 | snp | A/G | 0 | 0 | intron-variant | UBR5 | GRCh38.p7 | 8:102273286 | AACTTAGAAAAATGG[A/G]CATATCAACTGAGTT | 51366 |
rs533842237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102361260 | ATGGTAAATACATCA[C/T]AGGGTTTACTCTTAA | 51366 |
rs533844760 | snp | A/C | 1.65734e-05 | 0.00287862 | intron-variant | UBR5 | GRCh38.p7 | 8:102360695 | AACAGAAAAAATTAT[A/C]CAAGTAAAAATGTGT | 51366 |
rs533865339 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102327971 | GGTAAAAACTAGGGC[A/G]AGGCATATATACTTT | 51366 |
rs533913855 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102383180 | GTCAATTTTTAGGAA[C/T]TGGAGGCATCACATT | 51366 |
rs533929134 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102395726 | AAAACATTCTATTCA[C/G]CAGTGTCAAGTCACA | 51366 |
rs533941282 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102401699 | TAATCTTCTATTGGC[A/G]ACTATAGGAGGCAAA | 51366 |
rs533981750 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102404608 | TGTCATACCGGAGGT[C/T]AAGAAGTTATAGCAC | 51366 |
rs533992075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102409088 | AACTCAAGAAATCCA[C/T]TGGAAAGGAGATCAA | 51366 |
rs534043936 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102411588 | CCTTCCCCCCACCCC[C/G]CGCCCGCTCCCAGCA | 51366 |
rs534047284 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102403728 | CTGTTGCCCAGGCTG[C/G]AATTCAATGACACAA | 51366 |
rs534059067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102272112 | GGTTGTAAAGTCCTT[A/G]TCTCACTGGGGACCA | 51366 |
rs534085528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102386449 | AGAAAAAAAGAAAAA[C/T]GAGCACGGAGACTGT | 51366 |
rs534087284 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102259445 | AATAGCTTCAATCTT[A/C/T]AAAAAGTGCTACCCT | 51366 |
rs534107519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102330823 | AGAGGGGAGTGCAGG[A/G]TAAAAACCAAACGGA | 51366 |
rs534126803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102266050 | CACCTTCATTCAGCT[A/G]TTGATGCATCCTGTG | 51366 |
rs534181492 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102336682 | AATTTACTTCTGGGC[G/T]CTCTACTCTGTTCCA | 51366 |
rs534195946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102285918 | CTAAACCACACTATT[C/T]TGGGGAGAGGAGTAT | 51366 |
rs534215207 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102320745 | AGCTTATCCACCATG[A/G]TCAAGTGGGCTTCAT | 51366 |
rs534230697 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102413986 | GGCATGGCTGTGCGC[A/G]CCTGTAAACCCCACT | 51366 |
rs534233021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102302853 | TTCATCTGTTCAACC[A/G]GCAGCCCTGAGTTTG | 51366 |
rs534293545 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102264409 | CAGTATGCTAGCGTT[A/T]GATTATTTTATAAAA | 51366 |
rs534298126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102358482 | ACAGTATAACCGGTA[A/G]TACTTATTCTTAAAT | 51366 |
rs534312177 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102365982 | ATATAACATATCTGC[A/G]TGTTCAAATACCCCT | 51366 |
rs534318946 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102348241 | CAAAAATAAATAAAT[A/T]AATTAATTAAATGAA | 51366 |
rs534355899 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102272981 | AAATTAAATCAGGAC[A/C]ACAGAATTTAATTCA | 51366 |
rs534375092 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102342949 | CTTTATTTTGAAGTA[C/T]ATTTGGTTCTTTTTT | 51366 |
rs534434233 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102350617 | CTCCTAGAAGGAAAC[A/C]TAAGGGAAAAGCTTC | 51366 |
rs534443241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102255494 | AGGTACTCTAGAGAT[A/G]AAGTTGATCTAAACC | 51366 |
rs534444728 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102394099 | AGACGGACTCTCGCC[C/G]TCGCCCAGGCTGGAG | 51366 |
rs534446009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102337223 | ATGTCATCTGCAAAT[A/G]CAGATAATTGTACTT | 51366 |
rs534458936 | snp | C/T | 1.70621e-05 | 0.00292074 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102345503 | ATAATGACACTTGGG[C/T]GGGCAGAATGAATGT | 51366 |
rs534480987 | snp | A/G | 0.000281973 | 0.0118704 | intron-variant | UBR5 | GRCh38.p7 | 8:102293944 | AACCAAAATCAAAAA[A/G]GATGCCTTACTTTTT | 51366 |
rs534528168 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102271372 | AGATTATCCTTCCCT[A/C]GCATCTGTGTTGTTA | 51366 |
rs534533266 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102396504 | TCTTTCGGATACACA[C/G]TATCACTCTTCAAAT | 51366 |
rs534568505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102284762 | AAGTTGGGGGTCGGG[C/T]GCTGTGGCTCACGCC | 51366 |
rs534579154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102328164 | TTGCTCTACCAATTT[C/T]TAAAAGAATTTAGTG | 51366 |
rs534581276 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102316034 | TAGTACAAAATCCAA[C/T]GTAATTAGAAAGTCT | 51366 |
rs534596808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102292262 | TTATGGGTAAGAATG[C/T]ACTGTACTATAATAA | 51366 |
rs534614857 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102337949 | CTAATTAAAAGATTA[C/T]CTCTTCTCACCAAAG | 51366 |
rs534638837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102380348 | GCAGGGAACCAAGAT[C/T]GTGCAACTCCAGCCT | 51366 |
rs534648563 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102335141 | AGGACATTATGCTAA[C/G]AGAAATAAGATAGAC | 51366 |
rs534656350 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102343797 | CAGAGATTGCAGTGA[C/G]CCAAGATCACACCAT | 51366 |
rs534672883 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102371495 | ATCTGACGCCCCATC[A/C]ATGAATTTTTCATAC | 51366 |
rs534698748 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102318841 | ATCCAGCCAAACTAA[C/G]CTTCATAAGTGAAGG | 51366 |
rs534699083 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102327226 | TCTTCCAAATAATTA[C/T]ACTTCATTAGGAAAC | 51366 |
rs534717650 | in-del | -/G | 0.485528 | 0.0838238 | intron-variant | UBR5 | GRCh38.p7 | 8:102343861 | GTCTCAAAAAAAAAA[-/G]GGGGGGGGTGGGCAG | 51366 |
rs534719181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102299075 | ATAAGCACATAGACA[A/G]TAGGGTACACTGCCT | 51366 |
rs534760398 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102305805 | TTCCAGGCTGTAGTG[C/T]GGTGATGTGAACACA | 51366 |
rs534843876 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102277691 | AGCCTTACCCACCCC[A/C/T]CTCCTTTAAATTCAC | 51366 |
rs534854425 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102413833 | TCAGAGTTTTGGCCA[C/T]GGCGCACAGTGGCTC | 51366 |
rs534870804 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102389568 | TTTCACCCATTAAGT[A/T]TGGGTTGGTTTACTG | 51366 |
rs534881549 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102328784 | AGTAGAGATGGGGTT[C/T]TGTATTTTTAGTAGA | 51366 |
rs534962445 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102284892 | AAACAAAAAATTAGC[C/T]GGGCGTGGGTGGCAA | 51366 |
rs534963571 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102410970 | CCTGTAAACATTTAG[A/C]CCATCATTAGATCTG | 51366 |
rs534986436 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102364139 | AGAACTCTTTTAGTC[A/G]TCTCCGGTTCTGAAA | 51366 |
rs534996092 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102414492 | TGAGGAAGGAAGGTA[A/G]ACCAGTAGACACTGC | 51366 |
rs534997753 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102268451 | TCAGGCAATCTGCCC[A/G]CCTCAGCCTCCCAAA | 51366 |
rs535050701 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102269348 | ATATTTGTATGACAA[A/C/G]TTTTCTTTTTAGGTT | 51366 |
rs535064542 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102318379 | TGAAGCGAGAAGAGA[A/C]GTTTAGAGAAAAAAG | 51366 |
rs535078890 | in-del | -/AAA | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102282665 | AGTGAAACTCTATTT[-/AAA]AAAAAAAAAAAAAAG | 51366 |
rs535079948 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102305670 | TACTTCATGTTATCT[A/C]TCTAATTAGAACCCT | 51366 |
rs535083195 | snp | C/T | 3.29804e-05 | 0.00406068 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102326567 | ACCAACAGTGATGTT[C/T]GGCATTGAAGAAATA | 51366 |
rs535088335 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102283334 | CAGTTGCTTAGGAAG[C/G]GGAAGGCGGGGGGGG | 51366 |
rs535094051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102370992 | CTGTATATATACACC[A/G]CATTTTTAACCAGTC | 51366 |
rs535118514 | snp | C/T | 1.73348e-05 | 0.00294399 | intron-variant | UBR5 | GRCh38.p7 | 8:102311919 | AAATGAGAAGAAAAA[C/T]TGTTATACATCTTAT | 51366 |
rs535144495 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102412480 | GCGGAGTGCGAGGCA[A/G]GCGGCCGGGACCAGG | 51366 |
rs535157764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102378219 | AATGATTCCTCTCTG[C/T]GTGGTATCACAACTA | 51366 |
rs535174614 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102386406 | GCACTCCAGCCAGGG[C/T]GACAGAGCAAGACTC | 51366 |
rs535201484 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102370213 | CCTCTGTGGCCCAAG[C/G]TGGAGTGCAATGGTG | 51366 |
rs535218524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102298243 | GGAATAATAAACACA[C/T]GAATTTCATACACAC | 51366 |
rs535221037 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102317599 | CAGTAGTTCTCCCAG[C/G]GTGCAGCTGGAGATC | 51366 |
rs535240258 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102297060 | TAATTATTTCTGGTA[C/T]TTTCTAGAACAATTC | 51366 |
rs535248481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102349938 | CAAAGGCGGGAGGAT[C/T]GCTGGAGGCCAAGGC | 51366 |
rs535251926 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102256015 | ACTCATGAGATTTAA[C/G]TTGGCTGACTGGACT | 51366 |
rs535277451 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102289848 | ATTCTACAGGAAGAT[G/T]TTTCCTCCTCCACCA | 51366 |
rs535298438 | in-del | -/A | | | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102253288 | CAGTGTATTGCCCTT[-/A]AGTTTAAAAATGTAC | 51366 |
rs535303263 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102407018 | CAATGTGGTAGTGAG[G/T]AGCTACGTGGCACTA | 51366 |
rs535320468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102339951 | CTGGTATGTCAAGAA[C/T]GTAGAAATAACACTT | 51366 |
rs535372548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102306222 | AGTTGTGGAATATTT[A/G]ATGAATCGAATATAA | 51366 |
rs535411887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102398863 | AAATGGGAGAAAATA[C/T]TTACAAACTATCCAC | 51366 |
rs535419311 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102398374 | TTTGAAATTTCCCCC[A/C/T]AAAAAACTGGGAAAA | 51366 |
rs535436455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102405586 | AACACTTTGGGAGGC[C/T]TAGGTGGGCAGATCA | 51366 |
rs535480168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102390693 | TAAATTTAACAAGTG[C/T]ACAAACTGGCCTATT | 51366 |
rs535501406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102260086 | ACATAGTAGGATTGA[C/T]GTTACTCTTTACAAG | 51366 |
rs535501732 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102264870 | TTGCAGCACAATGCC[C/T]GCTAGTATTTTTTTA | 51366 |
rs535503847 | in-del | -/GGACAAAAG | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102357635 | CCTGGACTGAATCCT[-/GGACAAAAG]GGTATTAGTGGACAA | 51366 |
rs535503916 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102397504 | CAGGAGTTCGAGACC[A/T]GCCTGGCCAATATGC | 51366 |
rs535512403 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102391777 | GCTGGTTAAAGTAAG[A/G]CTGAGACCTACTAGG | 51366 |
rs535519695 | snp | A/G | 0.000257129 | 0.0113357 | intron-variant | UBR5 | GRCh38.p7 | 8:102346893 | ATTAAGTGTTCTACG[A/G]GATCCATACCTGTGA | 51366 |
rs535532412 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102362342 | CTAGGTATTTTGTCA[A/T]CCTAAGAAAGTCATT | 51366 |
rs535543990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102361765 | AGAATGTTTTTCATA[C/T]TTTCATTTTTGTCCC | 51366 |
rs535552702 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102393399 | CCCAGCACTTTGGGA[C/G]GCCAAGATGGGCGGA | 51366 |
rs535571403 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102361965 | CCCAACCAAAGGCTC[A/G]ATTGTTTAAAAAAAC | 51366 |
rs535589205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102397056 | TTTGAAGAGGCCACA[C/T]AGTCAATCCCAGCCT | 51366 |
rs535600756 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102301522 | GTGGATGGGAGCATG[A/G]CACAGTGACTGTTTC | 51366 |
rs535649407 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102348790 | ATTTGATTTTCCAAA[C/T]CATTTCCCCCCTTAA | 51366 |
rs535663985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102298756 | TTTAAATTTACATAA[C/T]TATTGTCCATATAGT | 51366 |
rs535715712 | snp | A/G | 0.000247776 | 0.0111277 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102281302 | ACCTTTTGCGTTCTA[A/G]TTGAGGTGTATCCAA | 51366 |
rs535737528 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102342786 | TCTACTCATAAAAAT[C/T]TATGTAAATGTATAT | 51366 |
rs535759051 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102347975 | TCATGCCTTGTAATC[A/C]CAGCACTTTGAGAGG | 51366 |
rs535761669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102355855 | CTAAGGATTCTGTCT[A/G]CATTTTAAAGTCTTA | 51366 |
rs535764058 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102373107 | CTCTTGCCTCCCTGA[A/G]AGCTGGGATTACAGG | 51366 |
rs535775806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102391871 | CAGGTCATAAAGACC[C/T]TGCTGATAAAACAGG | 51366 |
rs535782067 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102252423 | TAAATATTTTCATTT[A/C]AGTAACTATTAAAAA | 51366 |
rs535825714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102338773 | GTGGTAGGATTAGGA[C/T]AGGAAATCCAGCAGT | 51366 |
rs535826074 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102331865 | CCTCCATCTCCCTGG[C/T]ACTACCATGCACTCC | 51366 |
rs535850340 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102272260 | ATTTTTATATCACTA[C/T]GTATTTTACAACCTC | 51366 |
rs535872223 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102321820 | CTTTGACAAACCTGA[C/G]AAAAACAAGCAGTGG | 51366 |
rs535921870 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102274405 | TGGGAAGTTGGCTAT[G/T]CAGTTTGAAAGAAAG | 51366 |
rs535943803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102374513 | TCCCTAACTAAATCA[C/T]ACTCACAAACTACTC | 51366 |
rs535963371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102353868 | GTCAAAACCCAGTCT[C/T]CACAAAAAAATAATT | 51366 |
rs536004936 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102317360 | CACTCTGAGATCAAA[C/G]CGCAAGGCGGCAGCC | 51366 |
rs536048809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102324771 | TAGTTCTTAAGATGA[C/T]CTATAAATACAGATG | 51366 |
rs536063043 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102307830 | GACACAACTCATTCT[A/G]GCTTTCCTCCAACCC | 51366 |
rs536083695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102353198 | AAAGACAGTACTGGA[A/G]TCAGTTGATTCCTTT | 51366 |
rs536121415 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102332647 | CACCTTAAAAATGCT[C/G]CTTAAATGCTATCTC | 51366 |
rs536122891 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102410065 | TGAAATTAAAAGTCA[C/T]TATGATCTAAATATT | 51366 |
rs536129982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102360017 | CTGAGAGCACTCACA[A/G]GAAGATGATACAGAC | 51366 |
rs536144080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102367392 | AGGCTATATAAACTT[C/T]GAGCCCTTTCTGATG | 51366 |
rs536155238 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102332137 | GACACGACAATCGAA[C/T]TGACTGATGAGAGAA | 51366 |
rs536164237 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102257104 | ACTTGATGGGTGGAC[-/G]TAAGTTCCACTAAGA | 51366 |
rs536174941 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102306089 | GGGATCATGACAGGT[A/G]TAATTTAATTAACAA | 51366 |
rs536175302 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102314597 | CAAAGAAGGTTATGC[-/A]AAAAAAAAAAAACCA | 51366 |
rs536195917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102308674 | TTTACTATACTTTCT[C/T]TGGTTACTTTAGAAT | 51366 |
rs536232473 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | UBR5 | GRCh38.p7 | 8:102322654 | ACGTATGTTTACTGC[A/G]GCACTATTGACAATA | 51366 |
rs536245010 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102330636 | TTCTACTTCATATTC[G/T]CTTCTCAATCCTACG | 51366 |
rs536249423 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102401096 | GGGAAAAGCCACCAC[A/G]ATCCATGATTTTACT | 51366 |
rs536259575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102408415 | CACCTGAAAGGGAAA[C/T]TCTAAGCTTAGAGAA | 51366 |
rs536285288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102315049 | ATGCATGCTTTCAAA[C/T]AGTGGTTTAATATGG | 51366 |
rs536321614 | snp | C/G/T | 4.94347e-05 | 0.00497145 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102286528 | TCTCCTGTTCTATGT[C/G/T]GTCACTCTGACTACT | 51366 |
rs536322076 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102314455 | GAGTCTCAACAAAAG[G/T]GAGTAGATAGACTAG | 51366 |
rs536330733 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102381969 | TAACTTTTTTGATCT[C/G]AGGAAAAAGAAACAT | 51366 |
rs536358189 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102285854 | TGGGATTATATATAC[G/T]TACGTAAATCTAAAT | 51366 |
rs536387253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102270411 | ACCTTAACATACCAG[A/G]TATCAAGAGTCCACA | 51366 |
rs536455558 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102410952 | AATGCTCCACTTTGT[G/T]ATCCTGTAAACATTT | 51366 |
rs536472736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102292499 | AGTGTTTAGAGATGA[A/G]ACGATCCCAAAATCT | 51366 |
rs536488793 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102317023 | AAGACAGGTGATTTC[C/T]GCATTTCCATTTGAG | 51366 |
rs536500007 | snp | A/G | 1.65597e-05 | 0.00287743 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102265120 | AATGTTTCTGAAACA[A/G]TTCAACCTTGCTTCT | 51366 |
rs536506441 | in-del | -/G | 0.0170251 | 0.090679 | intron-variant | UBR5 | GRCh38.p7 | 8:102287189 | AAAAAAAAAAAAAAA[-/G]GGCAAGAAAATAAAA | 51366 |
rs536544975 | snp | A/G | 3.2962e-05 | 0.00405954 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102360170 | GTCCTCCCTGCCCCC[A/G]AGTTGCTGTTCAACT | 51366 |
rs536558382 | snp | A/G | 0.000199554 | 0.00998686 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102300015 | CAGGATCCATCGCAG[A/G]AGGGTCAGGAACCCA | 51366 |
rs536562075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102351580 | ACTTCACAAGATGAA[A/G]AAGTTCTAGAAAGCT | 51366 |
rs536590338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102272909 | AAAGTAATTGGAGTT[C/T]TCAGAAGCTTATCCA | 51366 |
rs536668922 | snp | A/T | | | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295062 | TTTGCTGATTGAGGT[A/T]TACTTGCTCTTCTGG | 51366 |
rs536671182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102393343 | AAAGTTAATTCTGAA[C/T]GTAAAAACGGAAACA | 51366 |
rs536704747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102263218 | ACTGGTTTCATTTCA[A/G]TTAGAGTTGCAGTTT | 51366 |
rs536725001 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | UBR5 | GRCh38.p7 | 8:102320619 | TCCTGATACCAAAGC[C/T]GGGCAGAGACACTAC | 51366 |
rs536743491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102357625 | CAACTGGGATCCTGG[A/G]CTGAATCCTGGACAA | 51366 |
rs536749050 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102364883 | GAATCACTGCAGGCC[A/T]GTGATAACATTCGTT | 51366 |
rs536749125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102373240 | CAAACAAGAAGAAAT[C/T]TGGTAAGAAAAGATT | 51366 |
rs536760551 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102306811 | CTCTCACACTGAGAG[A/T]ATCAATACTACTTAG | 51366 |
rs536771382 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102325068 | CTAGTACATGAGTGC[A/G]ATTGAAAAATAATGT | 51366 |
rs536789040 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102348047 | CTGGCCAACATAGAG[A/G]AACCCTGTCTCTATT | 51366 |
rs536791491 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102277671 | AGGCATAAGCCAGCA[A/C]AACCAGCCTTACCCA | 51366 |
rs536841274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102293013 | GATCCTAAAGGTCCT[C/T]ATTAAAACATCATCA | 51366 |
rs536862258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102395516 | TGTTCACATTAATAT[A/G]TAATTACATACACAC | 51366 |
rs536876237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102300954 | AACTAACAATGATTT[A/G]AGAGAGCACAAAAGG | 51366 |
rs536895671 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102406703 | CTAATGTCTGGGGGG[-/T]TTTTTTTATTGATTT | 51366 |
rs536901825 | snp | A/T | | | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303539 | AAAACTATATCCTGA[A/T]TTCTTCATATTCATT | 51366 |
rs536904616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102270809 | CAGGCGTGAGCCACC[A/G]CATGTGGCCTGAAAA | 51366 |
rs536905221 | in-del | -/TCACCTGAGG | 0.00716266 | 0.059414 | intron-variant | UBR5 | GRCh38.p7 | 8:102339307 | GCCGAGGAGGGTGGA[-/TCACCTGAGG]TCAGGAGTTCAAGAC | 51366 |
rs536981019 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102395010 | TAGTTCCTCAAATAC[A/C]CAGCAGTCTCTCACG | 51366 |
rs537021420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102378141 | AAATTAAAAAAAACT[A/G]CCATAGCCAAATTTA | 51366 |
rs537036004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102326478 | CATCTGTAAAACTGC[C/T]TACAAGGGAAGAAAG | 51366 |
rs537067477 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102315054 | TGCTTTCAAATAGTG[C/G]TTTAATATGGGAAGG | 51366 |
rs537084328 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102350546 | AAGTTGAACCCTTAT[C/G]TTACATTATATACAA | 51366 |
rs537127016 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102377438 | ACTGGCCAGGCGTGG[A/T]GGCTCACGCCTGTAA | 51366 |
rs537164551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102297685 | TTCAACTGGAAAGCC[C/T]TAGCATACACACAAT | 51366 |
rs537187134 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102253525 | CCAGGCTGAGTTTAC[A/G]TAACTGAAATACCTT | 51366 |
rs537221088 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102393095 | CTCCACAGGGGCAGA[C/T]ATTTTTGCCTGTTTT | 51366 |
rs537231451 | in-del | -/ATATAC | 0.0433465 | 0.140692 | intron-variant | UBR5 | GRCh38.p7 | 8:102396676 | CACACATATATATAT[-/ATATAC]ACACACACACACACA | 51366 |
rs537242012 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102406864 | GAAGATATGCCTGAG[C/T]CTTTAAAACCTCAAA | 51366 |
rs537278049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102364027 | TGGAAACAATGCCAC[C/T]GAATAGCAAGAAATC | 51366 |
rs537303074 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102334980 | TGGTAGTATTTATAA[C/T]AGGTAATATATGGAA | 51366 |
rs537303872 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102351163 | TTAAAAGAACTACCA[C/T]ATGATCCAGCAATTG | 51366 |
rs537341963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102363055 | GGGGTTTCGCCATTT[A/G]GGCCAGGCTGGTCTC | 51366 |
rs537354092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102370920 | TGTCCTCCTGGCTCA[C/T]CCATGTTGTTGCAAA | 51366 |
rs537382192 | snp | C/T | 0.000330115 | 0.0128432 | intron-variant | UBR5 | GRCh38.p7 | 8:102275666 | TCCCTGAAATACATG[C/T]TTATCAGGCAGAATG | 51366 |
rs537388764 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102267843 | TCAAACTGGGTATCA[C/G]ATTAGCCCCAGGATA | 51366 |
rs537405804 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102400776 | TCCAATTTCGTGGTT[-/A]AAAAAAAAAGAAGCG | 51366 |
rs537419354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102282530 | AAAAAATTAGCATTG[C/T]GGCGGGTGCCTCTAA | 51366 |
rs537487826 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102403304 | TAATCCCAGCACCTT[C/G]GAGAGGCTGAGACGG | 51366 |
rs537507473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102289736 | ATACTTAATCTATAT[A/G]TCAGAAAATATAAAT | 51366 |
rs537514026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102411354 | AAAACACTATCATTA[A/G]AATAGAAAAGGAAAC | 51366 |
rs537519222 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102324421 | AAAAAAAAAAAAAAA[A/C]CTCTGTCAGGGGACT | 51366 |
rs537525521 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102317082 | CAGACAGTAGGCGCA[C/G]GACAGTGGGTGCAAC | 51366 |
rs537527869 | snp | A/G | | | intron-variant, utr-variant-5-prime | UBR5 | GRCh38.p7 | 8:102302349 | TTTTGACATTTCTTC[A/G]TAAAGGCTTGCCTGG | 51366 |
rs537536634 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102360786 | CGATAAATAAACTTC[C/T]TTCCAAAAGGTGCTT | 51366 |
rs537594798 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102313109 | TTAAGCCCGTATCTA[A/C]TTCTCAGAAGAAAAC | 51366 |
rs537602188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102306324 | GTGGGAGTATAAAGG[A/G]AAAAAAAAAACTGCA | 51366 |
rs537659294 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102406436 | GTAGCTGCAACTACA[G/T]GCATGCACCACCATG | 51366 |
rs537665220 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102269178 | TACATCTACAATCTT[A/T]TATTTAAAAAAAAAA | 51366 |
rs537682305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102312652 | GACTCTGAGCTTTGC[C/T]ACTGACATCTATATT | 51366 |
rs537684984 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102347897 | GCGAAAATAATTTTT[G/T]AAAGCCACCTATGTA | 51366 |
rs537717550 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | UBR5 | GRCh38.p7 | 8:102318257 | AAAGGAGCTGATGGA[C/G]CTGAAAGCCAAGGCT | 51366 |
rs537719070 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102413834 | CAGAGTTTTGGCCAC[A/G]GCGCACAGTGGCTCA | 51366 |
rs537744843 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102355210 | AAATGTGGCTCTCAA[A/T]GAGACTATTCACTTC | 51366 |
rs537745420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102347414 | TGGGGATTATAGGCA[C/T]GCACTACCATACCTG | 51366 |
rs537787572 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102405540 | AATATGTATAATATG[C/G]GCGAGCGCAGTGGCT | 51366 |
rs537802863 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102311029 | GATCTGTCCGGGTAT[C/T]GCTTCTTAAAGAAGT | 51366 |
rs537808062 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102389961 | AGACAGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 51366 |
rs537819197 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102361513 | TCATATCAGGCTGCC[A/G]CCTAAATGAGTTTTT | 51366 |
rs537821865 | in-del | -/AAGA | 0.00755907 | 0.0610114 | intron-variant | UBR5 | GRCh38.p7 | 8:102313712 | AATAAAACAGCCCTG[-/AAGA]AAGGACTCAGATATC | 51366 |
rs537826467 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102392557 | CAGGAAAAAAAAAAA[A/G]GTAAAGTTATAATGT | 51366 |
rs537834995 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102404700 | AACACCTGAGGTCGG[C/G]AGTTCGAGACCAGCC | 51366 |
rs537859522 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102325312 | ATGAGGAAGACCAAG[-/A]AAAAAGGTATCATGA | 51366 |
rs537860083 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102411761 | CTCTCTTTTTACCTC[C/T]ACCATCCCCCATCCG | 51366 |
rs537865575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102266834 | TCTACTGTAAACATT[C/T]ATTTTATTTATAAAG | 51366 |
rs537870747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102396637 | ATATATATATATACA[C/T]ACATATATATATACA | 51366 |
rs537890447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102266133 | CTCTTTTGAAGTTCC[C/T]GTGTGTGTCTGCTGA | 51366 |
rs537922852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102369203 | TATATGAAGAAAAGC[C/T]GGCCCTAGATAGAAA | 51366 |
rs537923240 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102330087 | TTGGAATGCAATTAA[A/T]TTATAAAAAGCTTGG | 51366 |
rs537981340 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102402626 | ACAAGGAGGCTGTCA[C/T]GGAAAACACCCAAAT | 51366 |
rs537984169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102376197 | AGTTGTTTTAAGAAA[C/T]AGGTAACATCACATG | 51366 |
rs537986145 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102324565 | CCAATATCCCAATCT[C/T]ACTATGTGGTAGATG | 51366 |
rs538030906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102296757 | TATTATACATAAACT[A/G]ACTTAAACAAGGGAA | 51366 |
rs538059201 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102398273 | ATCGGATGTCCATAT[C/G]CAGAAGAATAAAACT | 51366 |
rs538121277 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102279795 | TGGGTTCTCAAAAAA[C/T]AGCAATTAGGCCAAC | 51366 |
rs538152602 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102294848 | GCCACCCCATCCCTA[A/C/T]CTGAGTGTGTTATTA | 51366 |
rs538160946 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBR5 | GRCh38.p7 | 8:102304789 | CCTCAATGTAACTTG[A/G]CTTAACCTGCTAAAT | 51366 |
rs538202051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102381167 | GGCCAGGAGTTCAAG[A/G]CCAGCCTGGTCAACA | 51366 |
rs538245954 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102345575 | AAACATCACTGCAGC[A/G]TACACACAAAGAGCA | 51366 |
rs538254452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102375874 | TTAACATGAAAATTA[C/T]AGGAAGTCCGATCAC | 51366 |
rs538261481 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102382083 | AAGTGATTTACTTGT[A/T]GTTACTCAGTTAAGA | 51366 |
rs538265505 | snp | A/C | 0.0279526 | 0.114869 | intron-variant | UBR5 | GRCh38.p7 | 8:102380393 | GACTCAAAAAAAAAA[A/C]AAAAACAAAAACAAA | 51366 |
rs538266545 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102302960 | CAACACATCACCCAC[G/T]CTTGAAGCTCCTTTT | 51366 |
rs538279019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102345626 | CTCTAAAAATTCACA[C/T]ACATTTAAAAACTAG | 51366 |
rs538311612 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102383135 | TTCAACCTAAACCCT[A/G]CGTGGTAGGAGGAAG | 51366 |
rs538312999 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102335784 | GAACTCCTGACCTCA[G/T]GTGATCCACCCGCCT | 51366 |
rs538326153 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102370991 | ACTGTATATATACAC[A/C]ACATTTTTAACCAGT | 51366 |
rs538326294 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102397177 | GAAAACTGAAGAGGA[C/T]AAACCAGTCCCCACA | 51366 |
rs538327360 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102284968 | CATGAACCCAGGAGG[A/C]GGAGCTTGCAGTGAG | 51366 |
rs538336573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102353080 | CACCTACCAGTCCCC[A/G]TACGTCAATCGCCAT | 51366 |
rs538350221 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102411461 | GCACTTCCCCACCCC[C/T]GCTTGAATCCATCCC | 51366 |
rs538350629 | snp | A/G | 0 | 0 | intron-variant | UBR5 | GRCh38.p7 | 8:102352285 | CTGCACTCCAGCCTG[A/G]GTGACAGAGTGAGAC | 51366 |
rs538356117 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102309837 | GTAACTAGAATCTAG[A/T]CACATTTCACTCCTA | 51366 |
rs538378483 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102291969 | CTGTCTACAATACTT[A/G]GGAAAGTTCCTAGTA | 51366 |
rs538409312 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102309346 | AGGTACAATCCACCA[C/T]GCCCGACTGTGTACA | 51366 |
rs538411255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102280296 | AAGAAAAGAGAAATT[C/T]CCACCCAGACAGAAA | 51366 |
rs538466784 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102409241 | TTCTTTCCACCCCAG[C/G]CATCCCCACCTGTAT | 51366 |
rs538508057 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102272239 | ATGCTGCAATTTGAT[C/T]GGTGAATTTTTATAT | 51366 |
rs538525365 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102317685 | CCTAACTGGGAGGCA[C/T]CCCCCAGTAGGGGCA | 51366 |
rs538538264 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102366222 | TGGCAAAAGTGGCAT[A/C]ATCTGCCACCAGTGC | 51366 |
rs538593224 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102374419 | AGTTTTTATTTCAGC[G/T]TTTTTTTTTCTTCTG | 51366 |
rs538597332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102271557 | TGTCACTATAAATAA[C/T]GCTGAAATTTCTTAC | 51366 |
rs538612911 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102329876 | AACTTAAGAACTTAG[C/T]GTACAAGTAGGTGCT | 51366 |
rs538613059 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102277703 | CCCCCTCCTTTAAAT[A/T]CACTTCTTGGCCTGA | 51366 |
rs538622497 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102320922 | TCAATAAATTAGGTA[C/T]TGATGGGACGTATCT | 51366 |
rs538647384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102388771 | TATTTCACATTTCCT[A/G]AACAATGCACCTAAT | 51366 |
rs538648435 | in-del | -/TCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGTGGA | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102274466 | GCCAGGTGTGGTGGC[lengthTooLong]TTACTTGAGGTCAGG | 51366 |
rs538672227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102336447 | AAAATCACTGCCATG[A/G]GCAATGTCAAGGAGC | 51366 |
rs538792867 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303917 | TTTCCCAGGGTGTTA[C/T]TGGGAGGAACAAAAA | 51366 |
rs538803104 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102276367 | TTCCTTCAAAGTGAT[A/C]AAGTCCATCTTAAGT | 51366 |
rs538824863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102409950 | CTAGATACAACCATA[C/T]AGCTCTTTATAATTT | 51366 |
rs538878252 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102315865 | GCTAATATTTGAAAT[C/G]GCTGATTTCAAGGAA | 51366 |
rs538884006 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102351541 | AAAAAAGAGCTCTTG[C/T]TATTTAACGGGTATA | 51366 |
rs538905914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102321586 | AGAATTGGAAAAAAC[C/T]ACTTTAAAGTTCATA | 51366 |
rs538919963 | in-del | -/TG | | | intron-variant | UBR5 | GRCh38.p7 | 8:102336336 | TTTTATTTTGTTGAC[-/TG]TTTTCTTTACTATAC | 51366 |
rs539006397 | in-del | -/A | 0.00953873 | 0.0683987 | intron-variant | UBR5 | GRCh38.p7 | 8:102407848 | CATTGAAGATCATCT[-/A]AGGATGGGCTTCCTT | 51366 |
rs539042185 | snp | A/T | 0.000165393 | 0.00909226 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102297587 | TACATCTTCCTCTTT[A/T]TCACTTGAGGATATT | 51366 |
rs539077394 | in-del | -/CTG | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102262546 | GCTGTTTCCTAAACC[-/CTG]CTGAAGACTCAATAT | 51366 |
rs539083455 | snp | A/G | 1.65778e-05 | 0.002879 | intron-variant, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102276947 | GCTGTACTGAACAAT[A/G]AAAACAAAGGGTCTT | 51366 |
rs539095661 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102414558 | TTTTTTTTGAGACGG[A/C]GTCTTTGCTCTGTCG | 51366 |
rs539096087 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102306280 | TCATTTTAACTATAA[A/C]TAGAAAAAAGCAGGT | 51366 |
rs539111135 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102406218 | CTTAAGCAAATTCAT[G/T]TAAACATTTTAGTTA | 51366 |
rs539119179 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102372131 | TTTGGTGAAAAGCAA[A/T]CTGATCACAGTCTTA | 51366 |
rs539122754 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102288524 | GGCCAACATGGTGAG[-/A]CCCCGACTCTACTAA | 51366 |
rs539151133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102261502 | GGTCAGGAGATCGAG[A/G]CCATCCTGGCCAACA | 51366 |
rs539166944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102305738 | TTTATTCCAGGCTTA[C/T]TCCCACCTTCTTAGG | 51366 |
rs539174474 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102389123 | TGGTTTAAAAGAAAT[C/T]TATAAATTATTTTAT | 51366 |
rs539176599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102379447 | TATCAATAAATAATA[C/T]TGCCATAATATTGTC | 51366 |
rs539177680 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102312587 | TTAAAGGAATCCAAT[A/T]CTTTGTATGTTTCTT | 51366 |
rs539180828 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102371620 | GAGTCACGGAGTCTC[A/G]CTCTGTCGCCCAGGC | 51366 |
rs539193180 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102317330 | CGCTCAGAGTCTCGC[G/T]GATTGCTAGCACAGC | 51366 |
rs539225798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102291504 | TGTCCCCCTCACATA[C/T]ATAAAGCTAAACATA | 51366 |
rs539230753 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102327293 | TTAACTCCTTAAAAC[A/G]CAACAAAGAAAAAAT | 51366 |
rs539234504 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102354764 | TTAGCAAAATCTTCT[A/G]AGGAAAAAACATTAA | 51366 |
rs539239688 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102401032 | TGCTGCTCCTGATGA[C/T]GGTCCATCCCATGAG | 51366 |
rs539243531 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102283446 | TGATGAAGGGCTGAA[A/T]AACTATGGAATTGGA | 51366 |
rs539265057 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102299138 | GTTACAATTTTTTTT[A/T]AAAAGAATATTCTGG | 51366 |
rs539294911 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102328477 | TTTAAAGCCAAATCG[A/G]TAATTTGAGACATAA | 51366 |
rs539301686 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102334569 | AGTGCTGGGATTGCA[A/G]GCATGAGCCACCAAG | 51366 |
rs539312158 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102341674 | GAAAATTTCCTACCC[A/G]AATGGTTCTGGAAAT | 51366 |
rs539321754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102290515 | ACTAAAGAGATTTCA[A/G]TATTAAAACATAAAA | 51366 |
rs539356152 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102298012 | TCCTTAATGCTTTCT[A/G]TTTAGCAGGAATTCT | 51366 |
rs539368961 | snp | A/T | 0.00080064 | 0.019992 | intron-variant | UBR5 | GRCh38.p7 | 8:102263098 | TCTCAAAAAAAAAAA[A/T]AATTAATTAATTAAA | 51366 |
rs539407836 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102376560 | CCCAGGCTGGAGTGC[A/C]GTGGTGCAATCTCAG | 51366 |
rs539463229 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102262996 | GAGGCTGACACAGGA[C/G]AATCACTTGAACCTG | 51366 |
rs539464508 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102384311 | TAGAATATTAAAGGT[A/T]TTATTTGTGTTTAAA | 51366 |
rs539465447 | in-del | -/TGATCTAAAACGCTTTCAGA | 0.00725212 | 0.0597785 | intron-variant | UBR5 | GRCh38.p7 | 8:102258093 | TAAAACGCTTTCAGA[-/TGATCTAAAACGCTTTCAGA]TGATGCCAATGCTAC | 51366 |
rs539472109 | in-del | -/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102315318 | AAGAAACTCTACTCA[-/C]AATGGTTTATAAAAA | 51366 |
rs539477232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102348886 | TCCTCTCACTTGACT[A/G]GAAAGCCCAATCTCT | 51366 |
rs539494924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102339699 | CTTAATATTTAAGAG[C/T]ATTGTATTAGGTCAT | 51366 |
rs539509722 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102286709 | AAACATACATATTAA[A/G]CAGAATGCCAGATTG | 51366 |
rs539509788 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102256191 | ACCTGTAGTCCCAGC[C/T]ACTCGGGAGGCTGAG | 51366 |
rs539550192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102355517 | CTATAAAGGAAAATA[C/T]GTGTGACTGTAAAAA | 51366 |
rs539554370 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102290298 | GGTTCTTTCCTATCT[C/G]AGTTGCTATGAGAAA | 51366 |
rs539577426 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102408905 | TAGTTGTATCCCTGC[A/G]TAAACACTGTAAATC | 51366 |
rs539586418 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | UBR5 | GRCh38.p7 | 8:102397643 | GAGGTGGAGGTTGCA[G/T]TGAGCCGAGATTGCC | 51366 |
rs539591652 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102259739 | CAGGGATCAGAAACA[C/G]TCAACACCATCAGTC | 51366 |
rs539596096 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102378866 | CCCACTCTCATCTTC[A/T]CCCAGTAGATACAGG | 51366 |
rs539604010 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102263923 | GTAGAGTCAGAGTCT[C/T]GTACGTTGTCCAGGC | 51366 |
rs539617964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102370731 | CATCCTACCTTCCCC[A/G]CTACCTTTCCCAGCC | 51366 |
rs539624050 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102413539 | TGCAATGGCGCGGTC[C/T]CGGCTCACCTCAACC | 51366 |
rs539647788 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102373545 | CAGATAATGTATTCA[A/G]ATTACTACAAATCCA | 51366 |
rs539661070 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102342352 | AAAAATATTGTTTTA[C/T]ATATTTGTGTTTTTC | 51366 |
rs539705231 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102264875 | CACAATGCCCGCTAG[-/T]TATTTTTTTATTTTT | 51366 |
rs539730846 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102289936 | AATAGAAGTGATCTA[A/G]CTTTTAAGAGATCTG | 51366 |
rs539736734 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102367505 | TTCAATGCAAAGGGT[A/G]TCCCAACCCCAAATC | 51366 |
rs539739226 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102340917 | TGCACTAAAAGTCTA[C/T]ACAGTGCCAAGATTT | 51366 |
rs539751512 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102385889 | TACAAAGTAGGTACT[C/G]TGTGGATTGACTAAA | 51366 |
rs539791025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102377406 | GCCTAAAATCATATC[A/G]TTAAAAAATGTACAA | 51366 |
rs539803800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102310024 | GAAATTGCTCCAATA[A/G]CTTCTAATGCACTGT | 51366 |
rs539805119 | in-del | -/A | 0.184521 | 0.241273 | intron-variant | UBR5 | GRCh38.p7 | 8:102349656 | CTTAACAGTAGCGTC[-/A]AAAAAAAAACAAACT | 51366 |
rs539824419 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102324863 | GCAGCTGTAACTGCC[A/C]TCAGCCTCCAGTATT | 51366 |
rs539825003 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102393178 | TTTGTTGACTAACAA[G/T]GAATGAATGAAACTT | 51366 |
rs539825776 | in-del | -/A | 0.28052 | 0.24813 | intron-variant | UBR5 | GRCh38.p7 | 8:102289166 | CGAGACTCTGTCTCC[-/A]AAAAAAAAAAAAAAA | 51366 |
rs539826142 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102396161 | CTCCTAAATACCTAT[C/T]AGAGTAAGTACAAAA | 51366 |
rs539896120 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102288490 | GCGGATCACAAGGTC[A/C]AGAGATCAAGACCAT | 51366 |
rs539926737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102359616 | ACGCCAGTATATAAA[C/T]TGACAAGCAAAACCT | 51366 |
rs539946892 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UBR5 | GRCh38.p7 | 8:102296007 | AGGTACTCTAAGGTA[C/T]AATCACTTTTGGAAT | 51366 |
rs539995776 | snp | C/T | 0.0648419 | 0.167978 | intron-variant | UBR5 | GRCh38.p7 | 8:102318063 | GAACGCAGTTCCTCA[C/T]CAGCAACGGAACAAA | 51366 |
rs540000329 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102264151 | GTTGTGTTTCTTACC[A/C]ATTTATAAATGGGGA | 51366 |
rs540034177 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102368002 | TTCAGACACATTTTT[A/T]AAAATCCATTTTTTA | 51366 |
rs540044388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102390746 | AGCCACTGCTAGTCA[C/T]AGGATGTTAATCTGA | 51366 |
rs540068352 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | UBR5 | GRCh38.p7 | 8:102317621 | CTGGAGATCTGAGAA[C/T]GGGCAGACTGCCTCC | 51366 |
rs540110774 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102370252 | ACTCACTGCAGCCTC[C/T]GCCTCCCGGGTTCTA | 51366 |
rs540147871 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102353267 | AAACTAACAAGTACT[A/G]GGAAAACCTGTTTCT | 51366 |
rs540163516 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102345050 | GATTTAAAATAAACA[C/G]ATCACTTATTTTAAC | 51366 |
rs540188378 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102301309 | TATGTTCAAGAGCAT[A/T]TCTATTTTATAAGAT | 51366 |
rs540191232 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102381657 | GTGAGGAGTCACAGA[-/T]TTTTTTTTTAAGGTA | 51366 |
rs540202189 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102381992 | AGAAACATACAGATA[-/T]TTCCATTTAATAGTG | 51366 |
rs540204017 | in-del | -/T | 0.00874735 | 0.0655527 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102414539 | CAGATCTAAAAAAAA[-/T]TTTTTTTTTTTGAGA | 51366 |
rs540263785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102300275 | CTCCAGGCAAGGGAA[A/G]TGAAGTACAAATGCC | 51366 |
rs540267114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102309570 | CCCTATCAGGTGCAC[C/T]TTTTTTTTATCCTTT | 51366 |
rs540270553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102410243 | GTGCCCAACACAACC[A/G]CAAAATAGGTTTTGG | 51366 |
rs540281477 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102264651 | ATTTTGAGAAATTCT[C/G]TACAGCCTCCTTTCT | 51366 |
rs540284612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102409595 | CATTTTATTTGTGAC[C/T]CTCATACATTTCTCA | 51366 |
rs540300298 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102373340 | TTTGTTTAACAGTAA[A/G]ACTATATATACATTC | 51366 |
rs540347996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102299314 | CACTGACAGATGGAA[C/T]GTAATTCAGAGAATT | 51366 |
rs540360138 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102370698 | CTGTATTTTTGTACC[C/T]GTTAACCAACCTGTC | 51366 |
rs540366933 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102308497 | GCTGAAAAGTTCCTA[C/T]TGCCTAGTGACATCG | 51366 |
rs540392371 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102399878 | TTGAACCCAGGAGGT[-/G]GGGGTTGCAGTGAGC | 51366 |
rs540408895 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102322139 | AAAGAAACTACCATC[A/G]GAGTGAACAGGCAAC | 51366 |
rs540428074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102390062 | CCACGCCCAGCCAAG[A/G]AGGATTATTTTTTAA | 51366 |
rs540430800 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102365647 | ACATTTATTCTATAT[A/T]CTGATTAAATAAACT | 51366 |
rs540466173 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102294579 | CCAATTTTCACAGTT[G/T]GGTTGTTTGGTTTTT | 51366 |
rs540468693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102330039 | TTTAAGGTAATCATT[C/T]GTTCACTTTTATGTT | 51366 |
rs540482952 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102329528 | ACAACTATACGAAGT[A/C]TTTAGCACAGCCTAC | 51366 |
rs540500922 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102410013 | TGCCACCTTGATGCA[C/T]ATGTTATGACTCAAG | 51366 |
rs540514670 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102321174 | CAGATGACATGATTG[G/T]ATATCTAGAAAACCC | 51366 |
rs540607965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102276511 | CCTCTAATTCTCTCC[A/G]GTCTGTTTCTGCACA | 51366 |
rs540615599 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102292698 | GGGATAGATTTGACA[A/T]GTCTGAAGATACACA | 51366 |
rs540625931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102395085 | TCTTAACACCTTGTC[C/T]TACGTCCTACATCCT | 51366 |
rs540650488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102319078 | CAGGATCAAATTCAC[A/G]CATAACAATATTAAC | 51366 |
rs540673246 | in-del | -/AA | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102362013 | TGTGTTATCCATGTC[-/AA]GAGATTCTTGAGTGC | 51366 |
rs540690919 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102401115 | CATGATTTTACTACA[A/C]TTTGACTAGGTTATG | 51366 |
rs540696513 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102276147 | CTCCCAGATCCACCT[C/G]TAGTTCAAACTTTCA | 51366 |
rs540715557 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102316678 | AAAAAACGTTTACCA[A/G]TTCTTTACAGATATT | 51366 |
rs540724267 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102345722 | AAATGCATAAATGTC[A/G]CCTGAGCTACTTACT | 51366 |
rs540728349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102351655 | ATATACTTAAAAATG[C/T]TTATAATGGTAAATT | 51366 |
rs540734245 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102283050 | ACAAAAATCTATACA[A/C]AAAAGTTCATATGAG | 51366 |
rs540747078 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102291879 | CCTAACTTTTCTGAG[A/C]CGTAGTTTCCCCATT | 51366 |
rs540756385 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102390994 | TTGGGAGGCCGAGGC[A/G]GGAGAATCCCTAGAG | 51366 |
rs540780250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102374545 | TTTATTTTTGTTTAC[A/G]TAACTATTCCCTCAG | 51366 |
rs540796963 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102279615 | ACTGACAAATCCAAA[C/G]AGAGGAGATGATCAG | 51366 |
rs540800002 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102368066 | TACTCCAACTTTGGG[A/G]TTTCATGGTGAAGGT | 51366 |
rs540844846 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102381413 | GAGAACTCACTATCA[C/G]AAGAACAGCAGCATG | 51366 |
rs540848024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102400724 | TATCTCACAGTTGTG[C/T]AGAGGACCTAGAATT | 51366 |
rs540866752 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102407929 | CTATCCTATGCATTA[C/T]AGGATGTTTAGCAGC | 51366 |
rs540879095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102407240 | GCACAAGCAATTCTC[C/T]TGCCTCAACCTCTTG | 51366 |
rs540902213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102277865 | ACCCATGCGTGGTGG[C/T]GGGCACTTGTAATCC | 51366 |
rs540936792 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102394217 | ATTCGCACACCACCA[C/T]GCCCAGCTAATTTTT | 51366 |
rs540942420 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102414683 | GGATTACAGGCGCTG[C/T]CACCATGCCTGGGTA | 51366 |
rs540991460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102363356 | AAGAAAGTTAAGCTT[C/T]TTCAAAGAATTCCAG | 51366 |
rs541038924 | in-del | -/A | 0.00517822 | 0.0506191 | intron-variant | UBR5 | GRCh38.p7 | 8:102381498 | GTGGGGATTATGGGG[-/A]TCACAATTCAAGATG | 51366 |
rs541065151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102409072 | GCAGGAACGTAGTAC[C/T]AACTCAAGAAATCCA | 51366 |
rs541085041 | snp | C/T | 0.000155053 | 0.00880356 | intron-variant | UBR5 | GRCh38.p7 | 8:102261108 | TTAAGACACAAATAG[C/T]CTCATTGGATCACAC | 51366 |
rs541127697 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102290757 | CAGGAATTTAAGACC[A/C/G]ACCTGGGCAACACAG | 51366 |
rs541137762 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102342021 | AATCAAAGAACACAG[A/T]TCCCTAATCTTGTCA | 51366 |
rs541148096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102378472 | AACATGGTGAAATCC[C/T]GTCTCTACTAAAAAT | 51366 |
rs541150447 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102317709 | AGGGGCAGACTGACA[A/C]CTCACACGGCCGGGT | 51366 |
rs541157687 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102308466 | TATGACTGTGGTACT[A/G]TAAGATTATAATGGA | 51366 |
rs541200450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102357684 | TTAAATAAACTCTGT[A/G]TATTAATCAGTGATC | 51366 |
rs541214612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102370363 | GTAGAGACGGGCTTT[C/T]GCCATGTTGGCCAGG | 51366 |
rs541238832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102263430 | CTTAGTCTATTCCAT[C/T]TGTTTTGTGTCAAGT | 51366 |
rs541243626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102255016 | AATCATTTTATAATA[A/G]TAATTATTGGGGAAC | 51366 |
rs541260155 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102290093 | CCCTAAACACCTGAT[G/T]TGGAGACAACCAAGA | 51366 |
rs541266764 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102314516 | CATGAATTTCACATA[A/T]CTTTTTAAAACTCTA | 51366 |
rs541269123 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102392141 | TTCTATCAGTATATG[C/T]TACCAGTGTGATTGT | 51366 |
rs541283982 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102253722 | ATATTAGTGATATCA[C/T]TTAATATCCTAGAGC | 51366 |
rs541300994 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102297751 | ATATACAAAGATGAC[A/T]TGCAAAGAAATCTAA | 51366 |
rs541350537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102349062 | TAAGAACTGCCCAAG[A/G]TAACTTTGGAGAAAA | 51366 |
rs541354794 | snp | C/G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102282142 | CCACTGCACTCCGGC[C/G/T]TGGGCAACAGAGCGA | 51366 |
rs541355483 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102252864 | GCCAGAAATCCTACA[A/G]AGGAACTGAAAGGAG | 51366 |
rs541365939 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102372660 | TTTAGTTGAAACTGT[C/G]AAAAAGATTTCTATT | 51366 |
rs541383742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102364363 | ATTTTTGTATTTTTT[A/G]TAGAGACAGCGTTTT | 51366 |
rs541385812 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102395671 | CTATAAAATAAAATC[C/T]TAAAATCGTCCTTGG | 51366 |
rs541393980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102305877 | CGCCTCAGCCTCCCA[C/T]GTAGCTAGCATGCAC | 51366 |
rs541396831 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102398638 | ATACAAAAATTAGCC[A/G]GGCATGGTGGTGGGC | 51366 |
rs541397737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102312699 | GAGAAAACTGACCCA[C/T]ACAGCCAGTGATTAC | 51366 |
rs541453500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102338455 | TGCATGATCTGTATC[C/T]TTTTGGTCTGTGTCC | 51366 |
rs541453863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102405750 | CTTGAACCCGGGAGG[C/T]GGAGGTTGCAGTGAG | 51366 |
rs541462864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102397792 | AATCATGGACAATCA[C/T]AGATTCACAGTTCTT | 51366 |
rs541466284 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102274016 | AGAGGAAAAACGAAT[C/T]CCTAAAATCTGAAAG | 51366 |
rs541524205 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102404767 | ACAAAATTAGCCAGG[A/C]GTGGTGGCTCACACC | 51366 |
rs541548642 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102354783 | AAAAAACATTAAATG[C/G]ATCAGTATGTATTCC | 51366 |
rs541549920 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102304332 | AACTAACACTTCAGA[A/C]AGACTGAACTATCTG | 51366 |
rs541583652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102275030 | TCTGTGACAGGAAAT[A/G]CCCAAGATGAAACAT | 51366 |
rs541610131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102377645 | CAGGAGGCAGAGGTC[A/G]CAGCGAGCAGAGATC | 51366 |
rs541646618 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102332980 | AATCCTGAACAAACC[A/C]GCCCAATAGCAAGAG | 51366 |
rs541720550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102348176 | AGGTAGCAGCGAGCC[A/G]AGATCGCGCCACTGC | 51366 |
rs541723245 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102356518 | TAATCCCAGCACTTT[A/G]GGAGGCCGAGGCAGT | 51366 |
rs541744514 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102373822 | TTGCCGTTTTATTAA[C/T]GTCAAAGATGAAATC | 51366 |
rs541753504 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102261701 | GCAAGACTCCATCTC[A/T]CACACACACACACAC | 51366 |
rs541801774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102333100 | CAATTACACCCCTAC[A/G]GGCCCTGAAAACCCA | 51366 |
rs541804597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102288063 | GACCATTTCACTATA[C/T]ATTCAAATGAGGTTT | 51366 |
rs541814071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102279868 | AAACTGGAGAATGCA[C/T]TATTTAGTCCCATTT | 51366 |
rs541821963 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102368584 | AAGCACATGTCACCA[C/T]ACCAGGCTAATTTTT | 51366 |
rs541822674 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102340079 | GACTAATCACCACCT[A/C/G]TCTCCTGCACTAAAC | 51366 |
rs541830710 | snp | A/T | 6.58924e-05 | 0.0057395 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311388 | CACCCATTCCAAGAC[A/T]ACTAATAGGTGGAAG | 51366 |
rs541833826 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102391376 | ACATTTTGAGGACAG[C/G]TGGAGAAAAATGAAT | 51366 |
rs541849260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102286806 | CTGTGGCTCAGGCAG[A/G]ACTGCAGTGGCACCA | 51366 |
rs541861439 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303895 | TCTAATTTGTTATCA[G/T]ATTATTTTTCCCAGG | 51366 |
rs541872017 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102397344 | AGGCCAGCCATCTTT[C/G]TATTCCAGTGTATAC | 51366 |
rs541891935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102279423 | GTAAGTTTTATGTTA[C/T]GTGCAAATTTTACGT | 51366 |
rs541900658 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBR5 | GRCh38.p7 | 8:102346648 | TAATTCCAGCTACTC[A/G]GGAGGCTGAGGCATG | 51366 |
rs541910798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102354094 | GTACATAACATGTAT[A/G]CACACACAAGTCTGA | 51366 |
rs541948134 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102369509 | CAGTAATGGGTACAA[C/G]TTTCCCAAAATTCTA | 51366 |
rs541955519 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102390039 | GTTGGGATTACAGGC[A/G]TGAGCCACCACGCCC | 51366 |
rs541970209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102369696 | TTCCATGAAGAAAGG[A/G]GCTTGTTTTAAAACG | 51366 |
rs541973368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102294386 | GAACAATACCAAATA[C/T]ATGAAATCAGAAGAA | 51366 |
rs541976324 | in-del | -/ACC | 0.00716266 | 0.059414 | intron-variant | UBR5 | GRCh38.p7 | 8:102368254 | TTCATCTCACAGTTG[-/ACC]ACCACAGGAAACTTA | 51366 |
rs541979660 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102310616 | TGCCTCCCAAAGTAC[C/T]GGGATTACAAGCGTG | 51366 |
rs542006052 | in-del | -/GA | 0.00755907 | 0.0610114 | intron-variant | UBR5 | GRCh38.p7 | 8:102333078 | CGGTGATAAGGCCTG[-/GA]TGAGCCAATTACACC | 51366 |
rs542024953 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102357511 | TCAAGGTTATAGTGA[A/G]TTATCATTGTGCCAC | 51366 |
rs542027063 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102300563 | ATACTGATTAGCACA[A/G]AACCAGTATTGTTCA | 51366 |
rs542027656 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102274502 | TTTGGGAGGCCAAGG[C/G]AGGTGGATTACTTGA | 51366 |
rs542028119 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102282192 | AACAAACAAACAAAC[A/G]AACACCCAGATATAC | 51366 |
rs542033812 | in-del | -/CT | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102305783 | TGAGACAGTGTCTCA[-/CT]CTGTCTTCCAGGCTG | 51366 |
rs542106095 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102317114 | CACCGTGCACCAGCC[A/G]AAGCAGGGCGAGGCA | 51366 |
rs542108622 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102313444 | TCAGTACTCTGGAAG[A/G]ATTTTAAATGTCATG | 51366 |
rs542115968 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102281794 | TCACCTGGAGGGCTT[A/G]TTAAAACAGACCTCT | 51366 |
rs542122473 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102323704 | AGGCGTGGTGGCTCA[C/T]GCCTGTTATCCCAGC | 51366 |
rs542156348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102375219 | TACAAAAATTAGTCA[A/G]GGGTGGTGGTGCACA | 51366 |
rs542163194 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303921 | CCAGGGTGTTATTGG[A/G]AGGAACAAAAATGAA | 51366 |
rs542170999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102384579 | GGTGGTACATGCCTA[C/T]AGTCACAGCTACTTG | 51366 |
rs542179628 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102358796 | TTTTTTTTGAGACGG[C/G]GGTCTCTCATTTCCA | 51366 |
rs542181707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102366330 | TAATTTCCTTCCTAC[A/G]GAAGTCTACAAATTC | 51366 |
rs542184692 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102322951 | GTTGTGGGGTGGGGG[A/G]AGGGGGAGGGATAGC | 51366 |
rs542196655 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102375656 | CAATCTTCTTTCTCC[G/T]CTCCCTCTCCCTCCC | 51366 |
rs542232829 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102382346 | ATAGTGGGCCACAGT[A/T]ACAGAATACAGTGTA | 51366 |
rs542293408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102365531 | TCATTCAAGGATAGA[C/T]AGGTAGACAGGTGAA | 51366 |
rs542294317 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102365381 | GAGGCAGGAGAATCG[C/T]TTGAACCCGGGAGGC | 51366 |
rs542298922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102408868 | CAGAAGACCCATCAG[A/G]TGGACCTCAGCTGTC | 51366 |
rs542298976 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102330340 | TTGGTCAGATGGTAA[C/T]GTTATAGTGCTAAAA | 51366 |
rs542352699 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102365153 | AAACAATTTTAAGAA[A/T]ACAGCATGACATTAG | 51366 |
rs542360644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102336853 | TTACAAATTTTAGGA[C/T]TGCTTTTTTATTTCT | 51366 |
rs542364100 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102270919 | GAATATAATTTCAAC[C/G]GCCTCTGGGTTTTTA | 51366 |
rs542407508 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102360834 | ATATGACATACATAA[C/G]ATTATCAAGAAACCA | 51366 |
rs542416053 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102396030 | AAATAAAATCAAATA[A/T]AGGGGGAAGGGGTGG | 51366 |
rs542446871 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102407336 | GGTTTCACCATGTTG[C/G]CCAGGCTAAGGGGTC | 51366 |
rs542473320 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102257406 | ATCTTCTGGGACTAA[C/G]GACAGCATATTAACA | 51366 |
rs542478028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102265501 | TAACGTCTCTGTTGT[C/T]AAAATAAAGTCATTT | 51366 |
rs542492264 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102261718 | ACACACACACACACA[A/C]AAAGTACAAGCCCTT | 51366 |
rs542517888 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102360280 | AATTTGGAAATGATC[G/T]ATAAAATCATTTCAG | 51366 |
rs542559277 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102256667 | ACTAGGTGGCAGTTA[A/G]GACTGCTGAACAAAC | 51366 |
rs542578908 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102300452 | ATAATCTTTCATACA[C/G]TTCAGATAAAAGAAC | 51366 |
rs542582820 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102355980 | TTCTACCATCCTACT[C/T]TAGTCATTCTGTCAT | 51366 |
rs542586751 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102409379 | GACATCAGACTATGA[G/T]GCTGAACAAAATATT | 51366 |
rs542606284 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102315936 | TATTCTATTCTAATC[C/T]TGTATTTGTACACAT | 51366 |
rs542606572 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102308926 | AAGCCTAAAAGTTTT[C/T]TTTTTAAAAAAAAAA | 51366 |
rs542649995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102307907 | CCTAACATTTAAATG[C/T]TGAGACTATTCTCAG | 51366 |
rs542670821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102321040 | CACAAGACAGGGATG[C/T]CCTCTCTCACCACTC | 51366 |
rs542672999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102271591 | ACTAGACTCATTTAA[A/G]TATCCTCTGTTCTTA | 51366 |
rs542677163 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102268564 | ATGTAATCTGTTAGA[C/T]ATTTTTTAGATTTTA | 51366 |
rs542694081 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102315421 | AAGAAAATAACTACA[C/G]CAACTAAACAGCATT | 51366 |
rs542732336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102307164 | CTTGGAGCAACAAAC[C/T]CTAAGTAGTGAGAAC | 51366 |
rs542748872 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102350311 | GAAGGATTCACACTT[A/C]ACAATTTCAAAGCAT | 51366 |
rs542749633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102277732 | GAGCGCGGTGGCTCA[C/T]GCCTGTAATCCTAGC | 51366 |
rs542761010 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102357108 | AGGACACCTCCTTTC[C/T]AGTAATAAAACAACA | 51366 |
rs542830607 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBR5 | GRCh38.p7 | 8:102320051 | AAGCAAGAGCAAACA[C/T]ATTCAAAAGCTAGCA | 51366 |
rs542850320 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102335795 | CTCAGGTGATCCACC[C/T]GCCTTGGCCTCCCAA | 51366 |
rs542892124 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102328293 | CAGTAAGACTCTGCC[C/T]CTAGAAAAAAGTTTT | 51366 |
rs542895617 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102352366 | CTTCATAGTTTCCTA[C/T]GAGTTTTAAAAACTA | 51366 |
rs542927746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102334790 | GCAGTCCCAGCCACT[C/T]GGGAGGCTGAAGCAG | 51366 |
rs542961043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102299205 | CTAGTATCAGTAATA[A/G]ATTAACTTCATCACA | 51366 |
rs542996781 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102290901 | GATCTTGGGTTTTTT[G/T]TTTTTTTTTTAAATT | 51366 |
rs543007263 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102282912 | CACACTGCTACTGAG[A/C]CTGTCTTCCTTTTTG | 51366 |
rs543010726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102378372 | AACCAGGTCGGGTGC[A/G]GTGGCTCACACCTGT | 51366 |
rs543018070 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102400482 | CCTGGCCTAGCACAC[G/T]TTTTGCACATGAGAA | 51366 |
rs543026689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102326877 | TTTATAATTAAATTT[C/T]ATGGGAAATTCATCA | 51366 |
rs543044384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102282326 | ATAATGGGCTTACAT[A/G]CAGAATAAAGAACTC | 51366 |
rs543054132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102393623 | TCAGGGGGACAGAGC[A/G]AAGTTTCTTTTAAGA | 51366 |
rs543061808 | in-del | -/ACG | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102384123 | CAAGCCTTTTTGAAA[-/ACG]ACACAGAACTTTCTA | 51366 |
rs543117155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102400059 | TACCATTGAAGGAAG[C/T]TGGGTGATGGATCCA | 51366 |
rs543131912 | snp | G/T | 1.64787e-05 | 0.00287038 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102289562 | ATGATGTAGGATGAC[G/T]GAGACTGACTGGAGC | 51366 |
rs543140880 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102266581 | TCTGCCCACCTCGGT[C/T]TCCCAAAGGGCTGGG | 51366 |
rs543182531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102329020 | TGAAAAGATGGAAAA[A/G]GAGCAAAAAAGAAAA | 51366 |
rs543186215 | in-del | -/ATCT | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102255032 | TAATTATTGGGGAAC[-/ATCT]ATCTATGCATCAAAA | 51366 |
rs543237247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102407159 | CTGTCGCCCAGGCTG[A/G]AGTGCAGTGGCGCGA | 51366 |
rs543246048 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102396495 | TACACAGTATCTTTC[A/G]GATACACAGTATCAC | 51366 |
rs543290751 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | UBR5 | GRCh38.p7 | 8:102284158 | GAGCTGATACCTACT[A/C]CTGAAAAAGGTCACT | 51366 |
rs543299402 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102318501 | GAGAATGGAACCAAG[C/T]TGGAAAACACTCTTC | 51366 |
rs543356040 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102276118 | AAGTCCAATGTCTAT[C/G]TCCATTTAGGTGACT | 51366 |
rs543358706 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102285040 | AGACTCCGTCTCAAA[A/C]AAACAAACAAACAAA | 51366 |
rs543370669 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102388025 | ATAAAACATGTGTAA[A/C]ACACACGCTCTTTTT | 51366 |
rs543375607 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102384707 | CTTTAAAAACCAAAA[A/G]AGCTCTGCTGAGCTG | 51366 |
rs543379579 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102387424 | ATTAACAAAAAGTTC[C/G]TGGTCAGGGGTGGTG | 51366 |
rs543389089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102267227 | GTATGATTCAAGATA[A/G]TGGACTAAAGGCTCC | 51366 |
rs543396446 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102275283 | AACCAAACTGCCAGA[G/T]AAAACTACTATTCTA | 51366 |
rs543435835 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102412742 | CCGCTCCGGAGCGGC[A/G]GGGGAGGGGCAAACG | 51366 |
rs543443471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102326093 | TAGTACCCGTAGAAG[C/T]CTAAAACCATCTCAG | 51366 |
rs543455568 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102333642 | CATATTGTGAAAAAG[C/T]TGGCATCTCTATTCC | 51366 |
rs543489391 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102369478 | ATGTTACTATCAATC[G/T]ACAGTGTCAAACTCA | 51366 |
rs543494945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102341122 | CCTAGATTAATAATA[C/T]GTGGTGGCCCTATTA | 51366 |
rs543496611 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102358653 | TATTTAGTATAGCTA[A/C]AGGATGTACTCAACT | 51366 |
rs543516841 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102274480 | CTCACACCTGTAATC[A/C]CAGCACTTTGGGAGG | 51366 |
rs543531534 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102409413 | CTTTTTAAGAGGATG[C/T]GGGTAAAGAAAGAAA | 51366 |
rs543538307 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102310778 | CTTATAATCCTCCTC[C/T]TCCTCCTCGCTTTCA | 51366 |
rs543538333 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102282447 | GCCAAGGTGGGTGGA[C/T]CACCTGAGGTCAGGG | 51366 |
rs543539539 | in-del | -/A | 0.0158469 | 0.0875917 | intron-variant | UBR5 | GRCh38.p7 | 8:102361285 | CTTAAATACAATTAG[-/A]AAAAAAAAAGTTGGC | 51366 |
rs543550911 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102376652 | AGGATTACAGGCGCC[C/T]GCTACCACACCTGGC | 51366 |
rs543552467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102368928 | AAACTACTGAAGACC[C/T]CAAAAATCTTTTGTT | 51366 |
rs543553724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102281593 | ATAAATATGCAAAAT[C/T]AGGAGCTGAGAATAT | 51366 |
rs543558133 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102340135 | AATATCCGATCTTGT[C/G]ATTAATATAGCCCCC | 51366 |
rs543576318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102332794 | ATTCTATGTAAATGT[C/T]TGTGTTCCCCACTGA | 51366 |
rs543579690 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102297383 | CCAAAGCTGAAAACT[C/G]TAAGTCTAGTGATAG | 51366 |
rs543581950 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102269769 | TAAATATAATGCACA[A/G]CAAATTCTTTAGCAT | 51366 |
rs543603002 | snp | A/G | 2.24338e-05 | 0.00334909 | intron-variant | UBR5 | GRCh38.p7 | 8:102297027 | AATAATTATAAGTAT[A/G]CATATATCTCATCAT | 51366 |
rs543609450 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102364221 | GGGTCTCACTCTGTC[A/G]CCCAGGCTGGAGTGC | 51366 |
rs543619843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102398539 | TGTAATCCCAGCACT[C/T]TGGGAGGCCAAGGAG | 51366 |
rs543642818 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102406621 | TATTGCTTTTAGGTA[A/G]CAATCTCAATAATCA | 51366 |
rs543677770 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBR5 | GRCh38.p7 | 8:102252701 | CAGCGTGTTATATAA[A/G]TTTTAAGTAATACAA | 51366 |
rs543680849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102398020 | CAAAATAGCCAAAGT[C/T]ATCCTGAGCAAAATA | 51366 |
rs543718179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102363535 | GCCTTTAGAAGACCC[C/T]AAGAAGCAGCAGGAG | 51366 |
rs543740194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102333078 | CGGTGATAAGGCCTG[A/G]ATGAGCCAATTACAC | 51366 |
rs543763151 | in-del | -/GAA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102373942 | AGCTTGGTGAGGTGT[-/GAA]GAAGAGTACGCTGTA | 51366 |
rs543835747 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102397702 | GAAACTCTACCACAA[A/G]CAAACAAAAAAAAAT | 51366 |
rs543845179 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102412058 | CCCCCGCACCCCACC[C/T]CAGCTGGCCGGCCGG | 51366 |
rs543861927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102390111 | ATTAATTTACATCTA[C/T]GAACTTCCTTCAACA | 51366 |
rs543895146 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102354038 | CCTGTCTCAAAAAAA[A/G]AAAAAAAAAACCCTA | 51366 |
rs543898738 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102254811 | ACTAAATGGTTTCTA[A/G]GAGCCTTTCTTGCAG | 51366 |
rs543920120 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102256282 | CACTCCAGCCTGAGC[A/G]ACAGAGTGAGACTCC | 51366 |
rs543922090 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102317225 | ACCTGGAAAATCGGG[C/G]CACTCCCACCTGAAT | 51366 |
rs543956345 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102375802 | GCCTATTATAGTGCA[C/G]AGCCTGGCTGTCTAA | 51366 |
rs543965582 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBR5 | GRCh38.p7 | 8:102334808 | GAGGCTGAAGCAGGA[A/G]AATGGCATGAACCCA | 51366 |
rs543983287 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102253259 | AAGTCAAAATTTTTA[C/T]GCACATAACCATGTC | 51366 |
rs544025819 | snp | A/G | 1.6918e-05 | 0.00290839 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102257635 | TTTTTAACTTACAAG[A/G]TCTTGTCGTTCTGTC | 51366 |
rs544036308 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102308705 | TACTTCTTCTATCTA[-/T]TTTTTTTTAAAGTTA | 51366 |
rs544036557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102384334 | TGTTTAAAATGTATA[C/T]GGGCAATTTTAATCA | 51366 |
rs544056586 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | UBR5 | GRCh38.p7 | 8:102348170 | AGGCAGAGGTAGCAG[C/T]GAGCCGAGATCGCGC | 51366 |
rs544104959 | snp | C/T | 4.47999e-05 | 0.00473264 | intron-variant | UBR5 | GRCh38.p7 | 8:102312088 | TTTCCTGAACAAGTA[C/T]TAATGGAATATAGGA | 51366 |
rs544115071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102337772 | TAGGCCTTGTAAAAT[A/G]TGTTTGGTTTAGATT | 51366 |
rs544115314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102346620 | TTAGCTGGGTGTGGT[A/G]GTGCACACCCATTAA | 51366 |
rs544116792 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102347724 | GCTCACTGCAACCTC[C/T]GCCTCTGCCTCCTGC | 51366 |
rs544130772 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102393495 | CAAAAAATTAGCCAC[A/G]CATGGTAGCACACGC | 51366 |
rs544163242 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102349385 | TTAGCCAGCCATGGT[G/T]GCACTCACGTGTAGT | 51366 |
rs544178190 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102294658 | ATTCCAGTAAGTGGT[C/T]AGGCTATAATTTGAT | 51366 |
rs544229186 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102293237 | GAGCCCCAAGTCATT[A/T]TCATACATATTAAAG | 51366 |
rs544234472 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102314936 | AGACAAGTATTTTCT[C/T]ATAAAAGAATGAATA | 51366 |
rs544238237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102396766 | ACTGGACTGCAGTGG[C/T]GCGATCTCGGCTCAC | 51366 |
rs544238576 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102403850 | AGATCTGTTGCAAAA[C/G]CACTGTTCTAAGCAA | 51366 |
rs544241128 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102346867 | AACCTCACCTTGTCC[C/T]GTTGTCTGACATTAA | 51366 |
rs544272560 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102332817 | CCCACTGAATTCCTT[G/T]TAGAAAGGCCAATAT | 51366 |
rs544273555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102310146 | TATATTTCTTCTCTA[C/T]CATCAACCATGCCCA | 51366 |
rs544316875 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102329576 | TGGCCCTGGCTCCCT[A/C]CATTAACTCACTCAC | 51366 |
rs544317733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102292724 | ACACAGCTTGATTTG[C/T]AACAGTTTTCAACAA | 51366 |
rs544331905 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102395774 | GTCTAATACACAGAA[A/C]AATGGGTTTCCTGGA | 51366 |
rs544361213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102265379 | AGTCAGGTAGGAAGA[A/G]CAACATAAATATTTA | 51366 |
rs544364638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102316760 | GGCAGGAAGTTAGGT[A/G]GAAATTTAAGATGAT | 51366 |
rs544377861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102335976 | ATAATAGCTATACCA[A/G]TCTAGTTCCCAACAG | 51366 |
rs544384506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102280616 | GAATCTGGGAAATGG[C/T]AGAGTGAACAGGTTT | 51366 |
rs544402674 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102364963 | AACTGAAGTTTTTTT[-/A]GTTTGCTAATTATTC | 51366 |
rs544416179 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102378547 | TACCAGGGAGGCTGA[A/G]GCAGGAAAATCACTT | 51366 |
rs544445390 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | UBR5 | GRCh38.p7 | 8:102359810 | AAATGAAATAAATGG[C/T]GTGACATTATAAACA | 51366 |
rs544540964 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102263729 | CTCTATTTTTTTTTT[A/G]TTTTGTTTTATGAGA | 51366 |
rs544554012 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102381552 | GATACTGACAGTTCA[A/C]GCAGACAAAATTATC | 51366 |
rs544580017 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102270771 | TGATCCACCCACCTC[A/G]GCCTCCCAAAGTGCT | 51366 |
rs544590609 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102335794 | CCTCAGGTGATCCAC[C/T]CGCCTTGGCCTCCCA | 51366 |
rs544644087 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102365348 | TGCACGTCTGTAGTC[C/T]CAGCTACCCGGGAGG | 51366 |
rs544645881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102365028 | TCATACAATGTTTAC[A/G]ATAGGCAGTATTAAC | 51366 |
rs544667496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102269969 | ACAATTTTTTTTAAA[C/T]ACCATCTTTAATTCA | 51366 |
rs544684244 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102372827 | TGAAAAATACTCTGA[C/T]TAGAAATTCTTATAT | 51366 |
rs544716162 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102344917 | CTGGGCAACAGAGTG[A/C]GACTTCATCCCCAAA | 51366 |
rs544728370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102344178 | AGTAGTTTTACATTC[C/T]GGAAAGTAAAAATAT | 51366 |
rs544733010 | in-del | -/TGCAATGGCGCGATCTTGGCTTAC | 0.0562307 | 0.157967 | intron-variant | UBR5 | GRCh38.p7 | 8:102399326 | TCGCCCAGGCTAGAG[-/TGCAATGGCGCGATCTTGGCTTAC]TGCAATGGCGCGATC | 51366 |
rs544747957 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102371755 | GACCATGCCTGACTA[A/G]TTCTTGTATTTTTAG | 51366 |
rs544748024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102379775 | AGTAGAGATGATGCA[C/T]TGAGTTCACCCTGAG | 51366 |
rs544767944 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102328617 | TTTGAGACGGAGTCT[C/T]GCACTGTCACCTGCG | 51366 |
rs544784872 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102367733 | GAGCTACCTTGGCCT[A/G]TGAGGCTGGGAATGA | 51366 |
rs544803569 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102304742 | CTAAGTGATTTTTCT[C/T]CTCTACATTCTAAAA | 51366 |
rs544830501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102409600 | TATTTGTGACTCTCA[C/T]ACATTTCTCATAATA | 51366 |
rs544845749 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102299388 | AGATCTGTAGAACCC[C/T]ATATCCAAAGTGTGT | 51366 |
rs544872291 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102400865 | TACCCTATTCTCAAA[A/C]AGACAGGTATAAAAC | 51366 |
rs544914046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102330187 | ATCTCACAGCAAAAA[C/T]TGCCAGTAACGGATT | 51366 |
rs544937246 | snp | A/G | | | intron-variant, downstream-variant-500B, nc-transcript-variant | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102251877 | ATCAGAAAGGAGGCA[A/G]GAGGATGAGGAATGC | 51366 |
rs544960978 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102332514 | TCTCCTACTCCCCAC[C/G]ACAAAGCAGCAATTC | 51366 |
rs544963838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102374632 | CGTAGGTAGGTAGGT[A/G]ACATACAGATATTAG | 51366 |
rs544978980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102357755 | GTAAAACATTAACAC[A/G]GAAGCTGGGTGCAAC | 51366 |
rs545070036 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102319839 | TGCTCCTGAATGACT[A/G]CTGGGTACATAACGA | 51366 |
rs545090303 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102284630 | TCTAAACATGCAAGT[A/T]TAGATACTCCTTGAC | 51366 |
rs545108139 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102357935 | TGGATCACCTGAGGT[C/T]CGGAGTTCAAGACCA | 51366 |
rs545123209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102261766 | ACTAACTCTTGATCC[A/G]TCTTTAACACCGACA | 51366 |
rs545151414 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | UBR5 | GRCh38.p7 | 8:102312781 | TGAAATCCTCCCATC[A/T]CCTAATTAAATTAAA | 51366 |
rs545154784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102379137 | AGCTACCTCCTCTCT[C/T]GGTTTCTGAAAGGGG | 51366 |
rs545195892 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102351863 | TTGTGCGCCTACAGT[A/C/G]CCAGCTACTTAGAAG | 51366 |
rs545215139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102363435 | AAGGGTAATGTATTG[C/T]GGAACCCATGAGCTC | 51366 |
rs545229844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102308815 | GTAAAAAATTTTAAA[C/T]ATAGAAAAAGTGCTT | 51366 |
rs545262139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102283931 | TTTTGGTCTTCACTG[C/T]CCTACTTTAGTAACT | 51366 |
rs545262680 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102408800 | GACAGCAGAACCATT[C/G]TGGAATACAAGCCAC | 51366 |
rs545270853 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102358759 | TATCCCCCCCACAAC[C/G]CTTTTCTTTTCTTTT | 51366 |
rs545290839 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102386715 | GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 51366 |
rs545302254 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102315246 | ACTGAAAAAAAAAAA[C/G]GGTAAAGGCAAGTAA | 51366 |
rs545308342 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102351204 | ATATATTCGAAAGAA[C/T]TGAAACCAGGGTCTT | 51366 |
rs545309126 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102334743 | TCTACCAAAAATACA[A/C]AAGACTTAACCGGGC | 51366 |
rs545375612 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102342112 | CTTTAGAAATTTGAC[A/G]AAACAAATTTCTACC | 51366 |
rs545394614 | in-del | -/T | 0.0142736 | 0.0832652 | intron-variant | UBR5 | GRCh38.p7 | 8:102403680 | TGAAATAAGTACTAC[-/T]TTTTTTTGTTTGTTT | 51366 |
rs545412073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102393572 | ACCTGGGAGGTGGAG[A/G]TTGCAATGAGCTGAG | 51366 |
rs545416574 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102399989 | TGCACATGGGGAAAA[C/T]GTCTCTATCTCTAGT | 51366 |
rs545427117 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102399319 | TCACTCTGTCGCCCA[A/G]GCTAGAGTGCAATGG | 51366 |
rs545480056 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102289376 | TAGTCTCAAGCTACT[A/T]TTAATGTAATTTCTA | 51366 |
rs545509055 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102296262 | TCTTTTAATATCTAT[C/T]AAAATTTTTCATTTG | 51366 |
rs545514252 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102340094 | GTCTCCTGCACTAAA[A/C]CTCACAAGTTTCATA | 51366 |
rs545547016 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102398507 | GCTTCTGCAGGCTGG[G/T]CGTGGTGGCTCATGC | 51366 |
rs545560128 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102318468 | CTACGTCTGATTGGT[G/T]TACCTGAAAGTGATG | 51366 |
rs545568383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102268664 | TAAAAGAAATGTCAT[A/G]GTTATGGCAAGAACA | 51366 |
rs545596823 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102317720 | GACACCTCACACGGC[C/T]GGGTACTCCTCTGAG | 51366 |
rs545621797 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102356444 | ACAGAGGGAGACTCT[A/G]TCTCAAATTAGATAG | 51366 |
rs545644364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102290796 | AAACGCTACAAAAAA[C/T]TTAAAAAGAGTAATT | 51366 |
rs545664998 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102406882 | TTAAAACCTCAAAGT[C/T]CTTAATAAACATAAT | 51366 |
rs545667552 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102414051 | CTGGCAAGTTGCAGT[C/G]AGCTGAGATCATGCC | 51366 |
rs545695785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102341282 | GTTTAAATCAGTCCC[C/T]ACCATATGAAGTAAA | 51366 |
rs545697251 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102382778 | CCACAGATACATGAG[C/T]AGAGATTATGAGAAA | 51366 |
rs545730070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102290272 | AAGACCTTTAAGTGA[C/T]TGCACTGACAGGTTC | 51366 |
rs545757765 | in-del | -/ACAA | 0.00358779 | 0.0422022 | intron-variant | UBR5 | GRCh38.p7 | 8:102395434 | CCTGTTTACATATAC[-/ACAA]ACACAGTGTATTCAT | 51366 |
rs545773527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102281886 | AGCTCTTAGGTGAGG[C/T]TGATGGTGTTGTTCT | 51366 |
rs545776694 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102273919 | TGGTAAAAGAGACAA[C/G]AATGGACTTATATCC | 51366 |
rs545778568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102411444 | AGTAAAGGGAATCCA[A/G]TGCACTTCCCCACCC | 51366 |
rs545807783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102385367 | AAAATAATGTGAAGC[A/G]TGGAATCTATCAAAT | 51366 |
rs545812173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102288656 | GAGGCAAGATTGCAC[C/T]ACTGCATTCCAGCCT | 51366 |
rs545813458 | snp | G/T | 0 | 0 | intron-variant | UBR5 | GRCh38.p7 | 8:102375716 | GAAATGTGCTACAGG[G/T]ACCAAAAGGAAGCTG | 51366 |
rs545817466 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102404672 | CCAACACCCTGGGAG[C/G]CTAAGGCAGGTGAAC | 51366 |
rs545818770 | in-del | -/C | 0.00438332 | 0.0466095 | intron-variant | UBR5 | GRCh38.p7 | 8:102317349 | TGCTAGCACAGCACT[-/C]TGAGATCAAACCGCA | 51366 |
rs545820324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102333017 | GCATGAGGCCCTCTC[A/G]GAACTGACTTGCCTT | 51366 |
rs545882036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102339492 | CGAGATCACACCACT[A/G]TACTCCAACCTGGGC | 51366 |
rs545882558 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102335507 | GTATCCTATAACCTG[C/T]TGTAAACTTCAAATA | 51366 |
rs545894271 | snp | A/T | | | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102271157 | GTCCCTCCGAGAACC[A/T]GCTCGCAAACCACTA | 51366 |
rs545909286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102348091 | TTAGCTGGGCATGGT[A/G]CACGTGCCTGTAATC | 51366 |
rs545926157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102375331 | GTGTCCCTGGCACCC[C/T]AGCTTGGGCAACAGA | 51366 |
rs545987234 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102371380 | CTCCCCAGTAGCTGA[C/G]ACTATGGACGCATTC | 51366 |
rs545990656 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | UBR5 | GRCh38.p7 | 8:102299208 | GTATCAGTAATAAAT[C/T]AACTTCATCACAAAT | 51366 |
rs545992639 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102287811 | AGGGCAGTGCAGGGG[A/C]GGACTGAAAGTAAAT | 51366 |
rs546007639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102276046 | TCTGTATTCTACATA[C/T]GGATAAATCCCTGGG | 51366 |
rs546007642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102267996 | TCCCGGGTTTAAGCA[A/G]TTCTCCCTGCCTCAG | 51366 |
rs546025932 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102343888 | GCAGGGGGGAGAACA[C/T]GGGAAGAGACCTTTA | 51366 |
rs546026688 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102412916 | TTCGGCTCCCGAGCC[C/T]AGCCCCGCCGGGGGT | 51366 |
rs546038243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102378280 | GGATCCACCAGAAAA[C/T]GCTTCCAGTTCTTTG | 51366 |
rs546047470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102267105 | TACAAAATACATTCA[A/G]GTTTTGGAGTCAATA | 51366 |
rs546080077 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102337100 | TATTTGTGTATAGGA[A/C]TACTACTGATTTTTG | 51366 |
rs546091571 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102307888 | GCTCGTTCCTCTTTA[C/T]CACCCTAACATTTAA | 51366 |
rs546096902 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102369814 | CCTACAAGTACAAGA[A/G]AAGCAAAGAATACAA | 51366 |
rs546138629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102368847 | CCTCAGCAGCTTCCT[C/T]TCTTCACCTCTTACA | 51366 |
rs546149265 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | UBR5 | GRCh38.p7 | 8:102286915 | TGGGTGTGGTGGCAC[A/T]TGCCTATAATCCCAA | 51366 |
rs546149631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102377784 | TAGGCATTTTTATTC[C/T]TTTAAGTGTGAAAAT | 51366 |
rs546152371 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102319541 | TCAATGACACAGAAA[A/G]TTAACAAGGATACCC | 51366 |
rs546162774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102361855 | GTAACAATGATAATC[A/G]TATTAATCCCATTTT | 51366 |
rs546223912 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102369402 | TGGACCAGGATACAC[C/T]GGTCATTTGGAAAAC | 51366 |
rs546267489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102347408 | AGTAGCTGGGGATTA[C/T]AGGCACGCACTACCA | 51366 |
rs546276469 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102331917 | TCCCTGTATTCAAAT[C/T]GTGCTTCACCTTCAG | 51366 |
rs546319803 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102292337 | TATCACATGAGATCT[A/C]CTTCTGGGAAGATTT | 51366 |
rs546341628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102331132 | ACTACATATAACATA[C/T]AAAATATGTTGTTAA | 51366 |
rs546350197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102394721 | GGCTGGAGAGAGGTG[A/G]AGTACATTCTTTGTA | 51366 |
rs546355705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102381803 | ACAACTACTATTACT[A/G]ACATTTAAGAAAAGA | 51366 |
rs546366533 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBR5 | GRCh38.p7 | 8:102343828 | TGCACTCCAGCCTGA[A/G]CAACAAGAGCGAAAC | 51366 |
rs546373605 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102397950 | AAACACCAATGACAT[G/T]CTTCACAGAAATAGA | 51366 |
rs546388313 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102272221 | AATATTGAAGTGGAG[A/G]AAATGCTGCAATTTG | 51366 |
rs546425129 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102278525 | GTAGCCAAAATTACA[A/C]ATGCTCATCTATATA | 51366 |
rs546435577 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102284930 | TAGTCCCAGCTACTC[A/G]GGAGGCTGGGGCAGG | 51366 |
rs546457355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102310665 | ACATTAACCTTTTTA[C/T]CTGATCTCTAAACTT | 51366 |
rs546457776 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102381127 | CTGAGCACTTTGGGA[A/G]GCCAAGGCAGGTGTT | 51366 |
rs546494609 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102406606 | GCATAATGCATTTAG[C/T]ATTGCTTTTAGGTAA | 51366 |
rs546504004 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102311030 | ATCTGTCCGGGTATC[A/G]CTTCTTAAAGAAGTC | 51366 |
rs546514168 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102402331 | GGTTTGTAGAGGCAG[A/G]TGATGTTACAGAGCA | 51366 |
rs546520525 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102360943 | CTGTTACTAATTAGT[G/T]TCACACTCTGGCAAA | 51366 |
rs546573121 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102336912 | AGATTATGTATAAAT[A/C]TGTACATTACTTTGA | 51366 |
rs546616597 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102395367 | GCTGAATAAACACTC[C/T]TTTAATGATTTCACA | 51366 |
rs546621250 | snp | C/T | 1.64914e-05 | 0.00287149 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102327770 | TGTTTTCCAGCTGAG[C/T]GCAGGTGTAAAGGGC | 51366 |
rs546660469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102300595 | CACTAAATCCCTTTT[A/G]TAATCTCAAAAGCAT | 51366 |
rs546673429 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102372095 | CATATAAGAATTAAA[C/G]AATTGCTACAAGTTT | 51366 |
rs546681743 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102270543 | TTTTGCCAGACAGAA[-/T]TTTGCTCGTTTCCCA | 51366 |
rs546682710 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102334893 | ACAGAGCAAAACTCC[C/G]TCTCACCAAAAATAA | 51366 |
rs546696699 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102334511 | TGGCCAGACTGGTCT[C/T]GAACTCCTGACCTCA | 51366 |
rs546714995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102256123 | CCAGGCTAACATGGT[A/G]AAACCCTGTCTCTAC | 51366 |
rs546740313 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102372540 | CATTCACCTTCAAGA[A/T]GCATTCAAAGAAGAA | 51366 |
rs546745439 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102406826 | ATATAATCCCTGGCA[-/T]TATTTTCTGGCTCCT | 51366 |
rs546800343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102283388 | AAGAATGACTGCTAA[C/T]AGGTTTTCTGTAGAG | 51366 |
rs546813288 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102352178 | CCAGGTTTGGTGGTG[G/T]GTGCCTGTAGTCTCA | 51366 |
rs546850396 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102321457 | TACAAACAAATGGAA[G/T]AACATTCCATGCTCA | 51366 |
rs546863368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102400967 | TCAATCAATGTTAAG[A/G]CAAAGAAAAGAGGGT | 51366 |
rs546895738 | snp | C/T | 1.6651e-05 | 0.00288535 | intron-variant | UBR5 | GRCh38.p7 | 8:102285506 | AAACTTTTCAGTGGT[C/T]TCATACCTGTAAGTT | 51366 |
rs546903885 | in-del | -/AAAC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102269382 | TTATATCTCTGAGTT[-/AAAC]ATACATATACTCAAT | 51366 |
rs546935244 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102413365 | CACTAATTTCCTGAT[A/G]TAAATGATTCGTGAT | 51366 |
rs546946016 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102355745 | ATGGACCTAATGCTT[A/C]AAGAACGCTTACACA | 51366 |
rs546971602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102314079 | GGAGTTTTCTGATCA[A/G]TCTGTACTTCAAATA | 51366 |
rs546980353 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102385978 | CAAACACATAAAAGA[C/T]AGAAACAATTCAGTG | 51366 |
rs546997444 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102395025 | ACAGCAGTCTCTCAC[A/G]GTCTCCACATGTGCT | 51366 |
rs546998357 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102319265 | AGCAAATGGAAAACA[A/G]AAAAAGGCAGGGATT | 51366 |
rs547008153 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102380066 | AGGGAAAAAAAGGAG[A/T]GCAGAAAACTAACCA | 51366 |
rs547012570 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102364630 | ATACAGACATTTAGA[C/T]TGCTTCCCCAAATAT | 51366 |
rs547014085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102276870 | TTATTCAGTTTCCCC[C/T]TAGCTGAGCTGCTAA | 51366 |
rs547055818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102261479 | AGGCCAAGGTGGGTG[A/G]ATCATGAGGTCAGGA | 51366 |
rs547091105 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102291132 | CCAACAGACTTGCTG[G/T]CACAATGAAGCACAA | 51366 |
rs547149001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102298555 | TTCCTGATTATAAAT[A/G]TTCATGATAAAACAA | 51366 |
rs547149548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102268258 | ATTTTTCGTAGAGAC[A/G]GGTTTCATCATGTTG | 51366 |
rs547170010 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102318056 | TCCAAAGGAACGCAG[C/T]TCCTCACCAGCAACG | 51366 |
rs547183435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102308403 | AAAAAGATACCTAGT[A/G]CAGTCATGTGCTGCA | 51366 |
rs547193116 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102365294 | ACATGGCTAAGCCTC[G/T]TTTCTATTAAAAATT | 51366 |
rs547201533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102408976 | AGGCTATTAGTGAGG[C/T]AGGCCTTTCAGCTCT | 51366 |
rs547207130 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102340551 | GGTATTTATCCTGCG[C/T]CCCTGTATAATACTT | 51366 |
rs547209457 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102370628 | ATACAACAAATTATT[C/G]ATAACTATAGTCACC | 51366 |
rs547237003 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102334142 | AAAGAGCTTAAACAA[C/G]GGGTCAAATGAAATG | 51366 |
rs547246777 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102341246 | GATGTACAAAAAGAA[A/G]AAAAAAGTAAAAGCC | 51366 |
rs547262936 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102408269 | ACTGTCTCAACTGTT[A/C]CTCCCTGACCTTGAG | 51366 |
rs547287352 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102270991 | TGTATTTTATTAACA[A/G]ACTATTCTTAGTTAC | 51366 |
rs547304883 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | UBR5 | GRCh38.p7 | 8:102406710 | TCTGGGGGGTTTTTT[A/T]ATTGATTTTTTTGTT | 51366 |
rs547322469 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102363032 | AATTTTTGTAATTCA[A/G]TATAGATGGGGTTTC | 51366 |
rs547327504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102270246 | AGTAAAAATATTAGC[A/G]CAACTAGTAAAAAAG | 51366 |
rs547329445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102277402 | TTTTTTTTTTTAGAC[A/G]GAGTCTTGCTCTGTT | 51366 |
rs547332995 | in-del | -/AC | 0.00438332 | 0.0466095 | intron-variant | UBR5 | GRCh38.p7 | 8:102352289 | ACTCCAGCCTGGGTG[-/AC]AGAGTGAGACTCTGT | 51366 |
rs547339437 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102312993 | AGTGGCTACAATACA[C/T]TCAACACAGGGATAG | 51366 |
rs547361737 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102349582 | AAAGGGGGAAAGAGG[A/C]CAGGAAGGGAGAGAG | 51366 |
rs547390413 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102283347 | GGGGAAGGCGGGGGG[-/A]GGGGGGGGGTGAGTA | 51366 |
rs547439382 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102362921 | CAATGGTGCGATCTC[A/G]GCTCACTACAACCTC | 51366 |
rs547460699 | in-del | -/G | 0.000269937 | 0.0116145 | intron-variant | UBR5 | GRCh38.p7 | 8:102275854 | TTTAAGGGAAGGGGT[-/G]GGGGGGAGAAATAAT | 51366 |
rs547472351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102354992 | AATTAGCAGGGTGTG[A/G]TGGGGCATGCCTGTA | 51366 |
rs547529024 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102359970 | TTTTCTCACTCCATC[A/G]CTAGATAGAATATTG | 51366 |
rs547534946 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102326224 | ATATGAATCACCCGG[C/G]ATGTTTGTTAAACAC | 51366 |
rs547542235 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102350395 | AGACCAATGAAACAA[A/C]ATGGAACCCAGAAAT | 51366 |
rs547548698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102393732 | GCCAGGAGTTCGAGA[C/T]CAGCCTGGCCAGCAT | 51366 |
rs547589882 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102385553 | TTTTTTTTTTTTTGA[A/G]ACAGGTCTCACTGTG | 51366 |
rs547611584 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102400082 | TGGATCCATGGTACC[A/C]CTCTGTACCAATTTT | 51366 |
rs547620382 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102281994 | GGCAACATGGTGAAA[A/C]CCTGTCTCTACTAAA | 51366 |
rs547653239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102392112 | ATCCCTATTATTAAG[A/G]TCAAAAAATAACATT | 51366 |
rs547665959 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102377955 | ATCAAACCACTTGAC[A/C]ACCTCATTTTTTACT | 51366 |
rs547678499 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102272985 | TAAATCAGGACAACA[A/G]AATTTAATTCAATTC | 51366 |
rs547694363 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102388653 | TGAGTAGGTTTTACA[A/G]AATACTATTTCATAG | 51366 |
rs547710360 | snp | A/G | 5.25795e-05 | 0.00512708 | intron-variant | UBR5 | GRCh38.p7 | 8:102261898 | GCCAGAATCAGAAAA[A/G]TGTATATTTGCTTTA | 51366 |
rs547730724 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102383445 | GAAAAAGTGAAAGCT[A/G]TCTGCTGAAATCAGT | 51366 |
rs547756044 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102253120 | GTCACACTTCACTTC[A/C]CCCATTTGTAAAATG | 51366 |
rs547774089 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102352083 | GAGGCTGAGATGGGC[A/G]GATCACTTGAGGTCA | 51366 |
rs547850459 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102354910 | GGGGCAGGCAGACTG[C/T]TCAAGGTCAGGAGTT | 51366 |
rs547851962 | snp | A/G | 1.65946e-05 | 0.00288046 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102347077 | ACTTCCACCCACTCC[A/G]GAACTCCAGCGGCTT | 51366 |
rs547856219 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102305357 | AGCACATTACATATA[A/T]TAAAAATTTCTCATG | 51366 |
rs547873234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102337895 | AATAAATTGCAAAAA[C/T]GACTGAGAAGAGAAA | 51366 |
rs547923999 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102412155 | CCCCCGCGCCCGCCG[A/C]CCCGCCAGCCCTATT | 51366 |
rs547942361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102381970 | AACTTTTTTGATCTC[A/G]GGAAAAAGAAACATA | 51366 |
rs547974174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102292935 | GGGAACTATCCCAAA[C/T]ACTAAAGCAGGCCAT | 51366 |
rs547978407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102377363 | AATCAACTGAAAGGA[C/T]TTTTTAAAGAGCATA | 51366 |
rs548063941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102266569 | CTGATCTCGTGATCT[A/G]CCCACCTCGGTCTCC | 51366 |
rs548097598 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102332276 | TCACAATTTCCTTGA[A/G]CAACTGTAGCATTCT | 51366 |
rs548141318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102324178 | TTTAAAAAGTAAAAT[A/G]TGAAAAAAAAAATTA | 51366 |
rs548150491 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102316258 | CATAACATCTGAGTA[C/T]AAATGGAAAGCAAAC | 51366 |
rs548173118 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102345791 | CTTGTGGCCGGGCAC[A/G]GTGGCTCACATCTGT | 51366 |
rs548182649 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102263545 | AGCAAACGGTTTTTC[-/T]TTTCCCCCTGCCATC | 51366 |
rs548203235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102280112 | TGTAATAAGAGTATA[C/T]TAAGAGTAAAGGTAA | 51366 |
rs548211338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102383052 | ACGAGGCTAGTGCAT[C/T]CAACAAATTTTGGAA | 51366 |
rs548234031 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102316129 | AGGTATAAAGTGCAA[C/T]AGCTTTGGTTTGTTA | 51366 |
rs548270825 | snp | C/T | 6.59783e-05 | 0.00574324 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102272736 | TGTTAAGCTGCCTCA[C/T]AGTCTGCTGAATGAG | 51366 |
rs548273944 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102396897 | ATTTTTAGTAGAGAC[A/G]GAGTTTCACTTTGTT | 51366 |
rs548285596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102278316 | ACACAGACATTCCCA[C/T]GTGAAATTTACTTAC | 51366 |
rs548334527 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102322457 | AGGTGCTGGAGAGGA[A/T]GTGGAGAAATAGGAA | 51366 |
rs548339607 | snp | A/G | 0.000461856 | 0.0151893 | intron-variant | UBR5 | GRCh38.p7 | 8:102266899 | TATTGAAATTTCCTT[A/G]TAATTTAAATTCTGT | 51366 |
rs548400493 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102271341 | TGAGACAAATGTAAG[A/G]AAACATGACAGCTAA | 51366 |
rs548410701 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102320640 | GAGACACTACCAAAA[A/C]ACAGAATTTTAGACC | 51366 |
rs548455857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102309682 | TACAGAAATACACTA[C/T]ATAGGTTTATACCCT | 51366 |
rs548459486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102317040 | CATTTCCATTTGAGG[C/T]ACCGGGTTCATCTCA | 51366 |
rs548475979 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102288544 | GACTCTACTAAAAAT[A/G]CAAAAATTAGCTGGG | 51366 |
rs548482186 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102414189 | TTCTCAAAGGTTTCT[A/G]TGACCTCCTTTAAAA | 51366 |
rs548483282 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102323213 | TGTTAGGAGTTTACA[A/G]CTTCACACCTCTAAG | 51366 |
rs548510471 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102280892 | CGCCTGTAAGTCCTA[C/T]ATACTTAGAAGGCTA | 51366 |
rs548539977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102298695 | CTCTTTCACTCAACA[A/G]AGCTTAGCAGTAGAG | 51366 |
rs548545994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102394533 | CCACAGTTAATATCA[C/T]AGACTTTTTCACCTC | 51366 |
rs548552329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102256065 | AACGGCAGAATTGGG[A/G]GGCCAAGACAGGCGG | 51366 |
rs548552762 | in-del | -/A | 0.0189856 | 0.0955633 | intron-variant | UBR5 | GRCh38.p7 | 8:102260041 | AAAAAAAAAAATATT[-/A]TTTTTTTACCCTGGA | 51366 |
rs548552827 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102293110 | ACAGCATTATTACTG[-/A]AAAGTCTGACCCCTA | 51366 |
rs548562551 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102359113 | ACCTACCAATTTGTG[C/G]TCTGGAGGGAAAAAA | 51366 |
rs548564563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102366740 | TCCACTCATGGAATA[A/G]AACTTTTACATACCC | 51366 |
rs548572225 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102283190 | GAATGAAGTACTGAT[A/G]TATGCTAAATATAGA | 51366 |
rs548627775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102365965 | CTCTGCCTAACTCTA[A/G]CATATAACATATCTG | 51366 |
rs548631060 | snp | C/T | | | intron-variant, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102258371 | TTCACAGAGAACTTC[C/T]TGGAGCTTCTAATGT | 51366 |
rs548633337 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102271996 | GCTAAGAGTCCTAAC[C/G]CCAAAGTGTTGATCC | 51366 |
rs548636453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102263513 | GCTGCATAATTAGCA[C/T]TGTATATTAATTTTA | 51366 |
rs548649281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102352212 | ACTTGGGGGGACTGA[A/G]GCAGGAGAATCACTT | 51366 |
rs548655098 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102297106 | AATTAATGTGCTTTG[A/G]AAAACTAGAACTTAT | 51366 |
rs548664138 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102291351 | TGTATAAAGCTTGGA[C/G]AGACAAGTGCCACCA | 51366 |
rs548675436 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102262731 | TCTGATTAAAGAGAA[A/T]TATTAGGAGGCTACA | 51366 |
rs548698663 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102374145 | TATACCTTGGAAAGA[A/G]CAGGCACTTAAGTGT | 51366 |
rs548708893 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102269629 | TAAAGAAAAACTCTT[C/G]ATAGAACATTCAAAA | 51366 |
rs548735615 | snp | A/G | 8.66288e-05 | 0.0065808 | intron-variant | UBR5 | GRCh38.p7 | 8:102345389 | ATATAAATAAATGCA[A/G]AATTACCTCGAGATG | 51366 |
rs548751321 | snp | C/T | 3.32381e-05 | 0.00407651 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102298866 | GCAGAAAGAAGTTCT[C/T]GTAGATAGGGCTGGA | 51366 |
rs548753377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102400294 | TGTCTCAAAAAAAAA[A/G]AAAGGTAGAAAAACA | 51366 |
rs548760860 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102277689 | CCAGCCTTACCCACC[A/C]CCCTCCTTTAAATTC | 51366 |
rs548761057 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102405875 | GGAGACATTAAGTAC[A/G]TCCTCCTGTAACATA | 51366 |
rs548781740 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102350551 | GAACCCTTATCTTAC[A/T]TTATATACAAAAATT | 51366 |
rs548796607 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102383694 | GATGGGGAGGGAAAA[G/T]TATTAAAGAAATAAC | 51366 |
rs548798394 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102284863 | AACACAGTGAAACCC[A/C]GTCTCTACTAAGAAA | 51366 |
rs548808049 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | UBR5 | GRCh38.p7 | 8:102302388 | TATTTTCTGACAATA[C/T]GGAAGAATTCAAGGA | 51366 |
rs548819996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102402432 | ATCAGCTGAACAATC[C/T]AATACCCCTCTCCCC | 51366 |
rs548822809 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102407521 | TGTAATCCCAGCATT[G/T]TGGTAGGCTGAGGCA | 51366 |
rs548831129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102387972 | AGAAGGCTTTCAGAT[A/G]TAAGGCCTCTTTTGA | 51366 |
rs548843322 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102357311 | AGACTGAGGATCTGG[C/T]CCAGATTAGAGGAAA | 51366 |
rs548848746 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102352920 | CAGTTTACAATCTCT[A/G]CTACACAAGCCCTCC | 51366 |
rs548856329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102257832 | CATTATTTAAGACTT[A/G]GGGGGGAGCGTCTAA | 51366 |
rs548926233 | snp | A/G | 0.000350114 | 0.0132263 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102299519 | AAGAGATCCCACAGC[A/G]GGGGCCAGGATAAAA | 51366 |
rs548937009 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102328733 | CTGGTATTACAGGCG[A/C]CTGCCACCACACCCA | 51366 |
rs548941229 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102292790 | GAGAGCTCTGTCAGA[C/G]AAAACTGGATTTAGA | 51366 |
rs548941765 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102257104 | ACTTGATGGGTGGAC[C/G]TAAGTTCCACTAAGA | 51366 |
rs548947848 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102359857 | ACATTTTTTAAAGGT[C/G]AAGAGCCTAGATTAA | 51366 |
rs549001798 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102400942 | GCAAGTTTGGCCCTA[G/T]TTGCCATCATCAATC | 51366 |
rs549018214 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102408126 | ATGCTAAGGATATTC[C/G/T]AGGGCAACTCTTTTG | 51366 |
rs549056329 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102375903 | ACTGGAGGTCTTCCA[A/G]TGGCAAGTAATACAA | 51366 |
rs549056819 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102334096 | ATAACCCACAAGTCT[G/T]ATCAGCTGGTTCCAA | 51366 |
rs549071198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102340685 | ACTGATCACTATGAT[A/G]ATGCTTAACAGTTTA | 51366 |
rs549149859 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102380967 | TCCACATGGCTGGGG[A/G]AGCCTCAGGAAACTT | 51366 |
rs549179077 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102372004 | TCCAGGAGTTTGAGG[G/T]AAAAGTGAGCTATGA | 51366 |
rs549186375 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | UBR5 | GRCh38.p7 | 8:102409759 | TTTTGGAAACAGATT[C/T]TTCTCAAGTGACAGG | 51366 |
rs549189449 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102364112 | GGTCTCAAGTTCTCA[A/T]CTATGTGAGGAAGAA | 51366 |
rs549209824 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102319893 | TATTTGAAACCAACG[A/G]GAACAAAGACACAAC | 51366 |
rs549245174 | in-del | -/C | 0.00120361 | 0.0245022 | intron-variant | UBR5 | GRCh38.p7 | 8:102404214 | AGTACTTTAGCTGTG[-/C]CAAGTAACATAAATT | 51366 |
rs549289357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102335607 | AGGCTGTAGTGCAGT[A/G]GTGTGATCTTGGCAC | 51366 |
rs549365632 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102318686 | GTTAAGGGCAGCCAG[A/C]GAGAAAGGTCAGGTT | 51366 |
rs549376919 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102317586 | GCTTTGAAGAGAGCA[A/C/G]TAGTTCTCCCAGCGT | 51366 |
rs549381963 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102269183 | CTACAATCTTTTATT[A/T]AAAAAAAAAATAAAA | 51366 |
rs549392720 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102373191 | GTTATTTTCAGCTCC[A/G]TTCGAAACAGGAAAA | 51366 |
rs549419185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102276288 | CTCCTGATTTTTTTT[C/T]AGTAGTAACATCTCT | 51366 |
rs549428997 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102327159 | CTGGCCTTGGCCTCC[A/G]AAAGTGCTGGGCCTC | 51366 |
rs549456529 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102349284 | AACACTTTGGAAGGC[C/G]CAAGAGGGAGGATCA | 51366 |
rs549463767 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102393114 | TTTGCCTGTTTTCCT[G/T]ACTGATGTAGTCCAA | 51366 |
rs549478700 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102297881 | TGTTTCAGGCAGTTA[A/G]GACTCAACTCCTGGC | 51366 |
rs549519362 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102289828 | TGAGTCCATCCCATC[A/G]AAAAATTCTACAGGA | 51366 |
rs549543018 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102274606 | GCATGGTGGCAGACA[A/C]CTGTAATCCCAGCTA | 51366 |
rs549563573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102325538 | AGATAAACCTCAACC[A/G]GAATGTAATAAATTA | 51366 |
rs549570468 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102314059 | AAGCTACTGCTTTAT[G/T]AATTGGAGTTTTCTG | 51366 |
rs549589995 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102392809 | AGGCAACAATGAGCC[-/T]GTTATCAGGTCTCCC | 51366 |
rs549592769 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102380288 | AGTCCCAGCTACTCG[C/G]GAGATTGACACAGGA | 51366 |
rs549603213 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102350568 | TATATACAAAAATTA[A/G]CAAAAAATGAATTAA | 51366 |
rs549612133 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102309553 | TTCATTTGTGCTAAA[C/T]GCCCTATCAGGTGCA | 51366 |
rs549625135 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102333065 | GCAATGTCCCCCACG[G/T]TGATAAGGCCTGGAT | 51366 |
rs549670031 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102297312 | AACTGAGCAATCAGC[A/T]CTTTTGCCTCATTTA | 51366 |
rs549678027 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102348421 | TCAGCACTATCAACC[A/C]CCTTGTCCAAGAGAA | 51366 |
rs549686818 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102414368 | CAGACCTGGTACCCT[C/T]AAGGCAGATAATGGA | 51366 |
rs549687469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102379293 | ATGTTTGTAAAACGC[A/G]GTCGCCATCATCATA | 51366 |
rs549724497 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102294871 | TGTTATTACCATAAC[C/T]TCATTCGCACTGGAT | 51366 |
rs549750976 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102397497 | CAGGAGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 51366 |
rs549758030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102306129 | GGTACTGATAAGTAT[C/T]TATAGAACATATCAT | 51366 |
rs549763770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102406018 | AGGGGAAAAAACCCT[A/G]ACCTTTCCTAATTTC | 51366 |
rs549782993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102355804 | CAAAGAGGGGTTTAC[A/G]GGGAGTGTAAGAAAT | 51366 |
rs549796008 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102267591 | TCCAGAGACAGGGCA[C/G]AGGAATAAACGAACA | 51366 |
rs549823627 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102413052 | AGGAGGAAGAGGGGC[A/T]CTTGTGTTCTTTCGC | 51366 |
rs549835250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102259310 | AAAAGAGAGAAAGGC[A/G]GGAAGTGGGGAGGGA | 51366 |
rs549846502 | in-del | -/TAAG | | | utr-variant-3-prime | UBR5 | GRCh38.p7 | 8:102252697 | ATACAGCGTGTTATA[-/TAAG]TAAGTTTTAAGTAAT | 51366 |
rs549865274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102274277 | TGCCCAGGCTGTCCT[C/T]GAATTCCTGGACTCA | 51366 |
rs549874957 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102354377 | CCCACCTGAAGGGGG[A/C]CTTCAACTATTTGCA | 51366 |
rs549920780 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102410229 | AAAAATGAATCAAAG[C/T]GCCCAACACAACCGC | 51366 |
rs549954521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102404267 | ATTAAATATTAATAC[C/T]TTCTTTAATATCCTG | 51366 |
rs549985617 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102253062 | TCAAAACAAAAACCT[A/G]TCAGTTATTAGGTGT | 51366 |
rs550002614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102288374 | CAGTTTTGAAAATCT[C/T]CATTTGTTAGTGACA | 51366 |
rs550019260 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102252324 | TTTTATGATTTACTT[A/T]AAAAAAAAATCTTTT | 51366 |
rs550028269 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102355324 | AGTCTCTTTCATATT[A/G]CATTGTATTTGGTAA | 51366 |
rs550035272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102391070 | TCTACTTCAGAGGCC[A/G]AAGTGGGAGAATCTC | 51366 |
rs550039413 | snp | A/G | 1.65386e-05 | 0.00287559 | intron-variant | UBR5 | GRCh38.p7 | 8:102295612 | TTGATTTAACTTACT[A/G]TATGTTCTAAAAATC | 51366 |
rs550040635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102398777 | CAGAGCAAGACTCCA[C/T]CTCAAAAAATAAAAA | 51366 |
rs550053991 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102268080 | TTATTTACTTATTTA[G/T]TTTTTGAGATGGAGT | 51366 |
rs550066475 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102405558 | GAGCGCAGTGGCTCC[C/T]GCCTGTAATCCCAAC | 51366 |
rs550070400 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102363748 | GCCTTTTTCAAAACC[A/G]GACAATGCCTGAGAT | 51366 |
rs550167240 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102346177 | TTGTGCTTTAAATTC[C/T]ACTCCCCAGTCGAAA | 51366 |
rs550197219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303597 | ATGTGTTATAAAAGT[C/T]TGTCCATCCCAAAAC | 51366 |
rs550199883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102310807 | CAGGCTGAAGTTTAG[A/G]TAGCGTTAGGTGAAC | 51366 |
rs550223959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102353728 | CATGGGAACTCTCAG[C/T]ATGATGTTTGAAATT | 51366 |
rs550250089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102345230 | TCTAAAATACTATTG[C/T]GGCTCTTCAAAATAA | 51366 |
rs550262191 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102344655 | CATTTTAGGCTGGGC[A/G]CAGTGACTCATGCTT | 51366 |
rs550264721 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102410819 | GGCATCATGCAACTT[A/C]AGTCACCCGGTCACT | 51366 |
rs550304395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102281176 | TATGAAATGGTCCTG[C/T]GCTAGTTCTCTTTTG | 51366 |
rs550351371 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102339064 | TGGAACTTTCAAGAT[C/G]CCTATAATTTTCAAT | 51366 |
rs550352228 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102265017 | CACCCAGCGTACATA[C/T]ATTTTAAAACAAATA | 51366 |
rs550371833 | in-del | -/A | 0.00676609 | 0.0577691 | intron-variant | UBR5 | GRCh38.p7 | 8:102255100 | TCATACCTCTGTAAT[-/A]AAACTTTGTGCAACA | 51366 |
rs550376483 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102375380 | AAATAAAAATAAAAT[C/G]AATAAAAAATAAAAG | 51366 |
rs550376600 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102367166 | AGAACATGGTCCGCA[G/T]TTAAATTATCATGCA | 51366 |
rs550385429 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102376226 | TGCAAAAGTAATGTG[C/T]ACTCTCTAAAATAAG | 51366 |
rs550390625 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102304963 | CCTTCTGAGAAAGTA[-/A]AAAAAAAAAAAAAAA | 51366 |
rs550484457 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102338605 | TCCTGGGACAGGACC[A/T]TGCTTCTCCTTGCTC | 51366 |
rs550494223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102273615 | AAAAACACGAGGCCA[C/T]TCATCACACTATCTG | 51366 |
rs550496540 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102346819 | TCAGAACTCATGATA[A/T]GAGTCATGACTACAA | 51366 |
rs550502236 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102359974 | CTCACTCCATCACTA[C/G]ATAGAATATTGAAGA | 51366 |
rs550532823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102280063 | ATCTATTTTGCATCA[A/G]TATTAACAACGGTTT | 51366 |
rs550534253 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102286195 | AAGATGCAATAATGC[A/G]AAGACTGGGAAACCC | 51366 |
rs550543682 | in-del | -/A | 0.00716266 | 0.059414 | intron-variant | UBR5 | GRCh38.p7 | 8:102350375 | TATGGGCATAACGAC[-/A]AAAAAGACCAATGAA | 51366 |
rs550553212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102331407 | CTCAGGCAGGGGCTT[C/T]CTCAATATTCCTAGC | 51366 |
rs550585245 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBR5 | GRCh38.p7 | 8:102378719 | AACCTAATAACTCAA[C/T]GTACGCTGACTCAAC | 51366 |
rs550596514 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | UBR5 | GRCh38.p7 | 8:102352133 | GCCTACCTGGTGAAA[A/C]CCCAGCTCTACGAAA | 51366 |
rs550605095 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102266591 | TCGGTCTCCCAAAGG[A/G]CTGGGATTACAGGCG | 51366 |
rs550670734 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102396242 | GGCAGAACTGGCCAA[A/C]ATATATCAAATGTAA | 51366 |
rs550718208 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102394585 | CTTTTATTCAGCTCC[A/G]TGATTCTACTGGTTT | 51366 |
rs550769617 | in-del | -/GGAAATTAGCATAA | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102383234 | AAAACAGGAACTGTT[-/GGAAATTAGCATAA]GGAAATTAGCATAAG | 51366 |
rs550769696 | in-del | -/TAC | 0.000187559 | 0.00968216 | intron-variant | UBR5 | GRCh38.p7 | 8:102298525 | TGTAAAAATATTAAT[-/TAC]TACTTATTTTCCTTC | 51366 |
rs550780196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102272901 | AAAACAACAAAGTAA[C/T]TGGAGTTCTCAGAAG | 51366 |
rs550795083 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102301575 | AAAGATATCACCCAG[A/G]GGAAAAGGAAGACTC | 51366 |
rs550805414 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102266866 | CAGTTTCTTCAGAAA[A/T]CCTGCTTTCATCCCC | 51366 |
rs550805577 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102316470 | AATGTTATTTAACAA[C/T]TTTACTAAAGTTTTA | 51366 |
rs550806138 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | UBR5 | GRCh38.p7 | 8:102370391 | AGGCTGGTCTCGAAC[G/T]CCCGAACTCAGGTGA | 51366 |
rs550812213 | snp | A/C/T | 0.000115353 | 0.00759372 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102276980 | CAAATACCTGAAAGA[A/C/T]GTGAGAGGTGGCCCT | 51366 |
rs550831535 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102323113 | ATTAATTAATTAATT[A/T]ATAGATATATATTAG | 51366 |
rs550845579 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102322650 | GCACACGTATGTTTA[C/T]TGCGGCACTATTGAC | 51366 |
rs550864573 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102330589 | CAAACCATTACTGAC[G/T]TTCTCCATAGAAACT | 51366 |
rs550870515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102279619 | ACAAATCCAAACAGA[A/G]GAGATGATCAGGAAC | 51366 |
rs550879726 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102393122 | TTTTCCTGACTGATG[C/T]AGTCCAAGTGTCTGG | 51366 |
rs550886140 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | UBR5 | GRCh38.p7 | 8:102321256 | CTCAGGATACAAAAT[C/T]AATGTACAAAAATCA | 51366 |
rs550926721 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102298040 | TCTGTCAGAAATAAC[A/C]AGACATCTGTCTATT | 51366 |
rs550928636 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102290756 | ACAGGAATTTAAGAC[C/T]GACCTGGGCAACACA | 51366 |
rs550948079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102374017 | GCTCTGGAACTTTGG[C/T]AGAGCTTATTTTAAC | 51366 |
rs550953190 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102371425 | TTGGATATTCTCTGA[C/T]ACTACATCAAAACTC | 51366 |
rs550964850 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102259209 | ACAAGACATAATTTT[A/C]GCAGCCTTCTCTAAC | 51366 |
rs550965092 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102256163 | AAAAAATTAGCCAGG[C/T]GTGGTGGCAGGCACC | 51366 |
rs550973183 | in-del | -/G | 0.000269937 | 0.0116145 | intron-variant | UBR5 | GRCh38.p7 | 8:102275853 | TTTAAGGGAAGGGGT[-/G]GGGGGGGAGAAATAA | 51366 |
rs550979120 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102277595 | ATGTTGGCCAGTATG[G/T]TCTTGAACTCCTGAC | 51366 |
rs551006592 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102407451 | ATCTTAATTTAAACA[A/G]TCATGTTTTAAAAAT | 51366 |
rs551019091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102406818 | TTATGCTTCATATAA[C/T]CCCTGGCATATTTTC | 51366 |
rs551035376 | snp | A/G | 3.40541e-05 | 0.00412625 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102262065 | AGCAAAATCATGCCA[A/G]TTGACCTAAAAAAGT | 51366 |
rs551052602 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102328662 | TACGATCTCAGCTCA[C/T]TGCAACCTCCACCTC | 51366 |
rs551062021 | snp | C/T | 1.64787e-05 | 0.00287038 | intron-variant | UBR5 | GRCh38.p7 | 8:102268933 | CATACTGAAAGTAAG[C/T]AGCTGATGTTTAAAC | 51366 |
rs551088575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102272413 | AATCAATCTAGAATA[A/G]AAGTATGTAAAAATG | 51366 |
rs551106747 | in-del | -/GATTTTATACA | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102364609 | TGAAACTTTCAAATG[-/GATTTTATACA]GACATTTAGATTGCT | 51366 |
rs551119877 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBR5 | GRCh38.p7 | 8:102300826 | TCACTAAAAAGAAAA[A/G]GAAATAATCACAAAC | 51366 |
rs551128310 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBR5 | GRCh38.p7 | 8:102309110 | CAGGCTGGAGTGCAG[C/T]GGCATGATCTCAGCT | 51366 |
rs551129688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102380126 | AGGCCGGGCGCGGTG[A/G]CTCAGGCCTGTAATC | 51366 |
rs551144651 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102413984 | CAGGCATGGCTGTGC[A/G]CGCCTGTAAACCCCA | 51366 |
rs551167319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102356653 | TAGTCCCAGCTACTC[A/G]AGAGGCTGAGGCAGG | 51366 |
rs551170137 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | UBR5 | GRCh38.p7 | 8:102393202 | GAAACTTTAAGTCAA[-/T]TTTTTTTAAATGACT | 51366 |
rs551170146 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102354176 | TCCCAACATTTAAGA[-/T]TAAGAGATTATCACA | 51366 |
rs551199473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102291291 | ATTAAAAAAAAAAAA[A/G]AAAAAAAGGACAGCT | 51366 |
rs551201232 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102356878 | AATGATAATTTTTTT[-/A]AAAAAATCACCATTT | 51366 |
rs551206669 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102414236 | GAAGGCAAAAACTGA[A/G]AACATGACATTCCTT | 51366 |
rs551230981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102363905 | GGCTATCTGGGGAGA[C/T]AGCACAAATGGTTAC | 51366 |
rs551237528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102359039 | CCTTGGCCTCCCAAC[A/G]TGCTGAGAGGTGTAA | 51366 |
rs551276959 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102383945 | GAACTCCTCAAAAGG[C/G]ATACTGGAAGCTATG | 51366 |
rs551298117 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102263807 | GCCTCACTGAAGCCT[C/G]AAACTCCTGGGCTCA | 51366 |
rs551298811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102365786 | GGAAAACAGTGTAAC[A/G]GTACTTGCTAGAAGC | 51366 |
rs551299762 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102271893 | CCTACAAGTCTGATA[A/G]TCTTCTGCTCCTACT | 51366 |
rs551312968 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102334953 | AAAGTATCTGCACTC[A/T]CATATTCACTGTGGT | 51366 |
rs551321494 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102307473 | ATAAAAGCTTACAGA[G/T]AGTGCTCATAAGCAC | 51366 |
rs551323645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102357283 | TTCAAACTCATCATG[A/G]CCAGAAAGATAAAGA | 51366 |
rs551360166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102314002 | TTATAAGAAAGACTA[C/T]CTTTAAAGGGATACA | 51366 |
rs551446626 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102348237 | GTCTCAAAAATAAAT[A/T]AATTAATTAATTAAA | 51366 |
rs551458067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102340502 | AATTTTGAGAAACCA[A/G]TATAAGTCTCACATA | 51366 |
rs551490829 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102392269 | TTGGGGACTGCTCTG[C/T]CTATGGAGTAGCCAT | 51366 |
rs551504604 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102355765 | ACGCTTACACAGTCT[C/G/T]TTCTGGCAGAGAGAA | 51366 |
rs551528315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102318636 | CCAAGACACATAATT[A/G]TCAAATTCACCAAAG | 51366 |
rs551532400 | in-del | -/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102380399 | AAAAAAAAAAAAAAA[-/C]AAAAACAAAAACAAA | 51366 |
rs551550148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102387575 | CAAAAATTAGCCAGG[C/T]GTGGTAGCATGCACC | 51366 |
rs551560181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102394420 | CAGAAGTATATAAAA[C/T]ACAAAATCATATCAA | 51366 |
rs551574838 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102343579 | ACATTTGGCCAGGTA[C/T]GGTGGCTCACACCTG | 51366 |
rs551599301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102379450 | CAATAAATAATATTG[C/T]CATAATATTGTCATA | 51366 |
rs551621508 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102252194 | CTGAAAACACTCAGT[A/G]AAGTTCATTCTTGGT | 51366 |
rs551650149 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102323698 | TAGGCCAGGCGTGGT[A/G]GCTCACGCCTGTTAT | 51366 |
rs551690101 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102378079 | TCTCTAATCTAGAAA[A/C]CCTTCCTTCAACTAT | 51366 |
rs551702632 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102255122 | TGTGCAACACAGTGT[A/T]AATGATGCTCAGTAA | 51366 |
rs551790452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102324323 | GAAGGTTCCATGAAT[A/G]ATTTTTCTTTTAAAT | 51366 |
rs551790865 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102288893 | TATCTTGGCTGGGCG[C/T]GGTGGCTCACACCTG | 51366 |
rs551799665 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102333972 | TAATCCTGGAAGTTT[C/G]CAGATGTCAATAAAA | 51366 |
rs551799863 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102282499 | ATGGCGAAACCCCGT[A/C]TCTACTAAAAATACA | 51366 |
rs551821908 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102391702 | GTTTTCTTATAAAAG[G/T]GAGGGGGGAAATATG | 51366 |
rs551833854 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102305978 | CTCAAGTGATGCCCC[C/G]ACCTCAGCCTCCCAA | 51366 |
rs551838126 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102339757 | TTGATTGCCCCCACT[A/C]CTAAAAAAGCTACTC | 51366 |
rs551892168 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102255472 | AATCTGAAAAGAAAT[A/G]GAAAACAGGTACTCT | 51366 |
rs551913486 | snp | A/G/T | 0.0942338 | 0.195895 | intron-variant | UBR5 | GRCh38.p7 | 8:102281009 | AGACTCTGTCTCTTT[A/G/T]AAAAAAAAAAAAAAA | 51366 |
rs551955093 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102326447 | GTTACTGGAAACCGA[C/T]TCTTCAAATGATGCT | 51366 |
rs552038047 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102327059 | CACCCACCACCACAC[A/C]CAGTTACTTCTTGTA | 51366 |
rs552043598 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102317534 | CAAACAAAAAGACAG[C/G]AGTAACCTCTGCAGA | 51366 |
rs552054481 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102305440 | GTGGCCTACCAAAAG[A/G]AACAGAACTTAAGGG | 51366 |
rs552074326 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102325338 | CATGAAGAAAAAGAA[G/T]AGGTACATTTTACTT | 51366 |
rs552074950 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102392685 | CTAAAGATCAGAATA[C/T]AGTGACAAGAACTAG | 51366 |
rs552091371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102311610 | AATAAGAAACCTAGT[A/G]TTCAAATGTGCTAAA | 51366 |
rs552107793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102362135 | AAACCAGATCATCAA[C/T]GTCCTTATCTATATA | 51366 |
rs552120864 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102302868 | GGCAGCCCTGAGTTT[C/G]AACTGGTTAAGAGCA | 51366 |
rs552132732 | in-del | -/TATC | 0.00199481 | 0.0315187 | utr-variant-3-prime, downstream-variant-500B | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102252550 | GATGTATAAATTTTA[-/TATC]TATCTTTCAAACACA | 51366 |
rs552136745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102403489 | AGGTCAAGGCTGCAG[C/T]GAGCCATGTTCACAT | 51366 |
rs552198151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102402588 | GGCTTAAAAAACCAT[C/T]TTCCTCCACTTCTCA | 51366 |
rs552200505 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102410689 | CTAAACCGCCAGCTC[C/T]GGATTTAAAAGCTGT | 51366 |
rs552214127 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102347155 | GATTGCTTGGTTTTC[A/G]TTATTATTATTTTCA | 51366 |
rs552214631 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102409895 | CCTATCTTAAATGCT[A/G]CCTTCACAAATCTCA | 51366 |
rs552240291 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102366099 | TTCTCAAAGACAGAA[A/T]GGTATTTCTGACATC | 51366 |
rs552244942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102360331 | GGTACCTACTAAACA[C/T]GTAATATCATTCTTC | 51366 |
rs552257150 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102310331 | CTTTTTCCCTTTTTT[A/T]AAAATGTTTTTTGTT | 51366 |
rs552264424 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102280233 | AATGTATAACGCAAG[A/C]ATGTGTAAGCAAAAA | 51366 |
rs552275355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102265587 | ATACAGAATTCTGTC[A/G]TCACTTTGATGAGTT | 51366 |
rs552307100 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102312710 | CCCACACAGCCAGTG[A/G]TTACAGTCAGTGAAT | 51366 |
rs552317720 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102312011 | GATACATGCCATTCC[A/C]TAATGTTACAGATAG | 51366 |
rs552320534 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102257436 | AGCTAAATGTACTTC[A/C]CTCTGCTTAGAGCTT | 51366 |
rs552331891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102383919 | CAAGCAGAAAGAATC[A/G]AAACAGCACTGAACT | 51366 |
rs552382727 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102398248 | CTCTTCAATAAATGG[G/T]GCTCAGAGAATCGGA | 51366 |
rs552387031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102405964 | AATTAAATTTTCCTT[C/T]GGAAACTATTTCCTA | 51366 |
rs552396401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102294823 | TTTCCAGAGAAAGGA[A/G]CGATGCAATGCCACC | 51366 |
rs552410083 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102351594 | AAAAGTTCTAGAAAG[C/T]TGTTTCACAACAACA | 51366 |
rs552421868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102260039 | CTTAAAAAAAAAAAT[A/G]TTTTTTTTTACCCTG | 51366 |
rs552436048 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102310969 | TGCTCTTGGTGCCTG[G/T]GATAATACCTCCCAA | 51366 |
rs552449385 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102405518 | AGAGTCTGTTTTCTT[A/T]ATTAGAAATATGTAT | 51366 |
rs552478540 | snp | C/T | 4.03983e-05 | 0.00449417 | intron-variant | UBR5 | GRCh38.p7 | 8:102361576 | TAAATATTTTAAAAC[C/T]CTTACCTGTTTAAAT | 51366 |
rs552484364 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102410684 | AGAAACTAAACCGCC[A/G]GCTCTGGATTTAAAA | 51366 |
rs552485722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102361279 | GTTTACTCTTAAATA[C/T]AATTAGAAAAAAAAA | 51366 |
rs552505175 | snp | G/T | 1.64836e-05 | 0.0028708 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102277141 | TTTGCCGGTTTTGCA[G/T]GTTCATTACATTTTT | 51366 |
rs552543004 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102307385 | CCTCTGTATCATCAC[C/T]TCCTTTAGTTTGAAA | 51366 |
rs552545340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102309760 | ATGTTTGTACAACAA[C/T]GAAATCACCTAACAA | 51366 |
rs552563098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102352984 | CCAGTTTCTCCATTC[A/G]CCTGACTGTTACCAT | 51366 |
rs552614000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102265000 | ACAGGTGTGAGCCAC[C/T]GCACCCAGCGTACAT | 51366 |
rs552625002 | in-del | -/ACAAACAA | 0.00358779 | 0.0422022 | intron-variant | UBR5 | GRCh38.p7 | 8:102324090 | CCCATCCATTCTGCT[-/ACAAACAA]ACAAACAAACAAACA | 51366 |
rs552632280 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102316371 | AGAAAATACATTGAT[G/T]TGTTAAATGTTCTTT | 51366 |
rs552647534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102284939 | CTACTCGGGAGGCTG[A/G]GGCAGGAGAATGGCA | 51366 |
rs552668013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102335737 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCACTT | 51366 |
rs552686392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102372682 | ATTTCTATTAAACTC[A/G]GAAAATTCATGTTTC | 51366 |
rs552712051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102337947 | ACCTAATTAAAAGAT[C/T]ACCTCTTCTCACCAA | 51366 |
rs552725623 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102322520 | GTTCAACCATTGTGG[A/G]AGTCAGTGTGGCGAT | 51366 |
rs552744975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102390462 | AGCCTCGGCAACAGC[A/G]AGACTCTGTCTCAAA | 51366 |
rs552763607 | snp | A/T | | | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102413663 | TCTTTTTTAGTAGAG[A/T]TGTGGTTTCACCATG | 51366 |
rs552777487 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBR5 | GRCh38.p7 | 8:102355257 | CCCAGCAGCAAAAGT[A/G]AGCAGGCCTAGACTC | 51366 |
rs552778697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102346704 | AGGTTGCAGTGAGCT[A/G]AGATCATGCCACTGT | 51366 |
rs552781205 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102408736 | AGGGGAAAACGGAAT[C/G]AAAACACTAAGACAG | 51366 |
rs552799218 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102383216 | GAAGCCTGAGGGTAA[C/G/T]GCAAAACAGGAACTG | 51366 |
rs552819718 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102255408 | TCATCTAGAATTCTA[C/T]ATAAAGGGACAGAAA | 51366 |
rs552820958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102346142 | TCTACCACCTTGAAA[A/G]GAATATTCAGAAAAG | 51366 |
rs552861146 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102270734 | ATGTTGGTCAGGCTG[G/T]TCTTGAACTCCTGAA | 51366 |
rs552863655 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102277692 | GCCTTACCCACCCCC[A/C]TCCTTTAAATTCACT | 51366 |
rs552888824 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102373740 | GGTTATATTCCTGAT[C/T]GAGGATCTTGATGCC | 51366 |
rs552900071 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102293468 | AAAATATTTAAAATT[C/T]CGGCTTTCTGGTTGT | 51366 |
rs552945283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102356241 | GATCACTTGAGGTCA[A/G]GAGTTCAAGGCCAGC | 51366 |
rs552948666 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102353653 | CACCACTCATTAATT[C/G]TAACACATGTACCAT | 51366 |
rs552971065 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102263074 | CACGGGCAATGGAGC[A/G]GGACTCCATCTCAAA | 51366 |
rs552977028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102328170 | TACCAATTTTTAAAA[A/G]AATTTAGTGACTTTA | 51366 |
rs552986222 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102367752 | GGCTGGGAATGACAA[A/C]GAGCCAGGAAGGATT | 51366 |
rs553012285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102291438 | CAGATTTCACATGAG[A/G]GTCTGGAGGCTAAGC | 51366 |
rs553020365 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | UBR5 | GRCh38.p7 | 8:102335262 | AGTGGTTACCATGGG[C/T]TGACAAGCAGTGTGG | 51366 |
rs553041419 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102329809 | ACTTGACATATTTAT[C/T]TGTTTATACACTATC | 51366 |
rs553047442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102327249 | TAGGAAACTCCCCTA[C/T]ATATTGTTTCCAAAA | 51366 |
rs553059809 | snp | A/C | 3.30376e-05 | 0.0040642 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102326614 | GCTTTTTATTTTTTG[A/C]TCTAGCTTTCTCTAA | 51366 |
rs553146136 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | UBR5 | GRCh38.p7 | 8:102318403 | AAAAAAGAATAAAAA[C/G]AAACGAACAAAGCCT | 51366 |
rs553147368 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102315133 | TTATCTAGAAATAAC[A/G]AAATTTACACTTAAT | 51366 |
rs553158775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102358543 | GAAATAAAATTTCAT[A/G]TTATTACATGCTATT | 51366 |
rs553170149 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102357461 | CCTAGCTACTTGGGA[A/G]GCTGAGGCAGGAGGA | 51366 |
rs553214990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102254785 | TTTCATCTGTAACAT[A/G]AGGCTGTTGGACTAA | 51366 |
rs553240857 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102345785 | ATAACACTTGTGGCC[A/G]GGCACGGTGGCTCAC | 51366 |
rs553252320 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | UBR5 | GRCh38.p7 | 8:102342025 | AAAGAACACAGATCC[C/T]TAATCTTGTCATGAT | 51366 |
rs553263944 | snp | C/T | | | intron-variant, downstream-variant-500B, nc-transcript-variant | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102252135 | TTTTACTGGATAGTC[C/T]TGGTATCCAGATGAT | 51366 |
rs553266089 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102370572 | CATTTATCATTTGTG[A/G]TAAGAACATTCCAGA | 51366 |
rs553268855 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102255508 | TGAAGTTGATCTAAA[C/G]CACTCATTTCATAGA | 51366 |
rs553286485 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UBR5 | GRCh38.p7 | 8:102356833 | GAAAGTTCTTCCTTA[C/T]AGTTGAATTCCAATT | 51366 |
rs553301843 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | UBR5 | GRCh38.p7 | 8:102320818 | AATCCAGCATATAAA[C/G]AGAACCAAAGACAAA | 51366 |
rs553314451 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102328817 | TGGGTTGGCTAGGCT[A/G]GTCTCGACACCTGAC | 51366 |
rs553325306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102364141 | AACTCTTTTAGTCAT[C/T]TCCGGTTCTGAAAAT | 51366 |
rs553328959 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102261572 | TGGGCGTGGTGGCGC[A/G]TACCTGTAATCCCAG | 51366 |
rs553330399 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102315571 | ATCATCTTAACCCTC[A/G]TCTCCTATTACTCTC | 51366 |
rs553334357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102393469 | GTGAAACCCCGTCTC[C/T]ACTAAAAATACAAAA | 51366 |
rs553339456 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102371587 | TCTGGGTTGTTTGTT[G/T]TTTTTTTTTTTGAGA | 51366 |
rs553348371 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102399905 | GAGCCGAGATGGCAC[C/T]GCTGCACTCCACCCT | 51366 |
rs553401772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102269370 | TTTTAGGTTTTTTTA[C/T]ATCTCTGAGTTAAAC | 51366 |
rs553440551 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102406580 | ATTACAGGCATGAGC[A/C]ACCGCACCTGGCATA | 51366 |
rs553440708 | snp | A/T | 0.0197687 | 0.0974348 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102414539 | CAGATCTAAAAAAAA[A/T]TTTTTTTTTTTGAGA | 51366 |
rs553442155 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102304922 | ACACACTGGTGCAAA[A/T]TTTTTTTTCTTACAT | 51366 |
rs553443813 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102391762 | TCCTGAATTGTAGAC[A/G]CTGGTTAAAGTAAGG | 51366 |
rs553451387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102348008 | AAGGCAGGTGGATCA[C/T]GAGGTCAGGAGTTCA | 51366 |
rs553471263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102378748 | ACAGACTCAACAAGC[A/G]GTTCCAGACTAATAT | 51366 |
rs553482758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102311132 | AACACTTAAATTACA[C/T]GATAATCACTGATGT | 51366 |
rs553483803 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102280835 | CATCATGAGACACTG[C/T]CTCTCCAAAACATTA | 51366 |
rs553490748 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102313107 | TTTTAAGCCCGTATC[C/T]AATTCTCAGAAGAAA | 51366 |
rs553503667 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102413964 | CTAAAAATGCAAAAA[C/T]TAGCCAGGCATGGCT | 51366 |
rs553516981 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UBR5 | GRCh38.p7 | 8:102394103 | GGACTCTCGCCCTCG[C/T]CCAGGCTGGAGTGCA | 51366 |
rs553523765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102325917 | CCTTCTTCTGACAAA[A/G]CTAATTCAGCTAATA | 51366 |
rs553610269 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102307779 | ACAGTTGGTCCCAAC[A/G]TCCTGCTTGACATGT | 51366 |
rs553630750 | in-del | -/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102414116 | CATCTCAAAAAAAAA[-/T]TTTTTTTAATCAAAT | 51366 |
rs553630993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102262227 | TATTTAAAGAGATAA[A/G]TTTAATAAATCTTTG | 51366 |
rs553634687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102297405 | TAGTGATAGTCATAG[C/T]GAAAAAAGACACAAA | 51366 |
rs553636618 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102333405 | GCATGTTTCCTTAAA[A/G]AGCAGTAGTTTGTAG | 51366 |
rs553640292 | in-del | -/CTGATT | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102315866 | TAATATTTGAAATGG[-/CTGATT]CTGATTTCAAGGAAG | 51366 |
rs553657869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102313306 | AGACATTCTACAACT[A/G]CAAGTGCATTTTAAA | 51366 |
rs553664274 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102407691 | CCCAGGAGGTGGACG[G/T]TGCATTGAGCCGAGA | 51366 |
rs553675509 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102328030 | TTAAATGCTATAAAA[A/G]TAAGTAATTCAGAGA | 51366 |
rs553696891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102306906 | AGCAAAAGGCAGAGT[A/G]AGTTCAATAAAAAAT | 51366 |
rs553725921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102407056 | CTTAAAATGTGACTA[A/G]CTACAGATGAAGTGA | 51366 |
rs553728868 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102384146 | GAACTTTCTAAACAA[C/T]CAAAATAGATCCAAA | 51366 |
rs553753842 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102347564 | GTGTGTACTACCATG[C/G]CCAATTCCAATTTTT | 51366 |
rs553806181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102390721 | ATTGCTTCCACATCT[C/T]TTGAAGCTAAGCCAC | 51366 |
rs553821853 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102355505 | GAAACACATTTACTA[C/T]AAAGGAAAATATGTG | 51366 |
rs553830322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102339987 | CAAAATAATGCAAGT[C/T]ACCAAGATTTTTTTT | 51366 |
rs553841613 | snp | A/T | 0 | 0 | intron-variant | UBR5 | GRCh38.p7 | 8:102267674 | TCAACAGTCTTTGGC[A/T]TGGACCATTAAAAGG | 51366 |
rs553852105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102404823 | GAGGCAGGAGAATCA[C/T]TTGAACCCGGGAGGC | 51366 |
rs553938885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102377650 | GGCAGAGGTCGCAGC[A/G]AGCAGAGATCGCGCC | 51366 |
rs553942131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102362370 | ATTTTACAATGTAAA[A/G]ATATAATCAAATGCA | 51366 |
rs553979856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102289913 | CTGTCCATTAACAGC[A/G]AGTGTTTAATAGAAG | 51366 |
rs553980135 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102274348 | GACTGCTACTGTGTA[A/T]GTTGTGGCATTAAAA | 51366 |
rs553980388 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102411989 | CCCCCGCGGCCCCCT[G/T]CCCCCGGGATGAGAA | 51366 |
rs553990747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102397119 | CTCAGATATCCTATC[C/T]TCCCTCCATCAATGC | 51366 |
rs553991159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102378229 | CTCTGTGTGGTATCA[C/T]AACTACCACAATAAA | 51366 |
rs554016884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102340877 | TTCTTCCATTCACTC[A/G]GTGGCTAAACAAACC | 51366 |
rs554017659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102346486 | GACAGGATGTGGTGG[C/T]TCAAGCCTGTAATCC | 51366 |
rs554051550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102398865 | ATGGGAGAAAATATT[C/T]ACAAACTATCCACCT | 51366 |
rs554078706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102385342 | TGTTCTGTATTTCAT[A/G]CTTACTGTAAAAATA | 51366 |
rs554080112 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102348692 | ATCATATGACCTAGA[A/G]AGAGGTATTTTACTC | 51366 |
rs554081254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102369331 | AGGTTGAGAGCAATG[C/T]GGAAATCTGAAACCT | 51366 |
rs554089497 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102317361 | ACTCTGAGATCAAAC[A/C]GCAAGGCGGCAGCCA | 51366 |
rs554096832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102288476 | CGAGACGGAGATGGG[C/T]GGATCACAAGGTCAA | 51366 |
rs554137670 | in-del | -/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102392623 | AAAAAAAAAAAAAAA[-/C]AAAAAACAAAAAACA | 51366 |
rs554141257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102367415 | TTCTGATGATCATTT[A/G]CTGGTGCCAACATCT | 51366 |
rs554142947 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102288921 | CTGTAATCCCAGCAC[G/T]TAGGGAGGTTGAGGC | 51366 |
rs554153120 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102268493 | ACAGGTGAGAGCCAC[C/T]GCACCCGGCCTTATC | 51366 |
rs554164935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102324818 | CAACAGTTCTTTTCA[A/G]TGTTAAGACATGAAT | 51366 |
rs554168809 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102321107 | ATTAGGCAGGAGAAG[G/T]AAATAAAGGGTATTC | 51366 |
rs554179182 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102331883 | TACCATGCACTCCCT[G/T]CCACTGATTCTGTGT | 51366 |
rs554180769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102338805 | TGACTTCAGAGTCCA[C/T]ACTCTTTGTAATCAT | 51366 |
rs554251585 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102329980 | TCAAATCAAAAGATT[A/C]TTTCCCTGTAAGCTC | 51366 |
rs554256391 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102324394 | GGGTTTAGGAGTAAA[C/T]AACTTACAGAGAAAA | 51366 |
rs554263407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102272919 | GAGTTCTCAGAAGCT[C/T]ATCCATTACAAAATA | 51366 |
rs554289436 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102338097 | GAAGGATGGAAAGAA[A/T]GGCTAGAGAAGGGTG | 51366 |
rs554299925 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102322689 | AGACTTGGAACCAAC[C/G]CAAATGTCCAACAAT | 51366 |
rs554329391 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102332231 | TTCTTCTCTTTCTCT[C/T]TCCCCATACCCCTGC | 51366 |
rs554330039 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102348338 | AAAAAGTAAAATTCA[C/G]AGTTTAGAATTCAAA | 51366 |
rs554339786 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102370215 | TCTGTGGCCCAAGCT[A/G]GAGTGCAATGGTGTG | 51366 |
rs554358798 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102394995 | ATTCTGGGCTTCTTT[C/T]AGTTCCTCAAATACA | 51366 |
rs554380811 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102266334 | TGTATCCTGGGCATT[C/G]TGAATTAGTTGTGAA | 51366 |
rs554399419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102317123 | CCAGCCGAAGCAGGG[C/T]GAGGCATTGCCTCAC | 51366 |
rs554401642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102361810 | CAGACTCTGCAATTC[C/T]GTTCCCTCACCACCC | 51366 |
rs554415525 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102368814 | AGAAAATGCATATAA[C/T]ATTATTTAACACAGT | 51366 |
rs554428916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102353878 | AGTCTCCACAAAAAA[A/G]TAATTAGCTGGGCAT | 51366 |
rs554456403 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102323766 | GTCAGGAGTTCAAGA[A/C]CAGCCTGGCCAAGAT | 51366 |
rs554495728 | snp | A/C | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102414081 | CACTGCACTCCAGCC[A/C]GGGCAACAGAACGAG | 51366 |
rs554512033 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102332660 | CTGCTTAAATGCTAT[C/G]TCCTCTGCGATGCCT | 51366 |
rs554525519 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102409353 | ATGCTTTGTACATTT[C/T]AGACACTTGAGACAT | 51366 |
rs554549583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102287341 | GCTTAGCTACCCTTG[C/T]GTATATCACACAAAG | 51366 |
rs554553814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102308693 | TTACTTTAGAATGTA[C/T]TTCTTCTATCTATTT | 51366 |
rs554576188 | snp | C/T | 0.000495802 | 0.0157371 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102265126 | TCTGAAACAATTCAA[C/T]CTTGCTTCTGTGTTC | 51366 |
rs554600274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102316552 | ATGAGTAGATGTTTC[C/T]AAAAGCACAGGTGTT | 51366 |
rs554620064 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102374518 | AACTAAATCATACTC[A/T]CAAACTACTCTTTTA | 51366 |
rs554637817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102307927 | ACTATTCTCAGGACT[C/T]AGTCCTTGGACCTTT | 51366 |
rs554644306 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102321832 | TGAGAAAAACAAGCA[A/G]TGGGGAAAGGATTCC | 51366 |
rs554649560 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102312280 | TTTTGCTTTCAAACT[C/T]CATAATAAACTCACG | 51366 |
rs554673471 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102253838 | ACAAGTTCCATATAC[A/G]TGATACACAGTTGCA | 51366 |
rs554676448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102314457 | GTCTCAACAAAAGTG[A/G]GTAGATAGACTAGCT | 51366 |
rs554689838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102350971 | TAATCATCAGAGAAA[C/T]CCAAACCAAACTACA | 51366 |
rs554711580 | snp | C/T | 8.26016e-05 | 0.00642604 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102329372 | GTTCAGAATACAGAG[C/T]CCCAATACAGATGAA | 51366 |
rs554720242 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102294418 | AAAACATAAACTCAG[A/T]CTGGGGCACTTTCCA | 51366 |
rs554734458 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102382853 | ACACACACACACACA[A/C]ACACACACAGAGACA | 51366 |
rs554736824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102263882 | AGGTGCATGCCACCA[C/T]ACGCAGTTAACTTTT | 51366 |
rs554757554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102400604 | AAACTCTACCTCTTG[C/T]AGCAGTCTTTCATAG | 51366 |
rs554766222 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBR5 | GRCh38.p7 | 8:102282156 | CCTGGGCAACAGAGC[A/G]AGACCCTGTCTCAAA | 51366 |
rs554773320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102353202 | ACAGTACTGGAATCA[A/G]TTGATTCCTTTTATC | 51366 |
rs554810925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102310450 | CTCCGGGGTTCAAGT[A/G]ATTCTTGTGCCTCAG | 51366 |
rs554838819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102402765 | CCTGGAATACCTCAT[C/T]GCCTGAATTCTGAAC | 51366 |
rs554859751 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102391425 | GATATTAGGGAATTT[C/T]TGTTAATTTCCTATA | 51366 |
rs554869022 | in-del | -/TT | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102264273 | CATCTCCCCATAGTC[-/TT]TTTCTGTCATTAATT | 51366 |
rs554892597 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102294294 | CCTGCCAATGTGCTT[C/G]ACATACAGTGAGTCC | 51366 |
rs554899699 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102283657 | CAGGAAAGCTGCTAC[C/G]TCTCAAATCACTATC | 51366 |
rs554908711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102293021 | AGGTCCTTATTAAAA[C/T]ATCATCACACATGCA | 51366 |
rs554909884 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102351606 | AAGCTGTTTCACAAC[A/C]ACAGTGTGGACATAC | 51366 |
rs554919160 | snp | A/C | 1.74769e-05 | 0.00295603 | intron-variant | UBR5 | GRCh38.p7 | 8:102300196 | ACTACCATATCTACA[A/C]ATAATGAAACGGTGT | 51366 |
rs554932752 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102309559 | TGTGCTAAATGCCCT[A/G]TCAGGTGCACCTTTT | 51366 |
rs554983177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102256195 | GTAGTCCCAGCCACT[C/T]GGGAGGCTGAGGCAG | 51366 |
rs554984115 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102386647 | AGCACAGTCCTTTAC[G/T]ATGACATTCTGTTTT | 51366 |
rs555035455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102408450 | CCTTTTGATATGACA[A/G]TCTCAATAAAGACTG | 51366 |
rs555041073 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | UBR5 | GRCh38.p7 | 8:102379049 | TGCTTTTTTTTTTTT[A/T]TAAAAATGCCTGGAA | 51366 |
rs555137197 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102380167 | GGGAGGCCAAGGCAG[G/T]CACATCACTTGAGGT | 51366 |
rs555138386 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | UBR5 | GRCh38.p7 | 8:102365379 | CTGAGGCAGGAGAAT[A/C]GCTTGAACCCGGGAG | 51366 |
rs555138457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102357635 | CCTGGACTGAATCCT[A/G]GACAAAAGGGTATTA | 51366 |
rs555163107 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | UBR5 | GRCh38.p7 | 8:102277837 | CTGTCTCTACTAAAA[C/G]TACAAAATAATTACC | 51366 |
rs555163146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102285857 | GATTATATATACTTA[C/T]GTAAATCTAAATGGT | 51366 |
rs555226103 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102292502 | GTTTAGAGATGAGAC[C/G]ATCCCAAAATCTGTT | 51366 |
rs555231296 | in-del | -/A | 0.0722614 | 0.17581 | intron-variant | UBR5 | GRCh38.p7 | 8:102339530 | GCGAAACTCCATCAC[-/A]AAAAAAAAAAAAAGG | 51366 |
rs555232071 | in-del | -/AGG | 0.00438332 | 0.0466095 | intron-variant | UBR5 | GRCh38.p7 | 8:102372440 | GAATCATAGTTTGTA[-/AGG]AGGACTTACACTTTT | 51366 |
rs555251029 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102285032 | AGAGTGTGAGACTCC[A/G]TCTCAAAAAAACAAA | 51366 |
rs555257145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102395599 | AGGCTAAGTTAATGT[A/G]GGGTGGAGTCTTTGC | 51366 |
rs555261886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102284451 | AGTATCAGATTCCTA[C/T]GATATGAATGGATTT | 51366 |
rs555268285 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102349011 | TGCTGATGCACACTA[C/T]CAATTCATGTTTATG | 51366 |
rs555271140 | in-del | -/AACT | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102300939 | AATTAATACATTTAG[-/AACT]AACAATGATTTAAGA | 51366 |
rs555289437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102344007 | CATAACACTATTACA[C/T]AGTGCATTCAATATA | 51366 |
rs555306820 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102269770 | AAATATAATGCACAG[A/C]AAATTCTTTAGCATG | 51366 |
rs555367888 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102319036 | ACTGCATCAACTAAC[A/G]AGCAAAATAACCAGC | 51366 |
rs555369413 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102334639 | GCCGTGGCTCACGCC[C/T]GTAATTCCAGCACTT | 51366 |
rs555394774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102276427 | AAGCCAACATTCTGC[C/T]TCAGCATCTTTCCCC | 51366 |
rs555452933 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102399816 | CTGGGCGTGGTGGCA[C/G]GCGCCTGTAGTCCCA | 51366 |
rs555463411 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102323595 | ATATGAAAGTACTGG[C/G]CTTCCTAGGTTTCCC | 51366 |
rs555509166 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102274938 | AATATGCAACCTTAG[A/G]GCACAGACTGTAATC | 51366 |
rs555520861 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102253622 | GATACAAAGAAAAAG[C/T]TGATTGTGATAAAAG | 51366 |
rs555534015 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102270588 | GCAATGGCATAATCT[C/T]GGCTCACTGCAACCT | 51366 |
rs555547095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102341123 | CTAGATTAATAATAC[A/G]TGGTGGCCCTATTAA | 51366 |
rs555552176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102377577 | CGGGCATTGTTGGAC[A/G]CGCCTATAGTCCCAG | 51366 |
rs555566922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102319636 | ATCAACAGAATATAC[A/G]TTTTTTTCAGCACCA | 51366 |
rs555570614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102325901 | ATTCAATCTGTTGAT[A/G]CCTTCTTCTGACAAA | 51366 |
rs555578714 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102391810 | GTGTTCCCAGACAGT[C/T]AGGCATTCTAAGTCA | 51366 |
rs555582774 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102333312 | TAGAAAACAATGTTT[G/T]TATTGTTTTTATGAA | 51366 |
rs555625010 | in-del | -/AAT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102320796 | CAATATACGCAAATC[-/AAT]AAATGTAATCCAGCA | 51366 |
rs555646368 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102410353 | CTCTTCTCTCTGGTG[A/C]GGTTTTCTAAGTAAC | 51366 |
rs555650181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102297723 | AGAAATTATATATCA[A/G]TTTTAAAAAGTGATA | 51366 |
rs555673476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102371629 | AGTCTCGCTCTGTCG[C/T]CCAGGCTGGAGTGCA | 51366 |
rs555676309 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102363159 | CCCAGCCTGAAGTAA[C/G]TTTCAAATGCGGCCA | 51366 |
rs555690278 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102306364 | CTTGCCACCTTCTGG[A/G]AAACTGTCAAAATAA | 51366 |
rs555694111 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBR5 | GRCh38.p7 | 8:102362184 | CCATTTCTAACAGCA[C/T]TTAAAACAGTACTGA | 51366 |
rs555703727 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102335008 | GAAAAAGCTTAAGTG[C/T]CCTTCATGGACAAAT | 51366 |
rs555706729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102356176 | AAAATAAGGCCAGGC[A/G]CGGTGGCTGACACCT | 51366 |
rs555762932 | in-del | -/AAAC | 0.00557542 | 0.0525036 | intron-variant | UBR5 | GRCh38.p7 | 8:102282171 | AGACCCTGTCTCAAA[-/AAAC]AAACAAACAAACAAA | 51366 |
rs555818343 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102317675 | CCCCAAGCAGCCTAA[A/C]TGGGAGGCACCCCCC | 51366 |
rs555837335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102354713 | AAAGAAAGAAAACAG[C/T]AGCAGCTAGAAATCT | 51366 |
rs555838244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102310544 | TAGAGATAGGGTTTC[A/G]CCATGTTGGCCAGGC | 51366 |
rs555874943 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102317098 | GACAGTGGGTGCAAC[A/G]CACCGTGCACCAGCC | 51366 |
rs555880815 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | UBR5 | GRCh38.p7 | 8:102356708 | GAGCTTGCAGTGAGC[C/T]GAGATCGCGCCACTG | 51366 |
rs555904307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102395221 | ACTGGTGCTTCTAGT[A/G]AAGAATCCTGAACTT | 51366 |
rs555905633 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102308151 | CCAAATTCCTGAACC[C/T]TCACCTTCACTTCTT | 51366 |
rs555907825 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102339915 | CTATTGTGTACAAAA[G/T]TGAGACTATCCTTTA | 51366 |
rs555912554 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102404706 | TGAGGTCGGGAGTTC[A/G]AGACCAGCCTGACCA | 51366 |
rs555952288 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102406925 | AATGCCAAGACTTGT[A/C/G]CAAAAACACACTTTC | 51366 |
rs555980026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102411800 | GTCTCAATTCAACTT[C/T]GACTAATATGGATTC | 51366 |
rs555987542 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102281940 | TTCATTAAAATGACA[C/T]CAAAAGCACAAGCAA | 51366 |
rs556019910 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102347944 | TAAAATGAACACATT[A/G]GTCAGGCATGGTGGC | 51366 |
rs556038152 | in-del | -/A | 0.189261 | 0.242509 | intron-variant | UBR5 | GRCh38.p7 | 8:102396710 | CACATATATATATAT[-/A]TTTTTTTTTTTCTTG | 51366 |
rs556060187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102385283 | TCAAAATAGATCTCA[C/T]AACTAACTCAATACC | 51366 |
rs556080656 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBR5 | GRCh38.p7 | 8:102347502 | TAGTCTCAAAACTCC[C/T]GGGCTCAATCTTCCT | 51366 |
rs556091908 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102312658 | GAGCTTTGCTACTGA[C/G]ATCTATATTCAAGGC | 51366 |
rs556129061 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBR5 | GRCh38.p7 | 8:102318276 | AAAGCCAAGGCTCGA[A/G]AACTACGTGAAGAAT | 51366 |
rs556134794 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102304223 | AGAACTAATACACTG[A/T]GTATGTATAGTCCAC | 51366 |
rs556165122 | in-del | -/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102332145 | ATCGAATTGACTGAT[-/G]GAGAGAAAAGGAAGA | 51366 |
rs556170456 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102296166 | CCTGGCATCTAGTAC[A/C]CTTGGAAAACAATCA | 51366 |
rs556191380 | snp | C/T | 0.0836354 | 0.186609 | intron-variant | UBR5 | GRCh38.p7 | 8:102396641 | ATATATATACACACA[C/T]ATATATATACACACA | 51366 |
rs556222349 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102275361 | ACACACACACACACA[C/T]GAAAAAATAAATTTG | 51366 |
rs556224219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102293334 | CTTACAGTGTAATTA[A/G]GGAAACTATCAAACA | 51366 |
rs556226989 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102259738 | ACAGGGATCAGAAAC[A/C]CTCAACACCATCAGT | 51366 |
rs556230359 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102411359 | ACTATCATTAGAATA[G/T]AAAAGGAAACAAAAA | 51366 |
rs556251422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102360819 | ACCTGAGATGGGGAA[A/G]TATGACATACATAAC | 51366 |
rs556254517 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102395834 | CATGTGGCAGTACTA[A/G]GACCTAATAAACAGC | 51366 |
rs556284338 | in-del | -/T | 0.0019972 | 0.0315375 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102411280 | TGCGAACTGCAAACG[-/T]TAAGAGTTTTCCTTT | 51366 |
rs556292361 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102332847 | TCATACTCATGACTA[A/T]ATTACCATATGCCAG | 51366 |
rs556312363 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102386907 | CTTGAACCCAGGAGG[C/T]GAAGTTTGCAGTGAG | 51366 |
rs556320522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102369213 | AAAGCTGGCCCTAGA[C/T]AGAAAAGTTACGGAA | 51366 |
rs556329858 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102270890 | TTCAAATAGGAACTT[A/G]AGTCAGATAAAAAGA | 51366 |
rs556330911 | in-del | -/AAT | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102314432 | ACATAATCAATTTAC[-/AAT]AATAAGAGTCTCAAC | 51366 |
rs556362053 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102384451 | TTACGCCTGTAATCC[A/C]AGCACTCAGGGAGGC | 51366 |
rs556366722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303029 | ATGGCAGCACTGGCA[C/T]TGGACCAACCATATC | 51366 |
rs556367819 | in-del | -/CTCACTGGCCAGGCACAG | | | intron-variant | UBR5 | GRCh38.p7 | 8:102365177 | ACATTAGAATATAAC[-/CTCACTGGCCAGGCACAG]TGGCTCATGCCTGTA | 51366 |
rs556372240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102296774 | CTTAAACAAGGGAAA[C/T]GTAAGTAACCTCATG | 51366 |
rs556449015 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102391213 | TGCTTTAACATAGAA[A/T]GTCAACATCAAATGA | 51366 |
rs556496788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102382291 | CAACAGAATCACCTG[C/T]GGAGGGGGCGTCTCT | 51366 |
rs556512805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102280308 | ATTCCCACCCAGACA[A/G]AAAATAATGAAGTTA | 51366 |
rs556527822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102365426 | AGTGAGCCGAGATCG[C/T]GCCACCGTGCTCCAG | 51366 |
rs556540279 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102373534 | TCTCCCAAATGCAGA[A/T]AATGTATTCAAATTA | 51366 |
rs556557298 | in-del | -/AA | 0.409382 | 0.192607 | intron-variant | UBR5 | GRCh38.p7 | 8:102300483 | GCTAAACATTAAAAC[-/AA]AAAAAGTTTCTATCC | 51366 |
rs556559990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102390005 | ACCTCATGATCTGCC[C/T]GCCTCGGCCTCCCAA | 51366 |
rs556636994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102278646 | TATGGATGAAGTGAT[C/T]TGACAGCAAGTTAAT | 51366 |
rs556642530 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303558 | TTCATATTCATTATC[C/T]AGTCAAATACCTAGC | 51366 |
rs556694139 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102381181 | GACCAGCCTGGTCAA[A/C]ATGGTGAAACCCCGT | 51366 |
rs556710393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102329884 | AACTTAGCGTACAAG[C/T]AGGTGCTCAATCAAT | 51366 |
rs556733502 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102257330 | TAAGGATGTATACAG[A/G]GAGAAGCATATGTAG | 51366 |
rs556750093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102273459 | GAGCAATCAGGCATT[C/T]TCACATTGATGGTGA | 51366 |
rs556757513 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102312715 | ACAGCCAGTGATTAC[A/G]GTCAGTGAATGTTTT | 51366 |
rs556787739 | in-del | -/TTTTTTTG | 0.00358779 | 0.0422022 | intron-variant | UBR5 | GRCh38.p7 | 8:102406716 | GGGTTTTTTTATTGA[-/TTTTTTTG]TTTTTTTGTTTTTTG | 51366 |
rs556826503 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102384930 | AAGGGTTACTGAGTC[C/T]CTCAACACATACCAA | 51366 |
rs556836344 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102279821 | CCAACTGTCTTTCCA[C/T]AGGCTGAATAAAAGT | 51366 |
rs556853309 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102309847 | TCTAGTCACATTTCA[C/G]TCCTAACTCCACCCC | 51366 |
rs556862309 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102366283 | CACCCAGTTCAAATG[C/G]CACCTCCTCCATGAA | 51366 |
rs556869554 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102375212 | CTAAAAATACAAAAA[C/T]TAGTCAGGGGTGGTG | 51366 |
rs556872753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102271571 | ACGCTGAAATTTCTT[A/G]CATGACTAGACTCAT | 51366 |
rs556898425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102297806 | AAGCATAATTACATC[A/G]TACCCACATATGATG | 51366 |
rs556901813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102338064 | GCACAGATGGTTAGA[C/T]GGAAAGGTGGATGGA | 51366 |
rs556906605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102409970 | CTTTATAATTTCACC[C/T]ACGGCACCTTTCTAT | 51366 |
rs556948122 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102314355 | GAAAAAATTCTATCC[A/T]TGGTGTGGCAGTAAG | 51366 |
rs556961415 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102288328 | AATGCGAAGACCACT[A/G]ACTATAGAGAATTTG | 51366 |
rs556986689 | snp | A/C | 0.0279526 | 0.114869 | intron-variant | UBR5 | GRCh38.p7 | 8:102319468 | TACAAAGAGACTTAG[A/C]CTCCCACACACAATA | 51366 |
rs556992635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102272240 | TGCTGCAATTTGATC[A/G]GTGAATTTTTATATC | 51366 |
rs556993807 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102380394 | ACTCAAAAAAAAAAA[A/C]AAAACAAAAACAAAA | 51366 |
rs556997645 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102289734 | CAATACTTAATCTAT[A/G]TATCAGAAAATATAA | 51366 |
rs557008585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102328876 | AAGTGCTCGGATTAC[A/G]GGCGTGAGCCACCAG | 51366 |
rs557048395 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | UBR5 | GRCh38.p7 | 8:102318973 | ACAACCGGTACCAGC[C/T]GCTGCAAAATCATGC | 51366 |
rs557069656 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102414666 | AGCCTCCCGAGTAGC[C/T]GGGATTACAGGCGCT | 51366 |
rs557071302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102284986 | AGCTTGCAGTGAGCC[A/G]AGACGGCACCACTGC | 51366 |
rs557076449 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102323676 | CTTCATTAAGAAAAT[G/T]TGTTTCTAGGCCAGG | 51366 |
rs557089085 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102367136 | TTTCTAAAAAGACAA[C/T]CTATCTCTAACCACA | 51366 |
rs557090771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102301341 | TATGATGTATTTTTT[A/G]GAATAAAAACACTCT | 51366 |
rs557091971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102356947 | GAATCATCAATAAAT[A/G]CTAAACTCAGTGAGC | 51366 |
rs557095347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102343891 | GGGGGGAGAACATGG[A/G]AAGAGACCTTTAAAG | 51366 |
rs557105577 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102285457 | AATACTGGAATTCTC[-/A]TAATTGACAGCCAAA | 51366 |
rs557131568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102309385 | TAAGCATATTATTAT[C/T]ACAAACAAATCAAAA | 51366 |
rs557133308 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102359440 | TCACTTGAGGCCAGG[A/C]GTTCAAGACCAGCCT | 51366 |
rs557143589 | snp | A/G/T | 4.98081e-05 | 0.00499019 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102254335 | CTTGGTCTTAATGGC[A/G/T]AGTAACAATTTCTGT | 51366 |
rs557178095 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102414580 | GCTCTGTCGCCCAGG[C/T]TGGAGTGCAATGGCA | 51366 |
rs557195481 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102311932 | AATTGTTATACATCT[C/T]ATCTCTAATAAACAT | 51366 |
rs557202288 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102364208 | CTCTTTTGAGACTGG[A/G]TCTCACTCTGTCGCC | 51366 |
rs557207630 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102343115 | TATATAAGCAAACTC[A/G]AAAAATGCACACATA | 51366 |
rs557211929 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102351551 | TCTTGTTATTTAACG[A/G]GTATAAAGTTCCAAC | 51366 |
rs557213257 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102409245 | TTCCACCCCAGCCAT[C/T]CCCACCTGTATTTGT | 51366 |
rs557250427 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102364584 | ATATTCAATTTTTAT[C/T]GTACCCATTTGAAAC | 51366 |
rs557266841 | in-del | -/AGAAAAAAAGAAATGTGATTTG | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102284248 | CAGACTAGGGGAGGC[-/AGAAAAAAAGAAATGTGATTTG]AGAAAAAAAGAGCAG | 51366 |
rs557274155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102299655 | GCCAAAGGTCAAATT[A/G]GATAGAGTTTAAGTG | 51366 |
rs557274419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102357518 | TATAGTGAGTTATCA[C/T]TGTGCCACTGCCCTC | 51366 |
rs557282130 | in-del | -/AATT | 0.00557765 | 0.0525139 | intron-variant | UBR5 | GRCh38.p7 | 8:102263099 | CTCAAAAAAAAAAAA[-/AATT]AATTAATTAAAGCCG | 51366 |
rs557283585 | in-del | -/AAACTAT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102262794 | ATGTACCTCCGGAAA[-/AAACTAT]AACATAAATCCTCAA | 51366 |
rs557297110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102307811 | CTCTTCATTTGACTT[C/T]CAGGACACAACTCAT | 51366 |
rs557297706 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102289939 | AGAAGTGATCTAACT[C/T]TTAAGAGATCTGACA | 51366 |
rs557308063 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102321785 | TCAGAAATAATGCCA[C/G]ATATCTACAACTATC | 51366 |
rs557321345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102387348 | TATAAAACTCACAGT[C/T]CATTAGGTTTTTAAA | 51366 |
rs557328642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102315375 | GATTAAAAAACTAGC[C/T]CTCTTTAATGAGTTA | 51366 |
rs557339434 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102364658 | TATCAAATTTTAAAA[A/C]ACTCTTAAATTCAGT | 51366 |
rs557391569 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102398975 | AGCAAAAGGTCTGAA[C/T]AGACATTTCCCAAAA | 51366 |
rs557413561 | snp | A/G | | | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102254456 | ATTGTGATTGAGGGC[A/G]TAGGCTGGAATCCTT | 51366 |
rs557420742 | snp | C/T | 3.45179e-05 | 0.00415424 | intron-variant | UBR5 | GRCh38.p7 | 8:102296883 | TAAAGAAAACTAGAA[C/T]TGTACTCACTTGCAA | 51366 |
rs557431626 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102341004 | ATATTTTTAGCCAGG[A/C]CAACAACGGCTAGCT | 51366 |
rs557451492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102406272 | CAATAAATCTAGTAT[C/T]GGTTTTTTATTGTTT | 51366 |
rs557508020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102269706 | CAGCTTGCTAACAGA[C/T]AAAGTCTGCTCCAAA | 51366 |
rs557515240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102392693 | CAGAATATAGTGACA[A/G]GAACTAGTTTTTATA | 51366 |
rs557518180 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102372251 | ATTTCTAAATCAGTG[A/G]TCTCACTTTTCTCAC | 51366 |
rs557554520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102292447 | AAGAACAAGATGACA[C/T]AAAATCTTGAAACTT | 51366 |
rs557569780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102400943 | CAAGTTTGGCCCTAT[C/T]TGCCATCATCAATCA | 51366 |
rs557594658 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102305787 | ACAGTGTCTCACTCT[C/G]TCTTCCAGGCTGTAG | 51366 |
rs557633708 | in-del | -/GATATGACAATCTCAATA | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102408440 | GAGAAAAATCCTTTT[-/GATATGACAATCTCAATA]GATATGACAATCTCA | 51366 |
rs557646765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102401033 | GCTGCTCCTGATGAC[A/G]GTCCATCCCATGAGA | 51366 |
rs557648577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102394218 | TTCGCACACCACCAC[A/G]CCCAGCTAATTTTTG | 51366 |
rs557681827 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102353489 | TCATCAAAAACAAGG[-/A]AAAGTCTGAGAAACG | 51366 |
rs557701903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102400410 | AAAAGTTCCAAACAC[A/G]TCTCAACCCGAAGTT | 51366 |
rs557708891 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102276076 | GCTATGTCTTATCTT[C/T]GTCTTTCATTTTACC | 51366 |
rs557721899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102393238 | GAATCTTCATTTATA[C/T]TTAAGTTATGATGAA | 51366 |
rs557733070 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102376648 | AGCTAGGATTACAGG[C/T]GCCCGCTACCACACC | 51366 |
rs557746385 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102282841 | CTGGGATGGTTATAA[C/G]AAAAGACAGATAATA | 51366 |
rs557788738 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102308028 | CAGCTTGAGCCTTTC[A/T]CTCTTAGTCAGACTT | 51366 |
rs557802535 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102384312 | AGAATATTAAAGGTA[A/T]TATTTGTGTTTAAAA | 51366 |
rs557806999 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102253391 | AGTAAATGTAACAAG[A/G]TACTTAAAAAAGGCT | 51366 |
rs557822068 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102345630 | AAAAATTCACATACA[A/T]TTAAAAACTAGGGAA | 51366 |
rs557824116 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102411877 | AGAAACCACCCCCCC[A/T]TCTCCGCCGAGTTCA | 51366 |
rs557825239 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102306308 | GGTGGGAAAAGAGCA[C/T]GTGGGAGTATAAAGG | 51366 |
rs557845732 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102261513 | CGAGACCATCCTGGC[C/T]AACATGGTGAAACCC | 51366 |
rs557876791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102356065 | AATTTGAGCAACATA[A/G]TAAGAGAAATGGGTT | 51366 |
rs557909092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102281575 | AATGTGAAATTCACT[A/G]TCATAAATATGCAAA | 51366 |
rs557956967 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102327390 | AAAAAAATACTCTAT[A/C]ACCTATACTTTCAAT | 51366 |
rs557959711 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102332747 | TTACTCATACTTTCA[G/T]CCTAGCACTGATCAC | 51366 |
rs557970834 | snp | C/T | 1.65375e-05 | 0.0028755 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102327755 | ACCACCAATATAAAC[C/T]GTTTTCCAGCTGAGC | 51366 |
rs557973579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102371621 | AGTCACGGAGTCTCG[C/T]TCTGTCGCCCAGGCT | 51366 |
rs557975367 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102283464 | CTATGGAATTGGACA[C/T]TTTAAATGGGTGAAT | 51366 |
rs557994095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102378892 | ACAGGGGGGTTAGGG[A/G]TAGCGGTGGGGGACA | 51366 |
rs558003930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102386536 | ATACATGATAGTGAA[C/T]CTGTCCTCTGCCAAC | 51366 |
rs558044313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102274824 | AATTGGGAGTATCAA[C/T]ATTAATTCATTATTT | 51366 |
rs558085777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102362466 | TTTTCCAGAAATAAT[C/T]CTTGTAAAAGTAAAC | 51366 |
rs558106564 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102333210 | GCTTCAGATTTATCT[A/G]TATTAAAGAAATTTA | 51366 |
rs558149099 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102366854 | TAAATCACAGACTCC[C/T]GTAGAAAAAGTCTTC | 51366 |
rs558151698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102393236 | GGGAATCTTCATTTA[C/T]ATTTAAGTTATGATG | 51366 |
rs558163163 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102412672 | CCGCGCGTCACTAGC[A/G]AGAAGCTGCCGCCGC | 51366 |
rs558209126 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102324868 | TGTAACTGCCCTCAG[A/C]CTCCAGTATTCTACA | 51366 |
rs558228154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102323235 | ACCTCTAAGTCTTCC[C/T]TGATTATTCCCATTC | 51366 |
rs558236999 | in-del | -/AAAAAAC | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102302198 | CTCATATAGATTCTT[-/AAAAAAC]AAAAAACAAAAAACA | 51366 |
rs558283581 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102317054 | GTACCGGGTTCATCT[C/T]ACTAGGGAGTGCCAG | 51366 |
rs558284435 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102363047 | GTATAGATGGGGTTT[C/T]GCCATTTGGGCCAGG | 51366 |
rs558295691 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102347351 | AGTACACTACAGCCC[A/G]GAACTCCTGGGCTGA | 51366 |
rs558299973 | snp | C/G | | | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102279084 | GGCTTCAGCCAGAGG[C/G]ACTTCAAATGGATTT | 51366 |
rs558300977 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102373402 | ACCGAAAGACTTCTT[C/T]AGGGCTCCTGACCAA | 51366 |
rs558345560 | in-del | -/A | 0.0174175 | 0.0916809 | intron-variant | UBR5 | GRCh38.p7 | 8:102387430 | AAAAAGTTCCTGGTC[-/A]GGGGTGGTGGCTCAT | 51366 |
rs558364494 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102413776 | CCACCACGCCTGGCC[A/G]AGATAGGATCTTTTA | 51366 |
rs558445159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102317624 | GAGATCTGAGAACGG[A/G]CAGACTGCCTCCTCA | 51366 |
rs558522316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102258441 | TTTCAAAAGAAAGAA[C/T]TGCAGCAAATCAAAC | 51366 |
rs558526035 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102317378 | CAAGGCGGCAGCCAG[C/G]CTGGGGGAGGGGCGC | 51366 |
rs558534040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102301293 | AATTACTTTTAGAGG[C/T]TATGTTCAAGAGCAT | 51366 |
rs558536641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102310092 | AACATGTTTAAAACT[A/G]AATTCATCCTTTTCC | 51366 |
rs558556319 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102292394 | AGGGAATGGAATAAA[G/T]AGAGTTTAAGAGTAT | 51366 |
rs558565247 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102308288 | CTATAGTCTTCAACT[C/G]GGTAAATGACAACTT | 51366 |
rs558607126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102310492 | GCTGGGATTACAGGC[A/G]TGCGCCACCATGCCG | 51366 |
rs558613676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102265331 | CTGAAAAAACAAAAC[A/G]TATGAAATGGTTCTC | 51366 |
rs558614576 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102300296 | TACAAATGCCAATTC[G/T]GGAATCACAGAATAA | 51366 |
rs558618094 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102411274 | GCAGCATTGCGAACT[A/G]CAAACGTAAGAGTTT | 51366 |
rs558624195 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102336365 | TACACAAAGGTTTTT[G/T]GTTTCATGTAGCTCC | 51366 |
rs558647659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102367633 | TATAAACTGAGTCTT[C/T]GGCTTGTGCTGCATC | 51366 |
rs558651116 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102409137 | GCACTGAATGGTTTC[A/C]ATTCAGCTCAATGAA | 51366 |
rs558662220 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102396619 | AGATATATCTAAATT[C/T]AAATATATATATATA | 51366 |
rs558681481 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102410313 | TACATAAAGTTAGGA[A/C]TAATATAGAAAACAT | 51366 |
rs558701585 | in-del | -/AAAA | 0.00573031 | 0.0532195 | intron-variant | UBR5 | GRCh38.p7 | 8:102361216 | GGGTGGCTGAGAGAT[-/AAAA]AAAGAAAAAGTTAAA | 51366 |
rs558716007 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102375482 | TCCTGCAAAATAATC[A/C]CCCATAGGCTACATT | 51366 |
rs558718302 | in-del | -/CACT | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102378602 | GAGCCAAGATCGCGC[-/CACT]CACTGCACTCCAGCC | 51366 |
rs558745554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102257322 | AAAAGGATTAAGGAT[A/G]TATACAGGGAGAAGC | 51366 |
rs558748744 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102296045 | CTAATTCCCAGTCCT[C/G]TTCAAGTGGTCCTCC | 51366 |
rs558774372 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102309263 | TTTCGCTATGTTGCC[C/T]AGGCTGGCCTCAAAC | 51366 |
rs558778193 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102397195 | ACCAGTCCCCACATC[C/G]TGCAACCTAGTCTTC | 51366 |
rs558810687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102330075 | ACATGCAATGATTTG[A/G]AATGCAATTAAATTA | 51366 |
rs558813249 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303224 | ATTTTGTTTAGTCTA[C/T]GTAAAGTTTTTGCAC | 51366 |
rs558840463 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102397421 | AATCTAGCCTGGTGC[A/G]GTGGCTCACGCCCGT | 51366 |
rs558871790 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBR5 | GRCh38.p7 | 8:102344884 | CAGTGAGCCGAGATC[A/G]TACTACTGCATTCCA | 51366 |
rs558874296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102269795 | AGCATGCAAGGAAGG[C/T]AGAATGGAGACAGTG | 51366 |
rs558879627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303935 | GGAGGAACAAAAATG[A/G]AACAAAAAAGGACCC | 51366 |
rs558883065 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102399129 | TGAGTTGTATCATTT[-/A]CTCAAGGTCATATCA | 51366 |
rs558894556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102389034 | GTATCAGTCTTTTCT[A/G]AAACATTCATAGTAC | 51366 |
rs558911155 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102389520 | CAAGTACTGTCAATT[A/C]CCAGAAGAGATAATA | 51366 |
rs558914628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102403784 | TCCCAGGTCAAGCAA[C/T]GAAAATACTACTTTT | 51366 |
rs558917726 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102313861 | TTCCCGAAGAGACCA[C/T]TGCTCTTCATTCACC | 51366 |
rs558923748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102286687 | CAATGTACCCCCTCA[C/T]TCAGGAAAACATACA | 51366 |
rs558957458 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102389860 | TGCCTCCTGGGTTCA[A/C]GCCATTCTCCTGCCT | 51366 |
rs558961353 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102406964 | CACTATCCAAGAGAA[C/G]TTTCAGTGATGATGG | 51366 |
rs558962917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102268815 | ATGAGAAGAAACTAA[A/G]CTGTCTCATTCATGG | 51366 |
rs558971674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102337264 | AATCTGGATGTCTTT[C/T]ATTTCTTTTTCTTGT | 51366 |
rs558990836 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303982 | GACAGGTAAGAGATA[C/T]ACTGCTTTCTGTACT | 51366 |
rs559008300 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102414191 | CTCAAAGGTTTCTAT[G/T]ACCTCCTTTAAAAAA | 51366 |
rs559022558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102256383 | TATACCAGATAGCCA[A/G]TCCTTTCTGTTTTTG | 51366 |
rs559034858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102345549 | ACATAAGATCCTCTA[C/T]AAACAGAAACAAACA | 51366 |
rs559037317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102308798 | CATTTTTTAAAAAGG[C/T]AGTAAAAAATTTTAA | 51366 |
rs559060732 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102313042 | AGACAAGCACAGAAT[G/T]TGAAACCAGGACAAA | 51366 |
rs559070846 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102394341 | CTGGGGTTACAGGCG[C/T]GAGCCACCGCATCCG | 51366 |
rs559096167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102387064 | CTCCTTCAACTCAAA[C/T]TGCTTCCCCAACAAC | 51366 |
rs559128262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102359255 | TTAACTGGGTATTTT[C/T]AGAAAATCTGGCCAT | 51366 |
rs559135993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102298610 | TCACATATAAATATA[C/T]ACCTCAATCAAACTA | 51366 |
rs559138013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102308001 | AATAAACAACTCCCA[A/G]GTAAATTTCTCCAGC | 51366 |
rs559159661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102283864 | CCCTGCTACTTAATC[C/T]CTCAACAAGGCCCTA | 51366 |
rs559160441 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102400771 | AATTTTTCCAATTTC[A/G]TGGTTAAAAAAAAAG | 51366 |
rs559178798 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102285919 | TAAACCACACTATTT[G/T]GGGGAGAGGAGTATG | 51366 |
rs559203186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102408797 | TGAGACAGCAGAACC[A/G]TTCTGGAATACAAGC | 51366 |
rs559216135 | in-del | -/AACTT | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B, nc-transcript-variant | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102251976 | TCAAGGGATTATCTC[-/AACTT]GAGTTTAAACATAGG | 51366 |
rs559218241 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102408010 | AATAAAAAATGTCTC[C/T]AGACACTGCCCAATA | 51366 |
rs559234491 | snp | C/T | 1.64779e-05 | 0.00287031 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102342554 | ATCCAAGTTTGGCTC[C/T]CCTTCCTTGCTGGTA | 51366 |
rs559260375 | in-del | -/AC | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102362288 | GTTTCTCTTAAGAAA[-/AC]AGTCTTGAATGTAAA | 51366 |
rs559265953 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102381440 | CATGGGGGAAACCAC[A/C]CCCATGATCCAATCA | 51366 |
rs559274738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102319092 | CACATAACAATATTA[A/G]CTTTAAATGTAAATG | 51366 |
rs559275568 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | UBR5 | GRCh38.p7 | 8:102301017 | TTGTAAATGGATAAA[A/G]AGTAAAAATTTCATT | 51366 |
rs559321579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102263435 | TCTATTCCATTTGTT[C/T]TGTGTCAAGTAATTT | 51366 |
rs559330490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102355730 | TACAGTATTGCAATC[A/G]TGGACCTAATGCTTA | 51366 |
rs559336424 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102287671 | AAGAAGGCATAGGGG[A/G]TAGGAGTTGGGGAGA | 51366 |
rs559357816 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B, nc-transcript-variant | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102252132 | CCATTTTACTGGATA[A/G]TCTTGGTATCCAGAT | 51366 |
rs559360273 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102369825 | AAGAAAAGCAAAGAA[A/T]ACAATGACAATTAGT | 51366 |
rs559386224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102400096 | CCCTCTGTACCAATT[C/T]TGCATCTTCTTTTGA | 51366 |
rs559466911 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102343330 | ACCAAAATGCTTCCC[A/G]TGGCTATTGGCCTAC | 51366 |
rs559477104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102327562 | ATTCACTAAGTATGT[A/G]TTTTTATAAATTTAA | 51366 |
rs559519548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102398712 | CTTGAACCCAGGAGG[C/T]AGAGGTTGCAGTGAG | 51366 |
rs559536518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102334725 | ACACGGTGAAACCCC[A/G]TCTCTACCAAAAATA | 51366 |
rs559538438 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102326960 | GGCTACAGTGCAGGT[C/G]GCTGATCTCAGCTCA | 51366 |
rs559543751 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBR5 | GRCh38.p7 | 8:102351151 | TTCCTCAAAACATTA[A/G]AAGAACTACCATATG | 51366 |
rs559560900 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102390524 | ATACAACTGACAGGC[C/T]AACTCTCAACAATCA | 51366 |
rs559566384 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102386044 | CATAGTCCACCATCT[C/T]ACACCCTAGCATGTA | 51366 |
rs559568471 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102350898 | GACGTGAAATGATAT[C/T]TCTCCAAACGTGATA | 51366 |
rs559576363 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102385578 | ACTGTGTTGCCCAGT[A/C]TGGAGTGTAGTGGCT | 51366 |
rs559609218 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102371394 | AGACTATGGACGCAT[C/T]CCACCATGGCCAGCA | 51366 |
rs559615129 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102260520 | ACTCCGCCTAATGTT[A/T]GTTTCTTCCCCTGCT | 51366 |
rs559619794 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102253747 | TAGAGCTCAATGCAG[C/T]CAAACCGCAATAAAA | 51366 |
rs559622721 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102262523 | TTAAACTTGGGTCTA[C/T]TTAATTAGCTGTTTC | 51366 |
rs559623604 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102316709 | TCCCTCTTGAGTACA[A/T]TAATCTGTAAAACCC | 51366 |
rs559639056 | snp | A/G | 1.66657e-05 | 0.00288662 | intron-variant | UBR5 | GRCh38.p7 | 8:102313958 | CCAAAAAGAAAATGT[A/G]AAAGAGACTTTATAG | 51366 |
rs559649854 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102284962 | GAATGGCATGAACCC[A/G]GGAGGCGGAGCTTGC | 51366 |
rs559650824 | snp | C/G | | | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102280455 | AATACCCAGTTCCAA[C/G]AGTTCTCGCGTCCTT | 51366 |
rs559693998 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102282429 | ATCCCAGTACTTTGG[A/G]AGGCCAAGGTGGGTG | 51366 |
rs559712198 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBR5 | GRCh38.p7 | 8:102353866 | CTGTCAAAACCCAGT[C/T]TCCACAAAAAAATAA | 51366 |
rs559730753 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102309092 | GAGTCTCACTCTGTC[A/G]CCCAGGCTGGAGTGC | 51366 |
rs559803350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102305948 | TGTTGCCCAGGCTGG[C/T]CTCAAACTCCTGGGC | 51366 |
rs559816119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102392137 | AACATTCTATCAGTA[C/T]ATGTTACCAGTGTGA | 51366 |
rs559830615 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102340431 | ACCTACCTCTCTATT[C/T]CCTATCAAGCCTTCC | 51366 |
rs559838267 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102317710 | GGGGCAGACTGACAC[C/T]TCACACGGCCGGGTA | 51366 |
rs559893407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102405480 | GCCAAGGAGTCAAAA[C/T]GACAGAAACATGGAT | 51366 |
rs559893493 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, nc-transcript-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102412910 | GGTCCGTTCGGCTCC[C/G]GAGCCCAGCCCCGCC | 51366 |
rs559894979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102288116 | TTTAAAAGTACCTGA[C/T]TTACTCATACTGAGT | 51366 |
rs559929885 | snp | A/C | | | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102298408 | TTTTGCAATTTTCTG[A/C]GCAGTTTCTAAGATG | 51366 |
rs559961940 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102370557 | GGATTTCACCTCAAA[C/G]ATTTATCATTTGTGA | 51366 |
rs559984304 | snp | A/T | 1.64963e-05 | 0.00287192 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295512 | ACTGTCTGTACTAAG[A/T]ATAGTAAGAGGTGCT | 51366 |
rs560029156 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102349087 | AGAAAAGCAATATAA[C/T]GCATCCTCAAGGCTG | 51366 |
rs560057785 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102339118 | ATTTAATTCAAGAAT[A/G]ATTTTGGGAAATATG | 51366 |
rs560059827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102288626 | TGCTTGAACCCGGGA[A/G]GTGGGGGTTGTAGTG | 51366 |
rs560062767 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102332925 | AACAAATGAATCTTA[A/C]CTCCAGCTTCTTTGG | 51366 |
rs560064406 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102324264 | GGCTCCATAACTTTA[C/T]AGATGTTTCTTTATC | 51366 |
rs560067204 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBR5 | GRCh38.p7 | 8:102317502 | TGTAGGCTCCACCTC[C/T]GGGGGCAGGGCACAG | 51366 |
rs560073861 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102375876 | AACATGAAAATTATA[C/G]GAAGTCCGATCACTG | 51366 |
rs560082418 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102297794 | CAATATAAAGTAAAG[C/T]ATAATTACATCATAC | 51366 |
rs560119706 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102306441 | ACACAAGAAAACACA[C/T]CTAAACAACTATTTT | 51366 |
rs560119764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102297140 | GGGCTACAGCAAATA[C/T]ACAGTTTATGATATA | 51366 |
rs560155540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102280931 | AGATTACTTGAGCCC[A/G]TGAATTCAAGGTTGC | 51366 |
rs560162076 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102279894 | CATTTGAAATAACTG[A/C]AACCCACAAATAAAC | 51366 |
rs560169299 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102293482 | TCCGGCTTTCTGGTT[-/G]TTATTTATGTTACAC | 51366 |
rs560191281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102279443 | AAATTTTACGTTATG[C/T]GTATGTTACAATAAA | 51366 |
rs560234501 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102391395 | AGAAAAATGAATATA[C/T]ACTGAGTATTGGATG | 51366 |
rs560258897 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102323013 | GTTAATGGGTGCAGC[A/T]CACCAGCATGGCACA | 51366 |
rs560329653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102375265 | ACTTGGGAGGCTGAG[A/G]TACAAGAATCACTTG | 51366 |
rs560332413 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303407 | ATGGAACAGAAAATA[C/G]GCAAGGAGAATCTTC | 51366 |
rs560416113 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102301354 | TTGGAATAAAAACAC[G/T]CTAGAAGATTCTGCA | 51366 |
rs560426718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102410557 | CAGAATTTAAAGGAA[C/T]TATGTGACAACTCTG | 51366 |
rs560522066 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102338233 | GTTGATGTTTTGGGG[C/T]AAAAACCTTCAGAAA | 51366 |
rs560535511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102256678 | GTTAGGACTGCTGAA[C/T]AAACCCATCTCACCA | 51366 |
rs560552922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102331113 | TTGTATAAATACAGT[A/G]TATACTACATATAAC | 51366 |
rs560554830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102404112 | CCTAAAATGGGTTAA[C/T]TTTACTGAATGTAAA | 51366 |
rs560557743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102358856 | CATGGCTCACTGCAG[C/T]CTCAACTTCCTGGGC | 51366 |
rs560579957 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102266479 | CCTTATGCTATAGCA[C/T]GATATGTCACTTGTT | 51366 |
rs560590162 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102374836 | ATACTCAAACTACTT[A/G]TACAATCAAATATCT | 51366 |
rs560616890 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102330398 | ATAACACAATAACAA[C/G]AGGTTATGCCTTAGT | 51366 |
rs560618742 | snp | A/C | 0.0573587 | 0.15934 | intron-variant | UBR5 | GRCh38.p7 | 8:102322513 | TAAACTAGTTCAACC[A/C]TTGTGGAAGTCAGTG | 51366 |
rs560655566 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102286731 | GCCAGATTGTATTCA[A/G]TAATCCACAAAACCT | 51366 |
rs560664101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102354101 | ACATGTATGCACACA[C/T]AAGTCTGAATGATGT | 51366 |
rs560676231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102353546 | AAAGGGTGACTAAAT[A/G]TAAAGTGGAATCCTG | 51366 |
rs560676477 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102360870 | AAATAATTTACAACA[G/T]CTCAATCTGACAAAA | 51366 |
rs560682232 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102369078 | TATTTGACAAGGGGG[A/G]CTGTTTTACATTTTT | 51366 |
rs560694504 | snp | A/C/T | 0.000165926 | 0.009107 | intron-variant, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102258966 | TTCATTCTTTAAACA[A/C/T]TTTTTTTAAATGTCC | 51366 |
rs560720603 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102401190 | ACTTTAAAAAAGCTT[A/C]ACCATATCATGTCCC | 51366 |
rs560725007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102259848 | GGCAGATCATGAGAT[C/T]AAGACCCCGTCTCTA | 51366 |
rs560757516 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102264132 | TTTGCCAGGTACTTA[C/G/T]GATGTTGTGTTTCTT | 51366 |
rs560769218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102396942 | CGATCTCCTGACCTC[A/G]TGATCTGCCCATCTC | 51366 |
rs560807104 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102388551 | GTAACGTGCTGATGA[C/T]GTCATAACAAGATTT | 51366 |
rs560827453 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102321096 | TGGCCAGGGCAATTA[C/G]GCAGGAGAAGTAAAT | 51366 |
rs560834618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102403318 | TGGAGAGGCTGAGAC[A/G]GGATAATTGCTTGAG | 51366 |
rs560841871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102271699 | TATGGTTTCCTATAA[A/G]TGTACAAAACAGATA | 51366 |
rs560870067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102395281 | CTGTAACTGTCTCTT[C/T]TTCATGAACCAAACA | 51366 |
rs560900254 | in-del | -/A | | | utr-variant-3-prime, downstream-variant-500B | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102252323 | TTTTATGATTTACTT[-/A]AAAAAAAAAATCTTT | 51366 |
rs560905083 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102343277 | GAGGAACCAGACAGG[A/C]TTTTTTTTAAAAATA | 51366 |
rs560913384 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102276173 | TTTCACCATGAACCA[C/G]AATCTCCATTTGTTA | 51366 |
rs560920070 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102315467 | ACATAAATATTTTTA[C/T]ATATTAAAGGGTAGA | 51366 |
rs560921952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102308326 | CCAAAACCATTAACC[C/T]TCTTGCTTCGTCTAT | 51366 |
rs560934722 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102352070 | CCCAGCACTTTGGGA[A/G]GCTGAGATGGGCGGA | 51366 |
rs560950199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102345018 | TTTTTTCACATTTCA[C/T]TATTTTATCTAACCA | 51366 |
rs560965951 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UBR5 | GRCh38.p7 | 8:102342409 | TAAATAAAATGGAAA[C/T]CTTAGAGGGAGGGGT | 51366 |
rs560971802 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102401364 | AATACCAACTGTCCT[C/T]GAGTCCCTGCCACTC | 51366 |
rs561045447 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102392346 | AATTTACTGAATCTA[A/G]AAGGTACTATCTACC | 51366 |
rs561063435 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102279675 | AGTAATGTCTGAGCA[A/G]TTTACATATCTCAAT | 51366 |
rs561077527 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102307166 | TGGAGCAACAAACTC[A/T]AAGTAGTGAGAACTG | 51366 |
rs561090607 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102336123 | TTCCCTGACAATTAC[A/T]GATGTTAAGCACCTT | 51366 |
rs561097672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102291667 | TTTTGGAGAGTTTTG[A/G]ACTGCACTCTACACT | 51366 |
rs561127233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102365187 | ATAACCTCACTGGCC[A/G]GGCACAGTGGCTCAT | 51366 |
rs561134385 | snp | A/G | 0.00874735 | 0.0655527 | upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102412762 | AGGGGCAAACGGGAG[A/G]AGGAGGAGGGAGGAG | 51366 |
rs561158565 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102301604 | TCCTTACCAGTAACA[G/T]CACACACCATGGTGA | 51366 |
rs561167167 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102367141 | AAAAGACAACCTATC[-/T]TCTAACCACAGAACA | 51366 |
rs561227228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102292840 | TAAAGGAAAAATTGG[A/G]ACACATATACTGGCA | 51366 |
rs561264019 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102300502 | AAGTTTCTATCCCCC[A/G]TTTATAATCGGTAAT | 51366 |
rs561273983 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102344392 | CACCTCAGCTCACTG[C/G]AAGCTCTTCCTCCCG | 51366 |
rs561290952 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102335467 | ATAGATGTGTTAATC[C/T]ATTATAGTAACAATA | 51366 |
rs561372700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102254978 | AAAGCAAAAAAAGTA[C/T]TTACTGCTACATTGT | 51366 |
rs561392630 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102387499 | GATCACTTGAGCCCA[C/T]GAGTTCGAGATCAGT | 51366 |
rs561436805 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102400077 | GGTGATGGATCCATG[C/G]TACCCCTCTGTACCA | 51366 |
rs561470200 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102350345 | ACAAAGCTGAAGTAT[A/T]TAAAACAGTATGGGT | 51366 |
rs561494879 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102270945 | TTTTAAAGCAGAACT[G/T]TTTATTAGTTAATAG | 51366 |
rs561501601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102306787 | ACCTGCCAGACTATA[A/G]TAGATGGGCTCTCAC | 51366 |
rs561503154 | snp | A/C/T | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102320099 | AAAATCAGAGCAGAA[A/C/T]TGAAGGAAATAGAGA | 51366 |
rs561511061 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102384894 | AAACTAAATCAAGAG[C/T]TTTAATCTGAAATAC | 51366 |
rs561513636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102277317 | GAGCTTCAATGGTCC[C/T]TTTGTCTGATGGCCC | 51366 |
rs561563350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102306702 | GGTGCTGTCATATAC[A/G]CTGGTTTCAAGTAAC | 51366 |
rs561582438 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102377839 | GCCTTGTTTTAGGAG[A/G]CAGCAATAGATTTCA | 51366 |
rs561583764 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102380001 | TGAAAATTTTAACAG[A/T]AACCATTAAAATAAT | 51366 |
rs561585568 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102387441 | GGTCAGGGGTGGTGG[A/C/T]TCATGCCTGTAATCC | 51366 |
rs561610584 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102326159 | GCCAAAGCCCCCTGC[A/C]TCATGCTGACAACAT | 51366 |
rs561612666 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102397309 | GTCTCCTCATCAAAC[C/T]GAAAGCTCCATGAGG | 51366 |
rs561652592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102371068 | TGTGACTAGTGCTGC[A/G]ATAAACATCTCTTAA | 51366 |
rs561658089 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102414116 | CATCTCAAAAAAAAA[A/T]TTTTTTTAATCAAAT | 51366 |
rs561685698 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102276119 | AGTCCAATGTCTATC[A/T]CCATTTAGGTGACTC | 51366 |
rs561693864 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | UBR5 | GRCh38.p7 | 8:102326888 | ATTTTATGGGAAATT[C/T]ATCAATTGCTTTTTT | 51366 |
rs561711205 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102370517 | ACATGTATACAATGT[G/T]TTAATAATCAAATCA | 51366 |
rs561727736 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102349481 | GATTGTGCCACTGCA[C/T]TCCAGCCTTGGCTAC | 51366 |
rs561740304 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102356542 | AGGCAGTTGGATCAC[A/G]AGGTCAGGAGATCGA | 51366 |
rs561743514 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102311563 | TGATTTTTACAGGCA[A/T]ATTTATTTCCAAATT | 51366 |
rs561761215 | in-del | -/CAACATAATGAGACCCCGTCTCTA | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102384513 | TGAGACTAATGTGGG[-/CAACATAATGAGACCCCGTCTCTA]CAAAAAATTTAAAAA | 51366 |
rs561763423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102378398 | CCTGTAATCCCACCA[C/T]TTTGGGAGGCCGAGG | 51366 |
rs561769783 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102334775 | TGGTGGCAGGTGCCT[A/G]CAGTCCCAGCCACTC | 51366 |
rs561775797 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102259901 | GGCATGCTGGCGCGC[A/G]CCTATAGTCCCAGCT | 51366 |
rs561782041 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102313513 | GGGCTGTACCAAAAA[C/G]TAACGTATCTCTATG | 51366 |
rs561810599 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102333703 | CATTTTTTCTACTAT[A/G]AGCAAACACTGGTTT | 51366 |
rs561819000 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102319059 | TAACCAGCTAACATC[A/G]TGACAGGATCAAATT | 51366 |
rs561821343 | snp | A/G | 0.00020016 | 0.010002 | intron-variant | UBR5 | GRCh38.p7 | 8:102361084 | CAATTCTATTTTAAC[A/G]GTTTATTTTTCATTT | 51366 |
rs561855342 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102262356 | ACTTTGCACTACTTA[C/T]TAAACACCAATTATG | 51366 |
rs561892049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102261816 | GTACACACACGTTCA[C/T]CTCTTTCATTCCCTA | 51366 |
rs561898623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102405229 | ATAGAGGAGAATAAA[C/T]GGGGAGAGAGTTGAA | 51366 |
rs561934520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102354937 | AGTTAAAGACCAGCC[C/T]GGGCAACATGGCAAA | 51366 |
rs561934850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102363665 | CCATTCCTTTGTTAG[C/T]AGCTCAAAACTTGTC | 51366 |
rs561955950 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102288802 | GGGCAGGGAGGAGAG[A/G]ATTTACCTCATAAAT | 51366 |
rs561975726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102391964 | TAATCCTCACTGCTA[C/T]ACTCCCAACAGTGCC | 51366 |
rs561986650 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102371847 | CTGCCTCGGCCTCCC[-/A]AAGTGCTGGGATTAC | 51366 |
rs562030845 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102306403 | CTATCCCCAACTTGA[C/G]AGCGGGTGGAGAACA | 51366 |
rs562038022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102268749 | ATGTACTTTCTTTCA[A/G]GTAATTTCCAAATAA | 51366 |
rs562047498 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B, nc-transcript-variant | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102251980 | GGGATTATCTCAACT[C/T]GAGTTTAAACATAGG | 51366 |
rs562062347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102266542 | GAATGAGTCCCAGGA[A/G]TCCTAGAACTCCTGA | 51366 |
rs562084954 | snp | A/C/G | 3.30449e-05 | 0.00406467 | intron-variant | UBR5 | GRCh38.p7 | 8:102311507 | GATTCCTATAATAAT[A/C/G]GGAAAATGGTAAAGT | 51366 |
rs562094539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102302754 | CGCCTAGAAAATCCA[C/T]TGGAGGCTAGAGGAG | 51366 |
rs562102579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102337817 | GTTGGTATAAACACA[C/T]ATATAATTACAATTT | 51366 |
rs562111066 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102340240 | TGCAACTGCTCTGGT[C/T]TTCCAGTGTTAGCCT | 51366 |
rs562121916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102310812 | TGAAGTTTAGGTAGC[A/G]TTAGGTGAACACACA | 51366 |
rs562166392 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102345915 | AAATACAAAAAATTA[C/G]CCAGGCGTGGTGGCG | 51366 |
rs562182626 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102272355 | ATAAATGTGTCCGTA[C/G]AATAGCAAATTGTTG | 51366 |
rs562207856 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102317233 | AATCGGGCCACTCCC[A/C]CCTGAATACTGCGCT | 51366 |
rs562216869 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102325148 | CTACAAAGGAGGGAA[G/T]GAGGGGCAAAGAGAG | 51366 |
rs562220672 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102391493 | TCATACTTAGACGAT[-/A]ACAAGCACATGCATT | 51366 |
rs562233109 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102274499 | CACTTTGGGAGGCCA[A/G]GGCAGGTGGATTACT | 51366 |
rs562257808 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102361973 | AAGGCTCAATTGTTT[-/A]AAAAAACAAAACAAA | 51366 |
rs562277529 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102310156 | CTCTACCATCAACCA[C/T]GCCCAAATCAGAAGC | 51366 |
rs562315534 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102297040 | ATGCATATATCTCAT[A/C]ATAATAATTATTTCT | 51366 |
rs562327895 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102348174 | AGAGGTAGCAGCGAG[C/T]CGAGATCGCGCCACT | 51366 |
rs562329003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102368997 | AATAAAATTTGTGAA[C/T]ATTTTAAAAATAAAC | 51366 |
rs562350874 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102294714 | ATATTTTTCTGTTTT[A/T]AAATTTTACATTATT | 51366 |
rs562399520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102305863 | TCAAGTAATCCTCCC[A/G]CCTCAGCCTCCCATG | 51366 |
rs562407399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102405734 | TGAGGCAGCAGAATC[A/G]CTTGAACCCGGGAGG | 51366 |
rs562421201 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | UBR5 | GRCh38.p7 | 8:102274503 | TTGGGAGGCCAAGGC[A/T]GGTGGATTACTTGAG | 51366 |
rs562441544 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102287022 | CAACTCTTTAAAAAA[A/T]AAAATTAGCCCGATG | 51366 |
rs562484592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102338403 | AAAATGTTTTCATAA[C/T]TTGAATTCATTCTAG | 51366 |
rs562493129 | in-del | -/C | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102276470 | CTATTAGTAATAACA[-/C]AACAGCTTTTTAGCT | 51366 |
rs562495012 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102331504 | GTTTTCCTCCCCTCC[-/T]ATTTAAAGATAACCC | 51366 |
rs562502484 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102273963 | GTTCACTCTGCCACA[C/T]TGTAGATATTTTACA | 51366 |
rs562510031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102321258 | CAGGATACAAAATCA[A/G]TGTACAAAAATCACA | 51366 |
rs562577150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102258870 | GTTTTAATGCTTGAG[C/T]AATACAGCAATTTCC | 51366 |
rs562589009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102286061 | TATCACAACTGTGGG[A/G]GCCAAGGGGAGGGGA | 51366 |
rs562620529 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102326381 | ATACTGAACCACAAT[C/G]TATACAGTATTACTC | 51366 |
rs562621523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102332169 | AGGAAGAGATGAGGC[A/G]TGCTCCCAGGTTCCC | 51366 |
rs562634846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102302153 | TCTTCATTAGGTCTT[A/G]GGAACATTTTTAAGT | 51366 |
rs562659797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102277858 | AATAATTACCCATGC[A/G]TGGTGGCGGGCACTT | 51366 |
rs562707317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102330253 | ACTTCTCCATTTTCT[C/T]TGGGATTCTGGCTCC | 51366 |
rs562717910 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102327671 | TCTCATGTTGGTATT[A/C]CACTACTCAAAGCAT | 51366 |
rs562718159 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102280728 | CAGAAAACATGGGCT[A/G]AGCATGGTAACTCAT | 51366 |
rs562754331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102287953 | AAGAAACTGACTTAA[A/G]AAGAAAAAAGGGAAA | 51366 |
rs562781894 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102381597 | ACACTGACAAAGAAC[A/G]TTAATAACCTTTCTC | 51366 |
rs562817815 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102382908 | TGTATTCAGAGAAAA[C/G]AGGAATAATTTTCCT | 51366 |
rs562818427 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102266793 | TCTATGCATAATACC[A/G]ATATATTTATCTTTG | 51366 |
rs562855946 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102374714 | TAGTCTCAGGCCTAC[A/C]CTGAAACAAACTGTG | 51366 |
rs562880990 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102378636 | GTGACAAGAGTGAAA[C/T]TTGGTCTTGAAAAAA | 51366 |
rs562903294 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102410391 | GCACTACCAACATGG[A/T]TCTGTTAATGACCGT | 51366 |
rs562921041 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102351350 | GCTTTTAAAAGGAAA[A/T]CCTATCACATGCTAC | 51366 |
rs562933687 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102351077 | AGAAACTGGAACCCA[C/T]GTGCACTGTTGGTGG | 51366 |
rs562938111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102360256 | CTGTTATTTCAAATT[A/G]CATTGCTTAATTTGG | 51366 |
rs562981257 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102329622 | CCTTCTTCCTGTCAC[A/G]GTGGTCTTCTTCCTA | 51366 |
rs563015739 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102332937 | TTAACTCCAGCTTCT[C/T]TGGGTAAATGCCTTA | 51366 |
rs563039699 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102335996 | GTTCCCAACAGCATA[A/C]AAGGGTTCTCTTTTC | 51366 |
rs563044680 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102322394 | ACCACAATGAGATAC[C/T]ATCTCACACCAGTTA | 51366 |
rs563058555 | snp | A/G | 1.65211e-05 | 0.00287407 | intron-variant | UBR5 | GRCh38.p7 | 8:102272519 | TGCTTGTTATTTGTA[A/G]AGTACTTACTTGTGT | 51366 |
rs563066278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102402360 | CAATAATTGGACAAG[C/T]TCGAATTACTTCTGG | 51366 |
rs563067722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102265434 | AGGTAAATGAACTTT[C/T]AATTTGCCCTTTCAG | 51366 |
rs563107234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102264743 | GGAACACCAGCCTGA[A/G]AATGTTTTGTTTTTG | 51366 |
rs563118431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102309664 | AATGCCTACGGTATC[C/T]AGTACAGAAATACAC | 51366 |
rs563142199 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102401747 | CCCAAAAAACAACTA[C/T]AGAAACAAAAGGTCC | 51366 |
rs563154264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102291979 | TACTTAGGAAAGTTC[C/T]TAGTACATACTAAAA | 51366 |
rs563173519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102409705 | TAGATGAAAATACGC[C/T]TATTCTAGTTAATTA | 51366 |
rs563179226 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102378512 | AGCCGGGTGTGGTGG[C/T]GCACGCCTGTAATCC | 51366 |
rs563179257 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102404850 | AGGCGGAAGTTGCAG[C/T]GAGCAGAGATCACGC | 51366 |
rs563216205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102277266 | TCCTCAACTTAGTAA[C/T]ACAGGAATCATACGC | 51366 |
rs563231165 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102401222 | GATCCCCAAAAAATG[C/G]TATTACCTCTCAATA | 51366 |
rs563293280 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102350264 | TGAGGCAAGCCCAGA[C/G]AGCCAAAACAGTTTG | 51366 |
rs563297453 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102341369 | GGAAAGTTTGGCAGT[A/T]GCCAAAGAAAACAGA | 51366 |
rs563356341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102349217 | CATCAACAAAAAAAG[A/G]AAATTAAAAAAACAA | 51366 |
rs563363111 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102340491 | TACCCCTAACTAATT[C/T]TGAGAAACCAATATA | 51366 |
rs563373829 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102255262 | TCAGTGTCTGTCTCT[C/T]TTAAGGAAAAGCTTT | 51366 |
rs563376290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102319130 | TGCTCCAATTAAAAG[A/G]CACAGACTGGCAAAT | 51366 |
rs563406313 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102409430 | GGTAAAGAAAGAAAA[C/T]GTATTTGAAGAAAAC | 51366 |
rs563407916 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102385949 | CTAGTTAACTGTTCA[A/C]AAACTTTCTCACCCA | 51366 |
rs563427996 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102344199 | GTAAAAATATTGACA[A/T]TTATAATGTAAACAA | 51366 |
rs563444693 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBR5 | GRCh38.p7 | 8:102388173 | AAAATACTCTCTTAG[A/G]CACAGCTATGAAATA | 51366 |
rs563462410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102358775 | CTTTTCTTTTCTTTT[C/T]TTTTTTTTTTTTTGA | 51366 |
rs563462897 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102369649 | AAGTCTGAATAACCA[C/T]TATTTGTCAGTCAGT | 51366 |
rs563488276 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102337640 | TGGTCGTGATGTATA[C/T]CTTTTTGATATGTGT | 51366 |
rs563489690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102343580 | CATTTGGCCAGGTAT[A/G]GTGGCTCACACCTGT | 51366 |
rs563527633 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102371776 | GTATTTTTAGTAGAG[A/G]CAGGGTTTCGCCTTG | 51366 |
rs563560022 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102393040 | AAACGCTACATATTT[C/G]AAAAGTGTTTCATGC | 51366 |
rs563578646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102379140 | TACCTCCTCTCTCGG[C/T]TTCTGAAAGGGGAAG | 51366 |
rs563635095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102308207 | TGTCTTCACATTCAC[C/T]TCCTCTATCAGAAGA | 51366 |
rs563645684 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102298311 | CATATATAGAAATCC[A/C]GTCTGAATAATTATA | 51366 |
rs563669568 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102306071 | GATACCTTCAATTCT[G/T]CAGGGATCATGACAG | 51366 |
rs563676041 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102255003 | CATTGTGATACAGAA[C/T]CATTTTATAATAGTA | 51366 |
rs563682697 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102297836 | GCCAATACAAACACA[C/G]TATACATCAGCCATC | 51366 |
rs563700956 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102399992 | ACATGGGGAAAATGT[C/G]TCTATCTCTAGTATT | 51366 |
rs563718614 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102379795 | TTCACCCTGAGGAAG[A/G]CTTCTCCTACTCTAA | 51366 |
rs563726702 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102333444 | TTCAACAAAAAGAAG[C/T]TGAATCAGTAAATCT | 51366 |
rs563734895 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102253845 | CCATATACATGATAC[A/T]CAGTTGCAGCCAACC | 51366 |
rs563742552 | snp | A/C | 1.66657e-05 | 0.00288662 | intron-variant | UBR5 | GRCh38.p7 | 8:102289404 | CTACTGACTACTCTT[A/C]TTTTCTCATAAAATA | 51366 |
rs563756417 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102403537 | GGCAATAGCGCAAGA[A/G]CCTGTCTCAAAAAAA | 51366 |
rs563762139 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102399337 | TAGAGTGCAATGGCG[A/C]GATCTCGGCTTACTG | 51366 |
rs563766820 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102349552 | AAAGGGAGGGGAGAG[A/G]GGAGAGAGAAGAGCA | 51366 |
rs563800241 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102306529 | AAGTCACCTCATCAA[A/C]AGCAAGCTCCAGTTC | 51366 |
rs563811465 | snp | A/C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102372167 | CAGATTTCAGCTTGC[A/C/G]CATTGATCCCTGTTA | 51366 |
rs563812401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102283161 | ACAATGAAATGTTAC[C/T]AGGAAATGAAAAAGA | 51366 |
rs563829566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102288717 | ATAAAAAAATTATAC[C/T]CACAGATCCCAAAGT | 51366 |
rs563840312 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102386206 | AGGCCAAGGCGGGTG[C/G]ATCACCTGAGGTCAG | 51366 |
rs563841691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102312792 | CATCTCCTAATTAAA[C/T]TAAAGCAGCCTTCGG | 51366 |
rs563896074 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102258189 | CTAAATTTTTGGTTT[A/G]TAAATGAGACAAATT | 51366 |
rs563952768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102283958 | AACTATTACCTCTAC[C/T]GTAGATGCCTATCAC | 51366 |
rs563955856 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102290822 | TAATTTAAAAATACC[A/G]ATACATAAAACGTAT | 51366 |
rs563987831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102334744 | CTACCAAAAATACAA[A/G]AGACTTAACCGGGCA | 51366 |
rs563990453 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102307004 | CTTCATCCCTACCTG[C/T]GGGATGATGACTCTA | 51366 |
rs564000245 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102317727 | CACACGGCCGGGTAC[A/T]CCTCTGAGACAAAAC | 51366 |
rs564062372 | in-del | -/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102385058 | AGCCTAGTACAAAAT[-/C]GTTAGCTGCTCCTGC | 51366 |
rs564064800 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | UBR5 | GRCh38.p7 | 8:102339507 | ATACTCCAACCTGGG[A/C]AACAAGAGCGAAACT | 51366 |
rs564075268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102333543 | GTTAAAAATATGAGA[C/T]ATGAAATAGCGGCCA | 51366 |
rs564075525 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102282248 | GTACTTTCAAGGATA[C/T]CACCAAGAAAGTGAA | 51366 |
rs564091427 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102300915 | AATAAAACCTTACAA[C/T]GGCTACAAAATTAAT | 51366 |
rs564094143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102266424 | AATTGGAAGTCTCAC[C/T]TTCTATGTGCAATTG | 51366 |
rs564108944 | snp | G/T | | | upstream-variant-2KB, nc-transcript-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102412991 | AGGAGGAGGCTGCGG[G/T]CTAACCTGCCGGGAG | 51366 |
rs564109021 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102376963 | TAGGGGTCTGTTTAG[C/G]GAGGCAGTAAGTAAG | 51366 |
rs564158708 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102385429 | TTAGAATTACCTCTA[A/T]CCCACCCAAGTGACC | 51366 |
rs564182034 | in-del | -/CA | 0.197978 | 0.250301 | intron-variant | UBR5 | GRCh38.p7 | 8:102261699 | AGCAAGACTCCATCT[-/CA]CACACACACACACAC | 51366 |
rs564182961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102340108 | ACCTCACAAGTTTCA[C/T]AAGACAGGCTCAATA | 51366 |
rs564206351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102375796 | ATAAAAGCCTATTAT[A/G]GTGCAGAGCCTGGCT | 51366 |
rs564220156 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102273607 | TAGCAAAAAAAAACA[A/C]GAGGCCATTCATCAC | 51366 |
rs564227354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102268708 | ATGGCCTTTGCCAGG[A/G]GGGTATTCTGATAAG | 51366 |
rs564231318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102261318 | AGCAGTAAAACATTA[C/T]TGTTTATAAAACTAG | 51366 |
rs564246371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102365358 | TAGTCCCAGCTACCC[A/G]GGAGGCTGAGGCAGG | 51366 |
rs564289912 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102411458 | AATGCACTTCCCCAC[C/T]CCCGCTTGAATCCAT | 51366 |
rs564312425 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102360979 | TAAGCTTTCTCTGGG[A/C]CAGAGGAGGAAAGAG | 51366 |
rs564313337 | in-del | -/TT | 0.00419831 | 0.0456238 | intron-variant | UBR5 | GRCh38.p7 | 8:102269154 | ACTCTCTAAAACCTC[-/TT]GTCTAATTACATCTA | 51366 |
rs564315210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102268018 | CTGCCTCAGCCTCTC[A/G]AGTAGCTGGGATTAC | 51366 |
rs564324884 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102368902 | ATCTCAAGACCACCT[A/T]ATACTCTTAAAAACT | 51366 |
rs564337399 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102370408 | CCGAACTCAGGTGAT[C/G]CACCCACCTCAGCCT | 51366 |
rs564381914 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102399065 | AGGGCATGGAAACAG[C/G]AGTTAAAAAAAGACC | 51366 |
rs564385889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102275253 | AAACAAAAAAATTCA[C/T]AGAGGATGCTAGGGA | 51366 |
rs564419025 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102263870 | AGCTGGGACCACAGG[C/T]GCATGCCACCACACG | 51366 |
rs564420336 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBR5 | GRCh38.p7 | 8:102322856 | CAAAAAACCAAACAA[C/T]GCATATTCTCACTCA | 51366 |
rs564437101 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102314144 | TTTAATTGTATTAAC[A/G]CCAGTATAAACAAGT | 51366 |
rs564437625 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102404939 | AAAAAAAGTTACAGC[A/G]CTGAGCTTTAAGGAA | 51366 |
rs564442093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102404202 | TTGAACAAATAACAG[C/T]ACTTTAGCTGTGCAA | 51366 |
rs564454898 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102316439 | CTGGTCACCTATTTT[C/T]ATAAGATTAAGAAAA | 51366 |
rs564491610 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102345199 | ACATCAATTCCACAA[C/T]GTAAATAGGATCAAC | 51366 |
rs564495608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102353316 | ATCAAATTAATCCTA[C/T]AATTTTGATCCCGTT | 51366 |
rs564533240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102316948 | AATATGAGGGGGGAG[A/G]AGCCAAGATGGCCAA | 51366 |
rs564542433 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | UBR5 | GRCh38.p7 | 8:102309215 | AGGCACAACCACACC[C/T]GGTTAATTTTTGTAT | 51366 |
rs564559920 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102323947 | CCAGCCTGGGCAACA[C/G]AGTGAGACTCCATCT | 51366 |
rs564572263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102323092 | CTTAAAGTATAATAA[C/T]AATAAATTAATTAAT | 51366 |
rs564584898 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102280577 | AAGGTCGCTAATGTA[G/T]CTAACCAATTTCAAA | 51366 |
rs564657237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102337114 | AATACTACTGATTTT[C/T]GTATGTTGACCTCGT | 51366 |
rs564663460 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102310713 | CTCTCTAAACACCCA[A/C]CAGCCACTGCTGATC | 51366 |
rs564715132 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102375334 | TCCCTGGCACCCTAG[C/T]TTGGGCAACAGAGTG | 51366 |
rs564716858 | snp | A/G | 0.000214145 | 0.0103454 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102305189 | CTGATGAATGTCTGC[A/G]GCATCTGTAGATTCT | 51366 |
rs564723277 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102383646 | CATACATCCAACCAC[C/T]AGGAATTCCAAAAAG | 51366 |
rs564752974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102311226 | CTATTTAAGATTGTT[A/G]CAAGATCTATTCAAG | 51366 |
rs564764232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102257515 | TATTTGTGACCTTCT[A/G]TAATTGCCCTACCCA | 51366 |
rs564786158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102382774 | AGAACCACAGATACA[C/T]GAGCAGAGATTATGA | 51366 |
rs564795424 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102354331 | AAAATGGGGAATCCA[A/G]TTTGTCAGAATCCTG | 51366 |
rs564810255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102412011 | GGATGAGAAGTTTGC[C/T]CCGGAAGGAGCCTAG | 51366 |
rs564830894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102361913 | AGCTTCTAGAGTTTA[C/T]AGAAAAGGTAGCATA | 51366 |
rs564861267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102359748 | GAATAAGTTGTACCA[A/G]GAATAAGTTGTAAGA | 51366 |
rs564863454 | in-del | -/AACA | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102259408 | AAAAGTTTTGTTAAT[-/AACA]AACAGGCTAGTCATT | 51366 |
rs564876011 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102345878 | CCATCCTGGCTAACA[A/T]GGTGAAACCCCGTCT | 51366 |
rs564929434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102396206 | GGTCTGAGGCAGGAA[A/G]TAAGAATCAAACCTT | 51366 |
rs564937126 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102286916 | GGGTGTGGTGGCACA[G/T]GCCTATAATCCCAAC | 51366 |
rs564969975 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102402253 | ATGTTTATAAACTAC[A/T]CTCACCCACAATTTC | 51366 |
rs564982040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102401480 | TCTGCAGGCAAGTGT[C/T]GTATGTACTCTTCAG | 51366 |
rs564992749 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102390065 | CGCCCAGCCAAGAAG[A/G]ATTATTTTTTAAAAA | 51366 |
rs565011003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102337700 | GGATTTCTGCATCAA[C/T]GTTCAAAGATATTAT | 51366 |
rs565013552 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102304805 | CTTAACCTGCTAAAT[A/G]ATTCTCATGTAATAA | 51366 |
rs565013755 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102256818 | ATGAAGGTAACTGGG[A/C]ATCTGCAATTTTTTT | 51366 |
rs565065166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102299325 | GGAATGTAATTCAGA[A/G]AATTAGATGTTTTTC | 51366 |
rs565093991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102335865 | AAGTGCAGATATGCA[C/T]GATTTCATCTCCTCT | 51366 |
rs565112793 | snp | C/G/T | 0.00159649 | 0.0282165 | intron-variant | UBR5 | GRCh38.p7 | 8:102373175 | AAGCAAAATCAATCA[C/G/T]GTTATTTTCAGCTCC | 51366 |
rs565166036 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102294591 | GTTTGGTTGTTTGGT[G/T]TTTTTTTTTACGTTA | 51366 |
rs565177701 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102286235 | CATATGTACATATTT[G/T]TTATATTTGAAACTC | 51366 |
rs565182242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102388456 | ACATGTCTCTGAAAA[C/T]AGAAAACATTCAGTC | 51366 |
rs565196423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102395088 | TAACACCTTGTCCTA[C/T]GTCCTACATCCTACA | 51366 |
rs565208601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102389420 | CAGACCCCAGTTGTT[C/T]TGAGTCTTTAAATGA | 51366 |
rs565222182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102337006 | TCTCGCCTCAGCCTC[C/T]CAAAGTGCTGAGATT | 51366 |
rs565225649 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102321175 | AGATGACATGATTGT[A/C]TATCTAGAAAACCCC | 51366 |
rs565248043 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102277445 | GTGTAGTGGCGTGGT[A/C]TTGGCTCACTGCAAC | 51366 |
rs565269138 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102405496 | GACAGAAACATGGAT[A/G]CTAACTAGAGTCTGT | 51366 |
rs565270922 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102253969 | TTTGCTGAAACAGTT[C/T]CCACAAAGGCAGCAG | 51366 |
rs565286452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102329543 | CTTTAGCACAGCCTA[C/T]AAGGTATCCAATTAA | 51366 |
rs565287212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102284804 | CACTTTGGGAGGCCA[A/G]GGTGGGCAGATCACA | 51366 |
rs565307217 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102406723 | TTTATTGATTTTTTT[C/G]TTTTTTTGTTTTTTG | 51366 |
rs565328839 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102366528 | ATGTTCCTGATCTTA[A/C]TCTCAAAAAAACTAA | 51366 |
rs565394475 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102296591 | CTCCGCTGCATAATA[C/T]ACTCAGGAACATTCT | 51366 |
rs565415630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102268307 | TCCTGACCTCGTGAT[C/T]CACCCGCTTTGGCCT | 51366 |
rs565429828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102264162 | TACCAATTTATAAAT[A/G]GGGAAACATGGCAGA | 51366 |
rs565454867 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102348629 | TCACTTCAGCTTTTT[A/C]AATTAGGGCAGTGTC | 51366 |
rs565456036 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102344056 | TCTGTTATTTTAAAA[C/T]TTTATTCCTAAGTAC | 51366 |
rs565476765 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102356486 | AATAATGGGCCGGGT[A/G]CAGTGGCTCAGGCCT | 51366 |
rs565482687 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102374591 | ATCCCTTCTGAATGG[A/C]ACTGTCAGAAAAAAG | 51366 |
rs565509042 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102328684 | CTCCACCTCCCAGGT[C/T]CAAGCAATTCTCCTG | 51366 |
rs565511607 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102398900 | AGGGATTAATAATGA[C/G]AATATCTAAGGAGCT | 51366 |
rs565518207 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102271753 | AGTTTCCTCATTCAC[A/C]TCTCCTAATTTCTTC | 51366 |
rs565544204 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102373935 | TGAGGGGCAGCTTGG[A/T]GAGGTGTGAAGAGTA | 51366 |
rs565554434 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102277898 | GCTACTTGGGAGACT[A/G]AGGCAGGAGAATCGC | 51366 |
rs565588813 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102354503 | TCATCTATTGTTCAA[C/T]GGTCACAAGTAACAG | 51366 |
rs565589057 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102385395 | AATTCCTGGTTATCT[C/G]AACTTCTCCAAATTA | 51366 |
rs565590608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102297936 | CTCATAAACTATTTA[C/T]CAGTGTTTTAAAAAG | 51366 |
rs565623689 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102260870 | AGTAGGACCCTAAAA[C/T]AGTCATTTTGGTACC | 51366 |
rs565640690 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102253222 | TCTTATAGTCCAGGT[A/G]TATATAAACTTCCAG | 51366 |
rs565661359 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102336628 | CTATCTTTTCCCCAC[G/T]GGTGCCCTTGTCAAA | 51366 |
rs565667371 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | UBR5 | GRCh38.p7 | 8:102348864 | TACATCAAATTTCCA[A/T]GGTTTCTCCTCTCAC | 51366 |
rs565678341 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102306727 | AGTAACAGCAAATTA[G/T]TTAGTTAGAAGCAGC | 51366 |
rs565683814 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102356015 | TCTATTATAATTGGT[A/T]ATTTCCAAGTTTTAA | 51366 |
rs565686317 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102311986 | CCACACTTGTAAGTC[A/T]ATTCAAACAGATACA | 51366 |
rs565691720 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102293407 | ATTAGAAACATTTAT[A/C]ATGGAGTTATTTTAG | 51366 |
rs565717636 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102261498 | ATGAGGTCAGGAGAT[A/C]GAGACCATCCTGGCC | 51366 |
rs565732286 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102312581 | TTAATGTTAAAGGAA[C/T]CCAATTCTTTGTATG | 51366 |
rs565767920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102318059 | AAAGGAACGCAGTTC[C/T]TCACCAGCAACGGAA | 51366 |
rs565789960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102289923 | ACAGCAAGTGTTTAA[C/T]AGAAGTGATCTAACT | 51366 |
rs565811262 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102331141 | AACATACAAAATATG[C/T]TGTTAATCAACTTTA | 51366 |
rs565818102 | snp | A/G | 6.66256e-05 | 0.00577134 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102314760 | GTATGGCATTGATGC[A/G]CTGCTGGCAATTGAG | 51366 |
rs565818776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102334534 | TGACCTCAAGTGATC[C/T]GTCTGCCTTGGCCTC | 51366 |
rs565861845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102340904 | AACCAAGGAATAATG[C/T]ACTAAAAGTCTATAC | 51366 |
rs565880058 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102341617 | TTTATCTGCTAGTGG[C/G]GCCCCAAAGTTCCCA | 51366 |
rs565889136 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102412579 | CTGGCTGCGGGCTAC[C/G]GGGACGGTCTGGTCC | 51366 |
rs565918837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102386499 | TCTCCTCCATCAAAC[C/T]CCATGCAAAAGGGAA | 51366 |
rs565929085 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102307413 | AAACCACTAGTGCAG[C/T]AGGTTACAAGCAAAG | 51366 |
rs565961642 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102393226 | AATGACTTATGGGAA[A/T]CTTCATTTATATTTA | 51366 |
rs565985691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102377402 | CTGTGCCTAAAATCA[C/T]ATCGTTAAAAAATGT | 51366 |
rs566010702 | snp | A/G | 0.000891183 | 0.0210902 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102257698 | ACGCTTGAACTGCAG[A/G]AGCTTCTCAGCATTT | 51366 |
rs566017163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102339674 | ATTACTATGGACACT[A/G]ACAACCATACTTAAT | 51366 |
rs566029978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102332697 | GATCTCTCAGGTGGT[A/G]TTGGTCATTTACCAC | 51366 |
rs566053054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102397570 | GCCAGGCATGGTGGC[A/G]GGCGCCTGTAATCCC | 51366 |
rs566055370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102385123 | AACTGTTAAATGAGA[C/T]GCGTAAAAAGGAATT | 51366 |
rs566155195 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102331644 | CCTTACCAGTTTTCA[G/T]TGATGGACATGACAT | 51366 |
rs566162146 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102413807 | TACCGAGTTTCTACT[A/G]TAAGACACTTTCAGA | 51366 |
rs566164509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102398072 | TACCTGACTTCAAAC[C/T]ATACTACAGAGCTAT | 51366 |
rs566189730 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102395705 | AAAGTTTTGATGAAA[-/C]ATCTCAAAACATTCT | 51366 |
rs566241822 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102370636 | AATTATTGATAACTA[C/T]AGTCACCATACTGTG | 51366 |
rs566254205 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBR5 | GRCh38.p7 | 8:102362374 | TACAATGTAAAGATA[C/T]AATCAAATGCAGAGA | 51366 |
rs566264318 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102337898 | AAATTGCAAAAATGA[A/C]TGAGAAGAGAAAATG | 51366 |
rs566266234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102330793 | GTATTAAGGTAATGC[A/G]AATCATGGTAAGGGA | 51366 |
rs566311174 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102402770 | AATACCTCATCGCCT[C/G]AATTCTGAACAGCAG | 51366 |
rs566321517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102354468 | GGTAGCTCAAATCAA[C/T]GAAAAGCAGCTTATA | 51366 |
rs566322916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102368561 | ACCTCCTGAGTAGGT[A/G]GGATTACAAGCACAT | 51366 |
rs566333603 | snp | G/T | 1.69674e-05 | 0.00291263 | intron-variant | UBR5 | GRCh38.p7 | 8:102361209 | CAAAGGGGGGTGGCT[G/T]AGAGATAAAAAAAGA | 51366 |
rs566335634 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102353902 | TGGGCATGGTGGTGC[A/G]TGCCTGTAGTCCCAG | 51366 |
rs566341278 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102391454 | TAAAGTGTGATAATG[A/G]TAAAGTGGCTATATA | 51366 |
rs566352427 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102325690 | AAAACTGAGTAAATC[A/G]AGTGTATTAGTAATT | 51366 |
rs566371079 | in-del | -/ACCA | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102257542 | CCCAAAATTAAAATG[-/ACCA]ACCATTACAAACTTA | 51366 |
rs566390944 | in-del | -/TCCCAGC | 0.00517822 | 0.0506191 | intron-variant | UBR5 | GRCh38.p7 | 8:102377454 | GGCTCACGCCTGTAA[-/TCCCAGC]ACTTTGGGAGGCTGA | 51366 |
rs566393846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102288885 | ATTACGAATATCTTG[A/G]CTGGGCGCGGTGGCT | 51366 |
rs566395857 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102410951 | AAATGCTCCACTTTG[C/T]GATCCTGTAAACATT | 51366 |
rs566397653 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102253146 | AAATGAAAAGGTGGC[C/G]AGGCCAGTGCCATTT | 51366 |
rs566398439 | snp | A/T | 1.6486e-05 | 0.00287102 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102360636 | TCTGTCTGGCTGTAC[A/T]GAAAAACCAATCCTG | 51366 |
rs566440581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102273697 | GCTGCAAAAACTGCG[A/G]TAACAACCATTAAAG | 51366 |
rs566468713 | snp | A/G | 1.74958e-05 | 0.00295764 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102286610 | GAAGGCAGGAACACT[A/G]CTTGCTCCTAAAATT | 51366 |
rs566480025 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102408072 | ATCACACCAAGCTGA[G/T]AAGTACTAATCTAGA | 51366 |
rs566487431 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102322741 | GTGGCACATATACAC[C/G]ATGGAATCCTATGCA | 51366 |
rs566529927 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102377138 | GAACATGGAACACTC[A/G]CTAGTAAGATCTTGG | 51366 |
rs566530467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102383073 | AATTTTGGAAGCTGG[A/G]AAGCCGACAGACAAG | 51366 |
rs566551559 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102287270 | CTGGAGAAAGAGTTA[A/T]TAAAATAATACTTTC | 51366 |
rs566593276 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102390380 | CAAAAATTAGCCTAG[C/T]GTGGTGGCAGGCACC | 51366 |
rs566593329 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102382001 | CAGATATTTCCATTT[A/C]ATAGTGAGTCTTTGG | 51366 |
rs566607983 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102409077 | AACGTAGTACTAACT[C/G]AAGAAATCCATTGGA | 51366 |
rs566622279 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102260027 | GCAAGACACTGTCTT[A/T]AAAAAAAAAATATTT | 51366 |
rs566645003 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102404602 | AAATGCTGTCATACC[A/G]GAGGTTAAGAAGTTA | 51366 |
rs566648974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102310896 | GATCCCTACCAGAAT[C/T]CTGGTCATATCAAAA | 51366 |
rs566655554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102317043 | TTCCATTTGAGGTAC[C/T]GGGTTCATCTCACTA | 51366 |
rs566695918 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102399645 | ATGTCTTCAAATCTA[C/T]GTTATCTTAAACAAT | 51366 |
rs566698285 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102266619 | GCGTGAGCCACCACA[C/T]CTGGTGAATTAGTCC | 51366 |
rs566719668 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102264361 | ATAATGGCTGTAATG[C/T]TTTAAGATTTAATAG | 51366 |
rs566736233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102310463 | GTGATTCTTGTGCCT[C/T]AGCCTCCTGAGTAGC | 51366 |
rs566754450 | in-del | -/CAGT | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102260870 | AGTAGGACCCTAAAA[-/CAGT]CATTTTGGTACCATA | 51366 |
rs566754842 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102411585 | TCACCTTCCCCCCAC[C/T]CCCCGCCCGCTCCCA | 51366 |
rs566771449 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102395089 | AACACCTTGTCCTAC[A/G]TCCTACATCCTACAG | 51366 |
rs566790523 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102264284 | AGTCTTTTTCTGTCA[A/T]TAATTTATTAATTTT | 51366 |
rs566817214 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102315731 | GGTGGGGGGAAGCCA[A/C]TACTGATTAATCACT | 51366 |
rs566849157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102352226 | AGGCAGGAGAATCAC[C/T]TGAACCCAGGAGGCA | 51366 |
rs566866407 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102309728 | TACCATCTAGGTTCA[G/T]GTAAGTGCACTATGT | 51366 |
rs566868823 | snp | C/T | 1.64827e-05 | 0.00287073 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102342618 | AGCCACCTTCGTTCA[C/T]GTAAACGTAAAACGG | 51366 |
rs566899334 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102321433 | ACTGCTCAAGGAAAT[A/T]AAAGAGGATACAAAC | 51366 |
rs566908970 | in-del | -/A | 0.00914312 | 0.0669923 | intron-variant | UBR5 | GRCh38.p7 | 8:102323963 | GTGAGACTCCATCTC[-/A]AAAAAAAAGAAAAAG | 51366 |
rs566924276 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102317377 | GCAAGGCGGCAGCCA[G/T]GCTGGGGGAGGGGCG | 51366 |
rs566957953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102394554 | TTTTCACCTCTTAGA[C/T]AGAAAAACACATTGT | 51366 |
rs567010638 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102370704 | TTTTGTACCCGTTAA[C/T]CAACCTGTCTTCATC | 51366 |
rs567016424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102394073 | GAAATTTATTCTTTT[C/T]CTTTTTCTTGAGACG | 51366 |
rs567116329 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102334147 | GCTTAAACAAGGGGT[A/C]AAATGAAATGGATCC | 51366 |
rs567126745 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102277690 | CAGCCTTACCCACCC[A/C]CCTCCTTTAAATTCA | 51366 |
rs567150020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102343781 | ACTTGAACCGGGAAG[A/G]CAGAGATTGCAGTGA | 51366 |
rs567158305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102351419 | TAAGCCTGTCACACA[C/T]ACACACACAAAAAAA | 51366 |
rs567164097 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102328823 | GGCTAGGCTGGTCTC[A/G]ACACCTGACCTCATG | 51366 |
rs567165827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102395638 | TAATCTAAGCACTCC[A/G]GCCCTCAGTTTCCTC | 51366 |
rs567166685 | snp | A/G | 1.67114e-05 | 0.00289057 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102299531 | AGCGGGGGCCAGGAT[A/G]AAATCAATGTCACCA | 51366 |
rs567184028 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102257838 | TTAAGACTTGGGGGG[A/G]AGCGTCTAATTCCTA | 51366 |
rs567196877 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102372787 | TGTTAAAATGTATAC[C/T]TACAACCAATTTCTT | 51366 |
rs567231608 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102386717 | GCGCGGTGGCTCATG[A/C]CTGTAATCCCAGCAC | 51366 |
rs567242613 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102388031 | CATGTGTAAAACACA[C/G]GCTCTTTTTCACATT | 51366 |
rs567248870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102284460 | TTCCTACGATATGAA[C/T]GGATTTTTAAAAACA | 51366 |
rs567251315 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102410010 | ATCTGCCACCTTGAT[A/G]CACATGTTATGACTC | 51366 |
rs567264312 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102342938 | GAGTGGAACTGCTTT[A/C]TTTTGAAGTATATTT | 51366 |
rs567267739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102335100 | AAAGGAGATCTTGCC[A/G]TTTGCCACAACATGG | 51366 |
rs567325863 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102350559 | ATCTTACATTATATA[C/T]AAAAATTAACAAAAA | 51366 |
rs567354687 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102376663 | CGCCCGCTACCACAC[C/T]TGGCTAATTTTTTTG | 51366 |
rs567362698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102400304 | AAAAAGAAAGGTAGA[A/G]AAACAATACATGGCA | 51366 |
rs567410231 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102307770 | TCACTTGACACAGTT[A/G]GTCCCAACATCCTGC | 51366 |
rs567415246 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102394922 | ATTAACAAGGTATCC[-/T]TTTCTACAAGAACAT | 51366 |
rs567415649 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102320741 | AAAAAGCTTATCCAC[A/C]ATGATCAAGTGGGCT | 51366 |
rs567417296 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102388712 | ATAGTAAAGAACTAA[C/T]CGCTAGCTCACATTT | 51366 |
rs567417820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102271347 | AAATGTAAGAAAACA[C/T]GACAGCTAAAGATTA | 51366 |
rs567453542 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102341552 | CGCCTTCAATATCCC[A/G]GATTCAAGTTCTAAA | 51366 |
rs567479061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102292193 | CCAGAGAATGGTCAA[A/G]GTCTGTGTTTTTCAA | 51366 |
rs567495287 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102373336 | TTCATTTGTTTAACA[C/G]TAAGACTATATATAC | 51366 |
rs567504384 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102357355 | GCTGCTTAGGGAACA[C/T]AGTGAGAGACCCTGT | 51366 |
rs567554281 | snp | G/T | 1.68647e-05 | 0.0029038 | intron-variant | UBR5 | GRCh38.p7 | 8:102275855 | TTAAGGGAAGGGGTG[G/T]GGGGGAGAAATAATT | 51366 |
rs567564745 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102364540 | AATGGAAGATATATA[C/T]GTAATGTTTACAATG | 51366 |
rs567566528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102356714 | GCAGTGAGCCGAGAT[C/T]GCGCCACTGCACTCC | 51366 |
rs567574210 | snp | C/T | 1.66663e-05 | 0.00288667 | intron-variant | UBR5 | GRCh38.p7 | 8:102326510 | GATTCTGAAGAGAAA[C/T]GAGGTCCCTTAAGAC | 51366 |
rs567578165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102364136 | GGAAGAACTCTTTTA[A/G]TCATCTCCGGTTCTG | 51366 |
rs567608956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102327219 | CATATTTTCTTCCAA[A/G]TAATTATACTTCATT | 51366 |
rs567611957 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102378178 | CTATCATTGTGTTTT[C/G]TCACTATGGAGCACA | 51366 |
rs567655972 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102324794 | TACAGATGCAGCTGA[A/G]TAAGTGACCAACAGT | 51366 |
rs567674039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102283263 | AAAAGACCACATACT[A/G]TATGATTCCATTTAC | 51366 |
rs567682318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102378724 | AATAACTCAATGTAC[A/G]CTGACTCAACAGACT | 51366 |
rs567705494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102262821 | AAATCCTCAAAGCCA[C/T]TGGCTGGATGTGGTG | 51366 |
rs567716497 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102379400 | AAACAGAAAACAAAC[C/G]TAACAAAATGGAGGC | 51366 |
rs567775112 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102289833 | CCATCCCATCGAAAA[A/C]TTCTACAGGAAGATT | 51366 |
rs567798170 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102275966 | TCTTCAAACTGTGTC[C/T]TAACAGAGAACTTTT | 51366 |
rs567801053 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102412440 | GAGGGCGAATCCACA[C/G]GCCACCCGCTCCCCC | 51366 |
rs567820684 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102372065 | AGCTTAGCAACTATA[C/G]GCCTCCGGGTTTGAC | 51366 |
rs567822079 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBR5 | GRCh38.p7 | 8:102407539 | GTAGGCTGAGGCAGA[C/T]GGATCACCTGAGGTT | 51366 |
rs567839609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102314063 | TACTGCTTTATGAAT[C/T]GGAGTTTTCTGATCA | 51366 |
rs567839743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102306836 | ACTTAGTTGTGTTAC[A/G]AGCAGAAAAGTTTAC | 51366 |
rs567846546 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102273099 | GTTAAAAAAAAAATA[C/T]TAGAAAAAAAACAGA | 51366 |
rs567847200 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102319201 | AAACCCATCTCACAT[C/G]CAGAGACACACACAG | 51366 |
rs567887323 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102262207 | TTTCCCACTGGGTAT[A/C]TAACTATTTAAAGAG | 51366 |
rs567913582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102340722 | GGCTTAAGCTGTTTT[C/T]TTTCCCAGAATTCAA | 51366 |
rs567926514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102313208 | GCTGCAGAAACTGGT[A/G]TATCTGCTCTTTCCT | 51366 |
rs567935957 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102269189 | TCTTTTATTTAAAAA[A/T]AAAATAAAATAAGAA | 51366 |
rs567937019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102405559 | AGCGCAGTGGCTCCC[A/G]CCTGTAATCCCAACA | 51366 |
rs567968315 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102306154 | TATCATTAGCTTTCT[A/G]ACAAATAGCATGAAT | 51366 |
rs567971800 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | UBR5 | GRCh38.p7 | 8:102346581 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAA | 51366 |
rs567995504 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102318752 | TCTCTCGGCAGAAAC[C/T]CTACAAGCCAGAAGA | 51366 |
rs568008298 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102414390 | GATAATGGAACACTT[C/T]TGTAGGTTACCAGCT | 51366 |
rs568030822 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102366675 | GTAACTCAATAATCA[C/T]ATTAGGAAACTGCCT | 51366 |
rs568041818 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102341576 | TTCTAAATCAAAGAA[A/G]GAAAAGAAATCCATA | 51366 |
rs568046097 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102362883 | TTTTTTTTGAGTCTC[C/G]ATCTGTTGCCCCAGC | 51366 |
rs568055391 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102312549 | ATCAACATACAAATT[A/C]TATTCACTGAACTAA | 51366 |
rs568096312 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102267613 | AAACGAACAGTACAT[A/T]AAATCCAGAGAAGAA | 51366 |
rs568107060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102362263 | TTGTATTTTCTGTTA[C/T]GATTTTGTTGTTTCT | 51366 |
rs568115013 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102317587 | CTTTGAAGAGAGCAG[C/T]AGTTCTCCCAGCGTG | 51366 |
rs568115891 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102262701 | TGTACTAATAGAAAA[G/T]TATTCATCAGTAGGT | 51366 |
rs568132620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102274663 | CCTGAACCCAGGAGG[C/T]GGAGGTTGCAGTGAG | 51366 |
rs568154645 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102306827 | ATCAATACTACTTAG[C/T]TGTGTTACAAGCAGA | 51366 |
rs568156748 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102366309 | ATGAACCTTTCCTGG[C/T]AGTTGTAATTTCCTT | 51366 |
rs568165869 | in-del | -/T | 0.00636936 | 0.0560724 | intron-variant | UBR5 | GRCh38.p7 | 8:102325642 | AACCTTATGTTTATA[-/T]GGGTCATATCTAGTT | 51366 |
rs568167753 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102377255 | ATCTAGAACATAGAA[A/T]CCTCCTCCAAAAGGC | 51366 |
rs568180343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102369235 | GTTACGGAAAAGTGA[A/G]GTACATTTTAATATC | 51366 |
rs568212660 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102292386 | ACAAGCAAAGGGAAT[A/G]GAATAAAGAGAGTTT | 51366 |
rs568218295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102296792 | AAGTAACCTCATGCT[C/T]TCTGAAGTAAAACAT | 51366 |
rs568231254 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102309168 | GGTTCAAGCGATTCT[C/T]GTGCCTGAGCCTCTT | 51366 |
rs568234869 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102355885 | AAAATTAGCCCTAAT[C/G]TTCTTCAGAGTAGGT | 51366 |
rs568238553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102347954 | ACATTGGTCAGGCAT[A/G]GTGGCTCATGCCTTG | 51366 |
rs568262375 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102297313 | ACTGAGCAATCAGCT[A/C]TTTTGCCTCATTTAC | 51366 |
rs568288819 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102281974 | AAGAAAACACAGATA[G/T]CCTGGGCAACATGGT | 51366 |
rs568294475 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102392538 | AAGCCTCCTAAAGAA[A/C]ATACAGGAAAAAAAA | 51366 |
rs568315063 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | UBR5 | GRCh38.p7 | 8:102321446 | ATAAAAGAGGATACA[A/C]ACAAATGGAAGAACA | 51366 |
rs568315826 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102283232 | ATCATTATGCTAAAT[G/T]AAAGAACCCAGTCAC | 51366 |
rs568324458 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102273978 | CTGTAGATATTTTAC[A/G]TTGATTACAAAATAA | 51366 |
rs568326322 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102281196 | GTTCTCTTTTGCAAT[A/G]CTATTCTCCTTACTC | 51366 |
rs568353677 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102406065 | CGTATTCCTGTGTAT[A/C]CTGTAATTTTCTTCA | 51366 |
rs568377813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102261440 | AGGCGCAGTGGCTCA[C/T]GCCTGTAATCCCAAC | 51366 |
rs568400801 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102256063 | AAAACGGCAGAATTG[G/T]GAGGCCAAGACAGGC | 51366 |
rs568420383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303662 | TACACATCACCCTTT[C/T]ATTTTTTTCCCAGAT | 51366 |
rs568453834 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102354406 | CAAGTAAAATTATAC[A/C]TTTCAATTCACGTAC | 51366 |
rs568456664 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102391430 | TAGGGAATTTTTGTT[A/G]ATTTCCTATAAAGTG | 51366 |
rs568460222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102338080 | GGAAAGGTGGATGGA[C/T]GGAAGGATGGAAAGA | 51366 |
rs568462013 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102304564 | ACCTGCAAACCACTA[C/T]TCAAAAATGTAGCTA | 51366 |
rs568462722 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | UBR5 | GRCh38.p7 | 8:102288892 | ATATCTTGGCTGGGC[A/G]CGGTGGCTCACACCT | 51366 |
rs568514036 | in-del | -/A | 0.0505692 | 0.150756 | intron-variant | UBR5 | GRCh38.p7 | 8:102256139 | AACCCTGTCTCTACT[-/A]AAAAATACAAAAAAT | 51366 |
rs568519923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102324728 | ATAGTTGTGTATCAT[C/T]AACTATAACTCCGTG | 51366 |
rs568536284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102274335 | GATGTAATTCTAAGA[C/T]TGCTACTGTGTATGT | 51366 |
rs568555684 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102281670 | AACCACTGTGCATGA[C/T]TTACAGCCTTATACT | 51366 |
rs568593219 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102376307 | ACATATTCTTAGGCC[C/T]CATTTAAACCTACTA | 51366 |
rs568645052 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102336491 | TCTCATAGTTTTTAA[G/T]GTTTCATATTTCACA | 51366 |
rs568665042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102258050 | TGGGTGGGGAATGCA[A/G]AGAGGGGAGACCAGA | 51366 |
rs568668063 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102384710 | TAAAAACCAAAAGAG[C/T]TCTGCTGAGCTGCAA | 51366 |
rs568669561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102265747 | AATGTATCTGGACAT[A/G]GTTTTCTTTCAGTTT | 51366 |
rs568717410 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102330615 | AAACTGCATCAAATT[C/T]TACCTTTCTACTTCA | 51366 |
rs568769957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102367276 | TGACACTTCTTAAAC[A/G]CTGCTTCTCATGCCA | 51366 |
rs568788077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102381959 | CAATATTTCTTAACT[C/T]TTTTGATCTCAGGAA | 51366 |
rs568846777 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102278648 | TGGATGAAGTGATCT[A/G]ACAGCAAGTTAATGA | 51366 |
rs568850347 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102380287 | TAGTCCCAGCTACTC[A/G]GGAGATTGACACAGG | 51366 |
rs568852055 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102405963 | CAATTAAATTTTCCT[C/T]TGGAAACTATTTCCT | 51366 |
rs568854731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102329890 | GCGTACAAGTAGGTG[C/T]TCAATCAATGTGCTG | 51366 |
rs568880641 | snp | A/G/T | 3.29485e-05 | 0.00405874 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102286481 | ATGGGAGCTATTTGT[A/G/T]GTTCTTTCTAATGGC | 51366 |
rs568894556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102315035 | ATAAAAGGTACACAA[C/T]GCATGCTTTCAAATA | 51366 |
rs568925390 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102381202 | GAAACCCCGTTTCTA[C/T]GAAAAATACAAAAAT | 51366 |
rs568990379 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | UBR5 | GRCh38.p7 | 8:102320508 | CCAAATTCTACCAGA[C/G]GTACAAGGAGGAACT | 51366 |
rs569054492 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102317005 | CCAGCGTCAGCTACT[C/G]AGAAGACAGGTGATT | 51366 |
rs569078600 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102359999 | TGAAGATGATCATTC[A/T]GACTGAGAGCACTCA | 51366 |
rs569080955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102273634 | TCACACTATCTGTAA[C/T]AGCAAAAGACTGGAA | 51366 |
rs569092937 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102375382 | ATAAAAATAAAATGA[A/T]TAAAAAATAAAAGTG | 51366 |
rs569101598 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102322653 | CACGTATGTTTACTG[A/C]GGCACTATTGACAAT | 51366 |
rs569102233 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102319968 | AATTTAGAACACTAA[A/T]TGCCCACAAGAGAAA | 51366 |
rs569147379 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant | UBR5 | GRCh38.p7 | 8:102299130 | AAGGAGCAGTTACAA[-/T]TTTTTTTTAAAAGAA | 51366 |
rs569221463 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102410405 | GTTCTGTTAATGACC[A/G]TAGAGCTATCCTCAC | 51366 |
rs569222450 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102358258 | GACTTTTACTGTAAA[A/G]GGCCAAATCATAAAT | 51366 |
rs569267316 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102380140 | GGCTCAGGCCTGTAA[A/T]CCCAGCACTTTGGGA | 51366 |
rs569278918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102400243 | GTTGCTTGAGCCCAG[A/G]AGTTCAAGATCAGCC | 51366 |
rs569295627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102328674 | TCACTGCAACCTCCA[C/T]CTCCCAGGTTCAAGC | 51366 |
rs569318751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102270400 | AAGGGAGTAGGACCT[C/T]AACATACCAGATATC | 51366 |
rs569365389 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102392177 | GTTGGCCTGTCAGGT[A/G]TATTATTTACTAGGG | 51366 |
rs569407538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102309091 | AGAGTCTCACTCTGT[C/T]GCCCAGGCTGGAGTG | 51366 |
rs569423795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102359068 | AAGCCACCACACCCA[A/G]GCCCAATTTTCAAAT | 51366 |
rs569482818 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102284842 | GAGATCAAGACCACC[A/C]TGGCTAACACAGTGA | 51366 |
rs569488737 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102409060 | ACAATGTTTTAAGCA[A/G]GAACGTAGTACTAAC | 51366 |
rs569501760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102257046 | AAGTCTGCAGCATAC[C/T]GCCTTTCAAGATTAA | 51366 |
rs569507115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102351558 | ATTTAACGGGTATAA[A/G]GTTCCAACTTCACAA | 51366 |
rs569522566 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102284268 | AAAAGAAATGTGATT[A/T]GAGAAAAAAAGAGCA | 51366 |
rs569537512 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102371458 | CAAGTCATAGTTCCT[C/T]AAAAATTAGTTACAA | 51366 |
rs569570800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102307558 | TAATGGAGGGTGAAT[A/G]TGCTCCCATATTAAA | 51366 |
rs569603361 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102255275 | CTCTTAAGGAAAAGC[C/T]TTTTTTTTAATCTAA | 51366 |
rs569609001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102291327 | GGTGATAAAGAGAAA[C/T]GACTGTACTGTATAA | 51366 |
rs569619406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102394012 | TTCAATGATTTTCAC[A/G]TTCTTATTTTAGGTG | 51366 |
rs569646456 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102360341 | AAACACGTAATATCA[C/T]TCTTCTGGTAACCTG | 51366 |
rs569678721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102349654 | CCACTTAACAGTAGC[A/G]TCAAAAAAAAACAAA | 51366 |
rs569690365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102306807 | TGGGCTCTCACACTG[A/G]GAGTATCAATACTAC | 51366 |
rs569691750 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102277401 | TTTTTTTTTTTTAGA[A/C]GGAGTCTTGCTCTGT | 51366 |
rs569704358 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102356657 | CCCAGCTACTCGAGA[G/T]GCTGAGGCAGGAGAA | 51366 |
rs569705383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102335588 | GAGTCTTGCTCTGTC[A/G]CCCAGGCTGTAGTGC | 51366 |
rs569712211 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102291385 | ATCCCAAAGGGACCC[A/C]CTGATGTCTCTTGGG | 51366 |
rs569777401 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102387824 | GAAAATCTAAAAACT[A/C]ATTCTACTTAATTTG | 51366 |
rs569787910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102328023 | TTTTGAGTTAAATGC[C/T]ATAAAAATAAGTAAT | 51366 |
rs569802457 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102277058 | TGCAGCAAGATCATG[A/G]GCAGATGGCCCTGGT | 51366 |
rs569853810 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102336296 | CATGGTTTGCAAATA[-/T]TTTTTCACAGTCTAT | 51366 |
rs569859709 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102379482 | TAAGTGTCAATTCAC[A/T]CTTGGACCATACAGT | 51366 |
rs569870998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102261581 | TGGCGCGTACCTGTA[A/G]TCCCAGCTACTGGGG | 51366 |
rs569884332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102298772 | TATTGTCCATATAGT[A/G]TAAGAAGATAAACTT | 51366 |
rs569918701 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102401261 | AAATTGACCAAAGGA[A/T]GACAAAGACTGAATC | 51366 |
rs569922051 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102386968 | TGACAGAGCAAGACT[C/G]CGTCTCAAAAAAAAA | 51366 |
rs569957466 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102282138 | CACGCCACTGCACTC[C/T]GGCCTGGGCAACAGA | 51366 |
rs569960494 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102268394 | TTTTTAGTAGAGATA[C/T]GGTTTCACCATGTTG | 51366 |
rs569964533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102371433 | TCTCTGATACTACAT[C/T]AAAACTCAACAAGTC | 51366 |
rs569968052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102333215 | AGATTTATCTGTATT[A/G]AAGAAATTTACTGTA | 51366 |
rs569999193 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102342825 | GCTGACATGCAACAT[A/T]CAAAACATCAACCCT | 51366 |
rs570042194 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102385241 | TCTATCATTACACCC[C/G]AATAAAAAATAAGCA | 51366 |
rs570052704 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102356678 | GGCAGGAGAATGGCA[C/T]GAACCCAGGAGGCGG | 51366 |
rs570057919 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303696 | GATATCTGAGAAACT[C/G]ACCTAAATAAGCAAT | 51366 |
rs570058601 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102356317 | TAGTCAAGCGTGGTG[C/G]TGGGCGCCTGTAATT | 51366 |
rs570133581 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102312639 | ATCAACCCAGACAGA[C/T]TCTGAGCTTTGCTAC | 51366 |
rs570147643 | in-del | -/AATT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102314425 | GACCAAGACATAATC[-/AATT]TACAATAATAAGAGT | 51366 |
rs570191925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102324397 | TTTAGGAGTAAATAA[C/T]TTACAGAGAAAAAAA | 51366 |
rs570193659 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime | UBR5 | GRCh38.p7 | 8:102252746 | CATTCAGTTTTAAAT[A/G]TTTTTAGTGTTAACA | 51366 |
rs570217891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102363920 | TAGCACAAATGGTTA[C/T]TGCTATCAATTAAAT | 51366 |
rs570232362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102327136 | AACTCCCAGGCTCAA[A/G]CAATCCTCTGGCCTT | 51366 |
rs570247599 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102318660 | ACCAAAGTTGAAATG[A/T]AGGAAAAAATGTTAA | 51366 |
rs570253497 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102323289 | GGTGTCAAAGCACGA[G/T]TAGTTAAGCTATAGT | 51366 |
rs570264726 | in-del | -/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102405096 | GTCAATCAGAAATAA[-/G]CATTTATGAGACAAC | 51366 |
rs570334424 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102318207 | AAAAATTTAGACGAA[C/T]GTATAACTAGAATAA | 51366 |
rs570338749 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102361459 | AAAAAGTTGACAGAT[G/T]AAAAGATTCTTAAAG | 51366 |
rs570370840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102326401 | CAGTATTACTCTACT[A/G]AATGAAGGAAGAATG | 51366 |
rs570379796 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102276602 | AATTCTCCCCTGTCT[C/T]ACATCGTTATTAGAC | 51366 |
rs570418703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102266823 | GCTTCTGTCTCTCTA[C/T]TGTAAACATTCATTT | 51366 |
rs570460095 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102317540 | AAAAGACAGCAGTAA[A/C]CTCTGCAGACTTAAA | 51366 |
rs570466116 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102259298 | TTCTTAGGATTCAAA[A/G]GAGAGAAAGGCAGGA | 51366 |
rs570511960 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102369189 | TTTGGTATATGAAGT[A/G]TATGAAGAAAAGCTG | 51366 |
rs570524432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102376042 | GAAAAGGCAAAATTA[A/G]TGCCAGACTGGTCCT | 51366 |
rs570567181 | in-del | -/AAAC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102285040 | GACTCCGTCTCAAAA[-/AAAC]AAACAAACAAACAAA | 51366 |
rs570568499 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102332462 | ATATCCTAACTTCTT[C/G]CTTGGCAAACTGTCT | 51366 |
rs570585700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102375518 | TCAAATGGTGCTATA[A/G]GAGTATGAGGAATTT | 51366 |
rs570588518 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102402625 | AACAAGGAGGCTGTC[A/C]CGGAAAACACCCAAA | 51366 |
rs570590954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102265005 | TGTGAGCCACCGCAC[C/T]CAGCGTACATACATT | 51366 |
rs570616696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102304766 | TCTAAAAATTTAGAT[A/G]AAAGTTGCCTCAATG | 51366 |
rs570629803 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102256176 | GGCGTGGTGGCAGGC[A/G]CCTGTAGTCCCAGCC | 51366 |
rs570634253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102379102 | ACATCTCAAAGCATA[A/G]CAAGTTTATTGGTAT | 51366 |
rs570649138 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102305451 | AAAGAAACAGAACTT[A/C]AGGGTACACTTTAAG | 51366 |
rs570653744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102409931 | CAAGACATGTTTACC[A/G]CTACTAGATACAACC | 51366 |
rs570690066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102362141 | GATCATCAATGTCCT[C/T]ATCTATATAAAGTAA | 51366 |
rs570697739 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102370453 | TTTTAACTGATAGAT[A/G]TATTTATGGGGTGCA | 51366 |
rs570740767 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102405527 | TTTCTTAATTAGAAA[G/T]ATGTATAATATGGGC | 51366 |
rs570740868 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102267534 | ATGTACATTGTTCTT[C/G]ATTTTTCTATAATGG | 51366 |
rs570764196 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102352403 | TCAGGAAAAACTATC[G/T]TCAGTCATTTTTAAA | 51366 |
rs570767113 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102412259 | CTTCTCGTCCTCCAC[G/T]CGAGGGCGGCCCCCT | 51366 |
rs570775953 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102264827 | CATCCTCCTACGCCA[C/G]CCTCCCAAGTAGCTG | 51366 |
rs570802625 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102257966 | AAAACTGATATTCAC[A/C]TGAGTTTTATCTCAT | 51366 |
rs570807493 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102294839 | CGATGCAATGCCACC[C/G]CATCCCTATCTGAGT | 51366 |
rs570809367 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102401932 | TTAAGAGAATGAATG[C/T]TTAGCCAGGCATGGT | 51366 |
rs570813305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102396981 | TAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACCA | 51366 |
rs570817063 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102309788 | CAATGTATTTCTCAG[A/C]ATGTATCCCTGTCAT | 51366 |
rs570823064 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102359937 | CAATATGAACTTCCT[A/G]CCCAGAGTTCAGGAG | 51366 |
rs570826187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102360376 | TGTTAAGTGATAACT[A/G]ACTCCTCTGCTACTT | 51366 |
rs570857531 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102367336 | AATTCAAACTATCAC[A/G]TGGGGTGGTCCCACC | 51366 |
rs570861050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102353079 | CCACCTACCAGTCCC[C/T]GTACGTCAATCGCCA | 51366 |
rs570904847 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102316379 | CATTGATGTGTTAAA[A/T]GTTCTTTCTAGAATG | 51366 |
rs570910950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102331743 | GATTTGCCTCTGTTC[A/G]TTATCTGTTCTGGAA | 51366 |
rs570935389 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102380361 | ATCGTGCAACTCCAG[C/T]CTGGGCAACAAAGCT | 51366 |
rs570964436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102287364 | ACACAAAGTATGACC[C/T]AATCCACGCTGAATA | 51366 |
rs570980922 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102338572 | TCCCATGACCTGCAG[C/G]AACTGCCCGTTCTCC | 51366 |
rs571041781 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102352117 | GTTCGGGACCAGCCT[A/G]GCCTACCTGGTGAAA | 51366 |
rs571045382 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102390469 | GCAACAGCGAGACTC[G/T]GTCTCAAAAAAAAAA | 51366 |
rs571078005 | snp | A/G | 4.40752e-05 | 0.00469422 | synonymous-codon, nc-transcript-variant, intron-variant | UBR5 | GRCh38.p7 | 8:102264512 | TTACATGTCTATTCA[A/G]TGTGATAGGACATAG | 51366 |
rs571078008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102272869 | AATCTAGTTTTAGCC[C/T]TTCCTTGAGAGTTTA | 51366 |
rs571082799 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102383262 | AGGAAATTAGCATAA[C/G]GAAATTAGCATTAGT | 51366 |
rs571115275 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102272236 | GAAATGCTGCAATTT[C/G]ATCGGTGAATTTTTA | 51366 |
rs571146295 | in-del | -/ACAA | 0.00589593 | 0.0539741 | intron-variant | UBR5 | GRCh38.p7 | 8:102324093 | TCCATTCTGCTACAA[-/ACAA]ACAAACAAACAAACA | 51366 |
rs571147841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102374929 | CCAATACCTGACACA[C/T]AGTAAATGCTTATTT | 51366 |
rs571168486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102344643 | TTTTGAAAATAGCAT[C/T]TTAGGCTGGGCGCAG | 51366 |
rs571190892 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102388708 | AGTCATAGTAAAGAA[C/T]TAATCGCTAGCTCAC | 51366 |
rs571191891 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102346145 | ACCACCTTGAAAAGA[A/G]TATTCAGAAAAGTCT | 51366 |
rs571193175 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102381749 | GAACAAATATAATTT[C/T]ACCAACTTTTCATTT | 51366 |
rs571216155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102328822 | TGGCTAGGCTGGTCT[C/T]GACACCTGACCTCAT | 51366 |
rs571230160 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102284954 | GGGCAGGAGAATGGC[A/G]TGAACCCAGGAGGCG | 51366 |
rs571238380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102335768 | TGGCCAGATTGGTCT[C/T]GAACTCCTGACCTCA | 51366 |
rs571242394 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102406355 | CTGGAGTGCAGTGGC[A/G]CAATCTTGGCTCACT | 51366 |
rs571253409 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBR5 | GRCh38.p7 | 8:102395384 | TTAATGATTTCACAT[A/G]TATCTATTTATATAT | 51366 |
rs571271196 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102319276 | AACAAAAAAAGGCAG[A/G]GATTGCAATCCTAGT | 51366 |
rs571321043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102394727 | AGAGAGGTGAAGTAC[A/G]TTCTTTGTAGCCACA | 51366 |
rs571330062 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102367053 | CTTGGAGTGGTGGTC[C/T]TGCCTATACCATTTT | 51366 |
rs571350893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102343878 | GGGGGGGTGGGCAGG[A/G]GGGAGAACATGGGAA | 51366 |
rs571362692 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102292370 | GAAGTTGTCTCAAGA[A/C]ACAAGCAAAGGGAAT | 51366 |
rs571384273 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBR5 | GRCh38.p7 | 8:102318941 | GCTCCTGAAGGAAGC[A/G]CTAAACATGGAAAGG | 51366 |
rs571393884 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102369314 | AGCAAGTGATTTCTT[-/A]AAGGTTGAGAGCAAT | 51366 |
rs571400889 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102299618 | ATGTTCTCTTAACTG[G/T]CCTTAAGGCTTTTCT | 51366 |
rs571405170 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | UBR5 | GRCh38.p7 | 8:102315864 | TGCTAATATTTGAAA[C/T]GGCTGATTTCAAGGA | 51366 |
rs571411898 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102407702 | GACGTTGCATTGAGC[C/T]GAGATCCGGCCACTG | 51366 |
rs571423133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102279507 | TGTGCCATTTTGTAT[C/T]GGACAAAGGTTTCCC | 51366 |
rs571446765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102327285 | TTTTGCTGTTAACTC[C/T]TTAAAACACAACAAA | 51366 |
rs571457961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102366083 | CCTTCAAAGGTTTCA[A/G]TTCTCAAAGACAGAA | 51366 |
rs571478211 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102384066 | ATAAATTTGCTTTCA[C/T]CTTAATAAACCAAAA | 51366 |
rs571479052 | snp | C/T | 1.65291e-05 | 0.00287476 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285623 | CCGAGATTTGTCTAA[C/T]GACAATGCTGTAAGC | 51366 |
rs571499148 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102386282 | TAAAAACACAAAAAT[C/T]AGCTGGGTGTGGTGA | 51366 |
rs571508043 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102350676 | GATGCCAAAAAAACA[A/C]AGGCAACAAAAGCAA | 51366 |
rs571542973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102330471 | GTACCAGTCAAACCT[A/G]TTTTCCTATTTTCAA | 51366 |
rs571570542 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102357488 | AGGATTGCATTAAGT[A/C]CAGGAGTTCAAGGTT | 51366 |
rs571594343 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102364647 | GCTTCCCCAAATATC[A/C]AATTTTAAAAAACTC | 51366 |
rs571601202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102371604 | TTTTTTTTTTGAGAC[A/G]GAGTCACGGAGTCTC | 51366 |
rs571607968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102329868 | ACCACTGTAACTTAA[A/G]AACTTAGCGTACAAG | 51366 |
rs571608636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102320233 | GAAGAATCAAATAGA[C/T]GCAATAAAAAATGAT | 51366 |
rs571618450 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102407108 | ATCAATCTTAATTAA[-/T]TTTTTTTTTCCTTTT | 51366 |
rs571670028 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102412489 | GAGGCAGGCGGCCGG[A/G]ACCAGGGGCGCGCCG | 51366 |
rs571673980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102269562 | TATAAAATGTGTACA[C/T]ACAGTTATGCATAAA | 51366 |
rs571676490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102291207 | AGTTTTGGGGACTTC[C/T]AGTTCCAGCAATTTG | 51366 |
rs571685671 | snp | A/C | 0.00129022 | 0.0253663 | intron-variant | UBR5 | GRCh38.p7 | 8:102296848 | AGCAATATAAATCTA[A/C]ACAGCTTATAATATT | 51366 |
rs571789705 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102339132 | TAATTTTGGGAAATA[C/T]GTGTATTTTACAGTC | 51366 |
rs571792003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102386903 | ACTGCTTGAACCCAG[A/G]AGGCGAAGTTTGCAG | 51366 |
rs571792240 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102378824 | ACTAATATTACTGAC[A/C]AAGTAACATCTCACC | 51366 |
rs571816736 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102376564 | GGCTGGAGTGCAGTG[G/T]TGCAATCTCAGCTCA | 51366 |
rs571834939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102401019 | GGTCTTCAAGTTTTG[C/T]TGCTCCTGATGACGG | 51366 |
rs571849036 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102405647 | AACACGGTGAAACCC[A/C]ATCTCTACTAAAAAT | 51366 |
rs571856213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102255592 | GGGTAGATGACCTCA[C/T]TGCTGGATCTCTAAG | 51366 |
rs571861064 | snp | C/T | 0.000546398 | 0.0165197 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102326636 | TTTCTCTAACATTTT[C/T]TTCCTTTGACTAAAA | 51366 |
rs571892816 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102263097 | ATCTCAAAAAAAAAA[A/T]AAATTAATTAATTAA | 51366 |
rs571919306 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102323794 | GATGGTGAAACCTCC[A/G]TCTCTATTAAAAATA | 51366 |
rs571932301 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102308335 | TTAACCCTCTTGCTT[C/T]GTCTATTTGATACCC | 51366 |
rs571946976 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102400351 | CTCCCTGAGCTCGCT[A/C]ATCTATAACCTCACT | 51366 |
rs571948819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102408275 | TCAACTGTTCCTCCC[C/T]GACCTTGAGGAGAGT | 51366 |
rs571956159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102314173 | GTACAAAGAAATAGC[A/G]TAAAATGTATTTTGT | 51366 |
rs572013478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102347630 | AAACATCACACTTTT[A/G]GATCCTTAAAAAAAC | 51366 |
rs572013926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102348061 | GAAACCCTGTCTCTA[C/T]TAAAAATACAAAAAT | 51366 |
rs572018981 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102254736 | GAGTTAGTAGAGGAA[A/C]AAAAGGTGACTTTCT | 51366 |
rs572022170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102391401 | ATGAATATACACTGA[A/G]TATTGGATGATATTA | 51366 |
rs572035400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102333495 | GGTCATAAATTTAAC[C/T]AGAAATCCTTCCTCA | 51366 |
rs572044080 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102280864 | TAAGAAATTAGCCAG[A/G]CATGGTAGCACACGC | 51366 |
rs572084986 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102397928 | ACATTCAATGCAATC[G/T]CTATCAAAACACCAA | 51366 |
rs572130836 | in-del | -/GGTT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102361263 | GTAAATACATCATAG[-/GGTT]TACTCTTAAATACAA | 51366 |
rs572134896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102355511 | CATTTACTATAAAGG[A/G]AAATATGTGTGACTG | 51366 |
rs572161213 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102279970 | CTGGAGTTGGGATAT[G/T]TTCTCTTTTCATTGT | 51366 |
rs572216801 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102334493 | GACGAGGTTTCACCA[C/T]GTTGGCCAGACTGGT | 51366 |
rs572218400 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102382390 | GAAGCCTAAACTTCA[A/G]GAAAAAAGGAAAGCT | 51366 |
rs572220211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102390744 | TAAGCCACTGCTAGT[C/T]ATAGGATGTTAATCT | 51366 |
rs572257787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102404839 | TTGAACCCGGGAGGC[A/G]GAAGTTGCAGTGAGC | 51366 |
rs572286863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102275073 | GAAAGTTTATCAAAA[A/G]TTATTGGGGCCATGT | 51366 |
rs572316271 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102317307 | CTCACCTGGCTCAGA[-/G]GGTCCTACGCTCAGA | 51366 |
rs572318204 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102284733 | ACCCATCACAAAGTC[-/A]AAAAAAAAAATGTAA | 51366 |
rs572321456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102411992 | CCGCGGCCCCCTGCC[C/T]CCGGGATGAGAAGTT | 51366 |
rs572346310 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102280662 | AAAATGGACTCAACA[A/G]AAGAAAAAGCAAATC | 51366 |
rs572381528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102385344 | TTCTGTATTTCATAC[C/T]TACTGTAAAAATAAT | 51366 |
rs572396308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102274373 | TTAAAACAAATGAGT[A/G]ATTTGATTAATGTTG | 51366 |
rs572423339 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303996 | ATACTGCTTTCTGTA[C/T]TTGGTTTTTTCCTCC | 51366 |
rs572435298 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102411432 | TTTCAGGAGGAGAGT[A/G]AAGGGAATCCAATGC | 51366 |
rs572457485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102287782 | AATTATGGTAGTCAA[C/T]AGACTAGTACATCAG | 51366 |
rs572475609 | in-del | -/T | 0.171057 | 0.237209 | intron-variant | UBR5 | GRCh38.p7 | 8:102344491 | CTAATTGTTTTTGTA[-/T]TTTTTTTTTTTTTAG | 51366 |
rs572485949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102331884 | ACCATGCACTCCCTG[C/T]CACTGATTCTGTGTT | 51366 |
rs572546987 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102359613 | CAAACGCCAGTATAT[A/G]AATTGACAAGCAAAA | 51366 |
rs572561126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102259851 | AGATCATGAGATCAA[A/G]ACCCCGTCTCTACCA | 51366 |
rs572574022 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102347910 | TTTAAAGCCACCTAT[A/G]TATTTCTAATCACAA | 51366 |
rs572604651 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102266968 | CTTTTCTGAGGAGTC[C/T]ACTAATCCAAGATCC | 51366 |
rs572626360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102310653 | CACGCCCAGCCTACA[C/T]TAACCTTTTTATCTG | 51366 |
rs572641479 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102266375 | CTTAGTAAATTAATA[C/T]GAATTTAGTAGGCAA | 51366 |
rs572651336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102354860 | CTGGCCGGGCATAGT[A/G]GCTCATGCCTGTTAC | 51366 |
rs572661761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102317124 | CAGCCGAAGCAGGGC[A/G]AGGCATTGCCTCACT | 51366 |
rs572681954 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102387435 | GTTCCTGGTCAGGGG[C/T]GGTGGCTCATGCCTG | 51366 |
rs572694337 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102385460 | ATCAAAAATACCTAC[-/A]AAAAAGTATAATTAA | 51366 |
rs572716001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102361829 | CCCTCACCACCCCAT[C/T]TGCAACCTCAGTAAC | 51366 |
rs572722751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102257487 | TTATAGAGCAGAAAA[A/G]CAAAAACTGCCTTAT | 51366 |
rs572728106 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102360938 | CTATTCTGTTACTAA[C/T]TAGTTTCACACTCTG | 51366 |
rs572757928 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102402189 | TCACTGCACTCCAGC[C/G]TGAGTGACAGAGTGA | 51366 |
rs572764556 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102384090 | ACCAAAAAAATGGCA[C/T]ATCAACAAGAGTAGG | 51366 |
rs572767462 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102395560 | CAAGTAACTTCCTCT[A/G]CCCTTTTCAAAGGAA | 51366 |
rs572775765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102316015 | GTTTTATTACTTCTA[C/T]TTTTAGTACAAAATC | 51366 |
rs572805049 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102366437 | AGTCTTTCCTTACCC[C/T]TCTGCTTTTCTGGAT | 51366 |
rs572815535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102324838 | AAGACATGAATATTT[C/T]ACTTGTTCTGCAGCT | 51366 |
rs572836043 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102410128 | AAAGCTGATTGTTTA[C/T]ACTAGGAATGGAAAA | 51366 |
rs572837267 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102367460 | CACTCCAGCCCCGCC[C/G]CCAGCAAACTGAGAT | 51366 |
rs572867969 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102290448 | TCGTGGATTACAAAA[G/T]TGGGAAAGGCTAAGA | 51366 |
rs572890514 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102321849 | GGGGAAAGGATTCCC[C/T]ATTTAATAAATGGTG | 51366 |
rs572899785 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | UBR5 | GRCh38.p7 | 8:102301104 | ACATGACATTCTCAT[G/T]TGAAAGACCTAACAC | 51366 |
rs572929867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102294455 | CAAAGCAGACTCAAA[C/T]ATTTATATGAATAAA | 51366 |
rs572965947 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102397124 | ATATCCTATCTTCCC[G/T]CCATCAATGCCTATA | 51366 |
rs572967325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102308704 | TGTACTTCTTCTATC[C/T]ATTTTTTTTAAAGTT | 51366 |
rs572975332 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102359345 | TTTAGTTTAACAGTA[C/T]ATAAACTTTAGATAA | 51366 |
rs572982680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102346528 | GAGGCCAAGGTGGGC[A/G]GATCACCTGAGGTCA | 51366 |
rs573001132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102307974 | ATGATCTTGTTCAAT[A/G]TAATTCCTCTAAATA | 51366 |
rs573004622 | snp | A/T | 0.000100649 | 0.00709327 | intron-variant | UBR5 | GRCh38.p7 | 8:102279227 | AACATAAAAAGATAA[A/T]ATGTTTTGTTTTTTA | 51366 |
rs573035788 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102330561 | CTTCCCTTACCTTTA[A/C]CATGGATGTCTACAA | 51366 |
rs573084987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102315652 | ATTTTCACCAGGATC[C/T]TAACATGAGTGATCT | 51366 |
rs573115074 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102329507 | AATTATGTAAACACA[C/T]AAACCACAACTATAC | 51366 |
rs573129117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102395079 | TCCAGTTCTTAACAC[C/T]TTGTCCTACGTCCTA | 51366 |
rs573135868 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102373811 | ATGGCTTCTTGTTGC[C/G]GTTTTATTAACGTCA | 51366 |
rs573145089 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102344010 | AACACTATTACATAG[C/T]GCATTCAATATATTA | 51366 |
rs573170752 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102367878 | CACACCAGCCTTCTG[C/T]TTGCCTCAGCCCAAG | 51366 |
rs573177275 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102301671 | AAGCTCAACAGACAC[C/G]TGGTATCCTACCTAA | 51366 |
rs573211249 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102391797 | GACCTACTAGGTCGT[A/G]TTCCCAGACAGTTAG | 51366 |
rs573228921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102335838 | ACAGGCGTGAGCCAC[C/T]GCGCCTGGCCCAAGT | 51366 |
rs573243701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102401100 | AAAGCCACCACAATC[C/T]ATGATTTTACTACAA | 51366 |
rs573254781 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102351104 | GTGGGATTGTAAAAC[C/G]GAACAACCACTTTCG | 51366 |
rs573282566 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102326086 | CAGAAAATAGTACCC[A/G]TAGAAGCCTAAAACC | 51366 |
rs573330170 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102393273 | CTGGTCAATTTACTA[C/G]GGGAAAAAAAGGGCT | 51366 |
rs573336176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102400673 | GACTGTGACCTTACA[A/G]GCACCGAAATGCATT | 51366 |
rs573336560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102321151 | GGAAGTCAAATTGTC[C/T]CTGTTTGCAGATGAC | 51366 |
rs573341278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102358477 | TGGCAACAGTATAAC[C/T]GGTAATACTTATTCT | 51366 |
rs573396770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102386649 | CACAGTCCTTTACTA[C/T]GACATTCTGTTTTTA | 51366 |
rs573403629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102285868 | CTTACGTAAATCTAA[A/G]TGGTCAATTGTGGTA | 51366 |
rs573409422 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102318256 | TAAAGGAGCTGATGG[A/G]GCTGAAAGCCAAGGC | 51366 |
rs573410727 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102386025 | ATGATTCTAATATGA[A/T]GTGCATAGTCCACCA | 51366 |
rs573412054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102373782 | GAGAGTTTCTTTGTA[C/T]GAGATTTACTGAGAT | 51366 |
rs573412583 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBR5 | GRCh38.p7 | 8:102285069 | AACAAACAAAAAATT[A/G]TAAGTTGAGGATCCA | 51366 |
rs573459975 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102407823 | TTTTCACTTATTTTT[A/C]CAACCAAATGCATTG | 51366 |
rs573490194 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102306048 | CTATTAAAGGTTATA[C/T]GAAAACCGATACCTT | 51366 |
rs573512395 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102381388 | AACAAACAAAACCAT[A/C]AGATCTCATGAGAAC | 51366 |
rs573526899 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | UBR5 | GRCh38.p7 | 8:102313743 | ATCAACCACAAATCC[A/C]TGGATAACCAATATC | 51366 |
rs573575055 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102380560 | TAGCGAAAAAGCATT[A/C]ATAGGGATAGAGACT | 51366 |
rs573625993 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102276471 | CTATTAGTAATAACA[A/T]ACAGCTTTTTAGCTG | 51366 |
rs573632252 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102414679 | GCTGGGATTACAGGC[A/G]CTGCCACCATGCCTG | 51366 |
rs573689132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102334713 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT | 51366 |
rs573695565 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102384529 | AACATAATGAGACCC[C/T]GTCTCTACAAAAAAT | 51366 |
rs573709329 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102369730 | TTATGCTCAAAGGTA[C/T]AGATTTAATACAGTT | 51366 |
rs573709919 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102410446 | TTTCTAAATTTTACC[A/G]AAAAATTTTATGTTA | 51366 |
rs573723368 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102290082 | AAGTTTCACTTCCCT[A/T]AACACCTGATTTGGA | 51366 |
rs573728233 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102263280 | CTCAATCCCAGCTAC[G/T]CGGGAGGCTAACTCA | 51366 |
rs573738965 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102362678 | AAACTGCCACAAAGC[A/T]TATATAATCTAACTT | 51366 |
rs573752359 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102334316 | TTTAGCGGGGAAACA[C/G]AACCTCACTCTGTCG | 51366 |
rs573756416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102270640 | TTCTCCTGCCTCAGC[C/T]TCCCAAGTAGCTGGG | 51366 |
rs573777047 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102319665 | CACACCACACCTATT[C/G]CAAAACTGACCACAT | 51366 |
rs573782708 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102278446 | TAGTCAACAAATATT[A/G]GGTATCATTATTAAT | 51366 |
rs573790449 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102262380 | AATTATGGGGAGCAG[C/G]CGGCTCTGAACTTAA | 51366 |
rs573861482 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102357636 | CTGGACTGAATCCTG[C/G]ACAAAAGGGTATTAG | 51366 |
rs573868768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102269778 | TGCACAGCAAATTCT[C/T]TAGCATGCAAGGAAG | 51366 |
rs573895329 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102371641 | TCGCCCAGGCTGGAG[A/T]GCAATGGCACGATCT | 51366 |
rs573922186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102364893 | AGGCCTGTGATAACA[C/T]TCGTTTAAATTTGCT | 51366 |
rs573936593 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102364336 | ACAGGTGCGCACCAT[C/T]TCACCCAGCTAATTT | 51366 |
rs573942264 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | UBR5 | GRCh38.p7 | 8:102318370 | TGAATGAAATGAAGC[A/G]AGAAGAGAAGTTTAG | 51366 |
rs573945393 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102253659 | GCATTGGCCCCATCA[C/T]ATGTACAAAAAAAGT | 51366 |
rs573980065 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | UBR5 | GRCh38.p7 | 8:102267900 | CTTCCCTTTTTTTTT[C/T]TTTTTTTTTGAGACA | 51366 |
rs573981123 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBR5 | GRCh38.p7 | 8:102252810 | AGGAAGTTATATAAT[A/G]AAAGCATAGTGCCTT | 51366 |
rs573994373 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102370964 | TTATTTTTTATGGCT[G/T]AATAGTATTCCACTG | 51366 |
rs574005475 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102317707 | GTAGGGGCAGACTGA[C/T]ACCTCACACGGCCGG | 51366 |
rs574040556 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102413920 | GAGTTCGAGACCAGC[C/T]TAGCCAACTTGGTGA | 51366 |
rs574051959 | snp | A/G | 4.97624e-05 | 0.00498786 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295323 | ATCATGATCTGGCAT[A/G]TCTGAATCTAAAATG | 51366 |
rs574078325 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102274501 | CTTTGGGAGGCCAAG[G/T]CAGGTGGATTACTTG | 51366 |
rs574101868 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102412835 | AAACGGGCGGCAAGG[C/T]CCCCTCGATTGGGCT | 51366 |
rs574120423 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102399878 | TTGAACCCAGGAGGT[A/G]GGGGTTGCAGTGAGC | 51366 |
rs574136487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102349901 | TAGTGGCTCATGTCT[A/G]TAATCCCAGCACTTT | 51366 |
rs574153462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102297748 | GTGATATACAAAGAT[A/G]ACATGCAAAGAAATC | 51366 |
rs574161923 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102311081 | ATTTATATCTCTCCC[A/C]TTTGTGCTCCTACAA | 51366 |
rs574180160 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102349053 | TCTATAGCCTAAGAA[A/C]TGCCCAAGATAACTT | 51366 |
rs574184691 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102321554 | ATCCCCATCAAGCTA[C/T]CAATTACTTTCTTCA | 51366 |
rs574198982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102310594 | TCAAGTGATCCACCC[C/T]ACACTCTGCCTCCCA | 51366 |
rs574221621 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102396710 | ACATATATATATATA[-/T]TTTTTTTTTTTCTTG | 51366 |
rs574274545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102341193 | AAATAGACACAACTC[C/T]AACATGATCCAGACA | 51366 |
rs574280788 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102395597 | TAAGGCTAAGTTAAT[A/G]TAGGGTGGAGTCTTT | 51366 |
rs574289938 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102333329 | ATTGTTTTTATGAAG[A/T]ACGAATTGCTGCTTC | 51366 |
rs574301022 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102404544 | ATTTCAAGAATCCTG[C/T]CTTATCATCCTTATC | 51366 |
rs574319074 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102406469 | CAGCTAATTTTTGTA[C/T]TTTTAGTAGAGATGG | 51366 |
rs574354895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102304887 | TTTGTATATATCATA[C/T]AGTATTAAACACAAT | 51366 |
rs574396746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102346629 | TGTGGTGGTGCACAC[C/T]CATTAATTCCAGCTA | 51366 |
rs574414028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102401207 | CCATATCATGTCCCC[A/G]ATCCCCAAAAAATGC | 51366 |
rs574455000 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102397783 | AGTAAAAGAAATCAT[C/G]GACAATCATAGATTC | 51366 |
rs574456531 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102404719 | TCGAGACCAGCCTGA[A/C]CAACATGGTCAAACC | 51366 |
rs574492276 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102403965 | GGTAGCCAGGACCTA[C/G]CCTAGGGGGAAGTGA | 51366 |
rs574507134 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102411392 | CTCGCACCACAGGGG[A/C/T]TAGTAGCAGGAGCTG | 51366 |
rs574522723 | snp | A/T | | | utr-variant-3-prime, downstream-variant-500B | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102252281 | AGAGAACTTTATTTT[A/T]CATGTCTTTATTTTA | 51366 |
rs574543995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102286072 | TGGGAGCCAAGGGGA[A/G]GGGAAGAAGGGTGAG | 51366 |
rs574545452 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102325154 | AGGAGGGAAGGAGGG[A/G]CAAAGAGAGGAGCAG | 51366 |
rs574552713 | in-del | -/CTT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102308693 | TTACTTTAGAATGTA[-/CTT]CTTCTATCTATTTTT | 51366 |
rs574565454 | in-del | -/TT | 0.474544 | 0.10991 | intron-variant | UBR5 | GRCh38.p7 | 8:102380720 | AAAAATTTAACATGC[-/TT]TTTTTTTTTTTTTTT | 51366 |
rs574575963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102376739 | TCGAACTCCTGACCT[C/T]GTGATCTGCCCGCCT | 51366 |
rs574605711 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102360823 | GAGATGGGGAAATAT[A/G]ACATACATAACATTA | 51366 |
rs574619396 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102409371 | ACACTTGAGACATCA[C/G]ACTATGATGCTGAAC | 51366 |
rs574641223 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102384502 | GTCCATGAGTTTGAG[A/G]CTAATGTGGGCAACA | 51366 |
rs574675822 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102296236 | GGAAAACAAAAAATA[C/T]CAACCAGAATTCTTT | 51366 |
rs574679334 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102282191 | AAACAAACAAACAAA[C/T]AAACACCCAGATATA | 51366 |
rs574697594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102281697 | TACTTTGTATAGAAA[A/G]GGAATTCCAGTATCC | 51366 |
rs574719733 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102316798 | GGAGAGAGAATGTCG[C/G]CTTAATAGCAAGGCT | 51366 |
rs574737759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102288621 | AGAATTGCTTGAACC[C/T]GGGAGGTGGGGGTTG | 51366 |
rs574740360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102330975 | CTTCCCCTCCTCAGC[C/T]TATTCAACATGAAGA | 51366 |
rs574743598 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102389783 | TTTTTTTTTTTGAGA[C/G]AGAGTCTCCTCTGTC | 51366 |
rs574769314 | in-del | -/GCTA | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102341013 | GCCAGGCCAACAACG[-/GCTA]GCTAAATCTAACAGA | 51366 |
rs574780593 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102391836 | AGTCACAGGATGAGA[C/T]AGAAGGTCAGCACAA | 51366 |
rs574792125 | in-del | -/AT | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102388017 | TGTGATGTATAAAAC[-/AT]GTGTAAAACACACGC | 51366 |
rs574820540 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102279861 | TAATAAGAAACTGGA[A/C/G]AATGCATTATTTAGT | 51366 |
rs574897909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102337571 | ACATGATCTATCACA[C/T]TGATTAATGTGTATA | 51366 |
rs574898338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102411390 | AGCTCGCACCACAGG[A/G]GCTAGTAGCAGGAGC | 51366 |
rs574907041 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102400469 | CACACCAGCTATCCC[G/T]GGCCTAGCACACTTT | 51366 |
rs574917300 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102373861 | GCTGCCTTTGAAATG[A/G]TCACTTTACGTCCTA | 51366 |
rs574927855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102374476 | TCTCTCTTCCAGAAG[A/G]AGCCTGTACTCCAAA | 51366 |
rs574961337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102345653 | CTAGGGAATGACATC[A/G]CCTGAGGAAAAACAC | 51366 |
rs574989803 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102373702 | AATGAAATCTGATTT[A/C]TCTATAGAAACAAGA | 51366 |
rs575020665 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102273470 | CATTCTCACATTGAT[A/G]GTGAAAATGCAAAAT | 51366 |
rs575027339 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102358571 | ATTTTCAGAATTCTT[C/T]ATCATATACTGTGTG | 51366 |
rs575067281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102395962 | TTTTGCTTTATCATA[C/T]ACTTGATAAAGCTGC | 51366 |
rs575072083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102375614 | CATAGTTGTGGGATA[C/T]TCTCCCAGTCCTCTT | 51366 |
rs575082658 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102383440 | CAGAAGAAAAAGTGA[A/C]AGCTGTCTGCTGAAA | 51366 |
rs575088164 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102404526 | CCATGGAAAAATCAC[C/T]GAATTTCAAGAATCC | 51366 |
rs575134620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102321815 | CTGATCTTTGACAAA[C/T]CTGAGAAAAACAAGC | 51366 |
rs575135168 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102257375 | ATAAAAAGCCATGTT[A/G]CAACAGTAAACTGGT | 51366 |
rs575138585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102408837 | TGGAATGGAGCCCTG[A/G]ACTTTAAAGAAAAGT | 51366 |
rs575144058 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102271587 | CATGACTAGACTCAT[A/T]TAAATATCCTCTGTT | 51366 |
rs575147352 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102377418 | ATCGTTAAAAAATGT[A/G]CAATACTGGCCAGGC | 51366 |
rs575149104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102272259 | AATTTTTATATCACT[A/G]TGTATTTTACAACCT | 51366 |
rs575152391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102321037 | TGGCACAAGACAGGG[A/G]TGTCCTCTCTCACCA | 51366 |
rs575177340 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102264617 | TACATATATCCCCCC[A/C]CACATAATACGTATT | 51366 |
rs575250380 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102380477 | AGCAGAAATAAGTCT[A/G]CTTATTCAAATAGAT | 51366 |
rs575279058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102350309 | TTGAAGGATTCACAC[C/T]TCACAATTTCAAAGC | 51366 |
rs575303762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102314402 | TACAAATTTTGAGCA[A/G]AAGTTGTGACCAAGA | 51366 |
rs575333180 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102277279 | AATACAGGAATCATA[C/T]GCAAGTTTTTTTTCC | 51366 |
rs575340447 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102313596 | CAACATATCATCACA[A/T]ATGCTCAAAGAGAGG | 51366 |
rs575367143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102402653 | AAATGAATTTCCACC[A/G]TGTCCCTAAGTAAGA | 51366 |
rs575393261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102352361 | TTTTACTTCATAGTT[C/T]CCTATGAGTTTTAAA | 51366 |
rs575402878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102261810 | CTATGTGTACACACA[C/T]GTTCATCTCTTTCAT | 51366 |
rs575405429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102359508 | AAAGTAATAAATAAC[A/G]TTTAATTACATCATT | 51366 |
rs575496455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102344978 | TCTATTCATTTAATA[C/T]TGGTCCTAAATCCAT | 51366 |
rs575497295 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102316086 | AAGACAGAGAAAGAA[C/T]ACGAAAACTAAAAGC | 51366 |
rs575497826 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102409324 | CACAAATTATGAAAA[A/C]AAGATACTTTTTTAT | 51366 |
rs575498639 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102308896 | ACCCTGCAGTAAAAT[C/G]TCACATGTACTCCCA | 51366 |
rs575515927 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102358793 | TTTTTTTTTTTGAGA[C/T]GGGGGTCTCTCATTT | 51366 |
rs575555660 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102362639 | TCCAAAAATAAATGA[C/T]GTTAAAGCCAGTTTA | 51366 |
rs575565647 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBR5 | GRCh38.p7 | 8:102407776 | AAAAAAAAAAGAACG[C/T]ATATTGCTTGAAATA | 51366 |
rs575577751 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | UBR5 | GRCh38.p7 | 8:102309418 | TTAAAAAAAATTTAG[A/T]GTAGCCTAAGTGTAC | 51366 |
rs575598581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102357524 | GAGTTATCATTGTGC[C/T]ACTGCCCTCTGGCCT | 51366 |
rs575616170 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102315927 | TAAATTCCATATTCT[A/G/T]TTCTAATCTTGTATT | 51366 |
rs575634258 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102254879 | GCCAAACAAAAGATA[C/T]GGTCTTAGGTTCAAA | 51366 |
rs575650800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102357025 | CCCACAAAATGCATA[C/T]TAAAGAAAAATGGGA | 51366 |
rs575660977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102307113 | CTGTGTGTAAAAGAG[A/G]TAACAGAAGCTGTAT | 51366 |
rs575663506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102400430 | AACCCGAAGTTTCAG[A/G]ACGGTTTGGTGTGGC | 51366 |
rs575688693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102340274 | CATGACATTCAAACT[A/G]TCTTGAGCTAGGAAT | 51366 |
rs575693424 | snp | G/T | 0.000181227 | 0.00951738 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102289551 | GTGGATTCCTGATGA[G/T]GTAGGATGACTGAGA | 51366 |
rs575717304 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102388301 | CCACACCCAAAAGAT[A/T]TTTGGAGTTTTCCTT | 51366 |
rs575733824 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102370986 | ATTCCACTGTATATA[C/T]ACACCACATTTTTAA | 51366 |
rs575740188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102407149 | GAGTCTTGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 51366 |
rs575760602 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102395316 | CACCAGACACCCAAG[A/G]CTAGAACTGACAGGC | 51366 |
rs575768924 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102364728 | AAGAGAGTTATGACT[A/G]AACTGGGCCCTACAA | 51366 |
rs575774039 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102399002 | AAAAGACATATAAAT[A/G]GCAAACAGGTATATG | 51366 |
rs575788747 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102318974 | CAACCGGTACCAGCC[A/G]CTGCAAAATCATGCC | 51366 |
rs575790154 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102328268 | GAGTTTGAGACTAGC[A/C]TGAGCAACACAGTAA | 51366 |
rs575802403 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102335418 | GTTAAGTAGATTTTA[C/G]CTGCTCTTGTCACAA | 51366 |
rs575835100 | in-del | -/A | 0.00716266 | 0.059414 | intron-variant | UBR5 | GRCh38.p7 | 8:102263198 | TATAATGTTGATAAG[-/A]AAAAACTGGTTTCAT | 51366 |
rs575861864 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102335173 | CAGGGAAAAAACATA[G/T]TGTGTGATCTCACTT | 51366 |
rs575862230 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102318493 | GTGATGGGGAGAATG[C/G]AACCAAGTTGGAAAA | 51366 |
rs575902778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102306407 | CCCCAACTTGAGAGC[A/G]GGTGGAGAACAGATG | 51366 |
rs575930731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102292451 | ACAAGATGACACAAA[A/G]TCTTGAAACTTAGTA | 51366 |
rs575933472 | in-del | -/TAT | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102337354 | CTGCCTTGCATTAAA[-/TAT]TATTGGAAAAGCTCT | 51366 |
rs575935422 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102285031 | AAGAGTGTGAGACTC[C/T]GTCTCAAAAAAACAA | 51366 |
rs575939488 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102278747 | AATATTCTGAATTAA[C/T]GCATTTCTAAAAATC | 51366 |
rs575958810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102385962 | CACAAACTTTCTCAC[C/T]CAAACACATAAAAGA | 51366 |
rs576048380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102394276 | ATTTTGGTCAGGCTG[A/G]TCTCTTAACTCCTGA | 51366 |
rs576063206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102369448 | GACACAGATACTCAA[A/G]AATCACATTTGCTAA | 51366 |
rs576097701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102391949 | GTAAGTGACCTCTGG[C/T]AATCCTCACTGCTAT | 51366 |
rs576099904 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102306322 | ATGTGGGAGTATAAA[A/G]GAAAAAAAAAAACTG | 51366 |
rs576115750 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102341051 | ACAATGGCTAGGCTT[C/G]CTAAACTTACACTAT | 51366 |
rs576125033 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102376649 | GCTAGGATTACAGGC[G/T]CCCGCTACCACACCT | 51366 |
rs576144715 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102367065 | TCTTGCCTATACCAT[-/T]TTTTTTTTTTTTGGA | 51366 |
rs576147678 | snp | A/C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102414659 | CTGCCTCAGCCTCCC[A/C/G]AGTAGCTGGGATTAC | 51366 |
rs576167484 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102276419 | CCTTTCTAAAGCCAA[C/G]ATTCTGCCTCAGCAT | 51366 |
rs576175090 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102340120 | TCATAAGACAGGCTC[A/C]ATATCCGATCTTGTG | 51366 |
rs576177562 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102327417 | CAATTATGTAAAAGC[A/C]AAGTACATGTTTATG | 51366 |
rs576184401 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102398526 | GGTGGCTCATGCCTG[G/T]AATCCCAGCACTTTG | 51366 |
rs576248552 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102378928 | GCCTTTTAGATAGTG[A/C]ATGGATATGACAGTA | 51366 |
rs576256615 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102283476 | ACACTTTAAATGGGT[A/G]AATTATATGTGATAT | 51366 |
rs576270550 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102260937 | ACTTTCTCACAATGA[C/T]GTGGTTTTTCCAAGT | 51366 |
rs576306927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102260301 | TGGAATTTCAGTAAT[C/T]ATGGCTGGTTGTGCA | 51366 |
rs576315254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102268718 | CCAGGAGGGTATTCT[A/G]ATAAGTGAATTTGAG | 51366 |
rs576329726 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102274867 | AGAACAAAAAAAATG[C/T]ATTCCCAAACTGTTA | 51366 |
rs576338599 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102371624 | CACGGAGTCTCGCTC[C/T]GTCGCCCAGGCTGGA | 51366 |
rs576348182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102412051 | GTAAGGACCCCCGCA[C/T]CCCACCCCAGCTGGC | 51366 |
rs576349905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102370297 | TCAGCCTCCTAAGTA[A/G]CTGAGATTACAAGCA | 51366 |
rs576357699 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102405038 | TCAAATTTTTTAACA[G/T]GTTAGAACCCAATCA | 51366 |
rs576399439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102371066 | ATTGTGACTAGTGCT[A/G]CGATAAACATCTCTT | 51366 |
rs576409314 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102378333 | GTACAAAAGTAATTG[C/T]AGTTTTGCCATTAAA | 51366 |
rs576414672 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102354003 | GCCACTGCATTCCAA[C/G]CCGGGTGACAGAGCC | 51366 |
rs576479250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102353400 | CTAGTATGGAATTAG[C/T]CCACAGCTTGCAAAC | 51366 |
rs576483316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102384318 | TTAAAGGTATTATTT[A/G]TGTTTAAAATGTATA | 51366 |
rs576496244 | in-del | -/AC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102270988 | TATTGTATTTTATTA[-/AC]AGACTATTCTTAGTT | 51366 |
rs576500233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102317392 | GGCTGGGGGAGGGGC[A/G]CCCACCATTGCCCAG | 51366 |
rs576501863 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102317079 | TGCCAGACAGTAGGC[A/G]CAGGACAGTGGGTGC | 51366 |
rs576509894 | snp | C/T | 0 | 0 | intron-variant | UBR5 | GRCh38.p7 | 8:102332753 | ATACTTTCAGCCTAG[C/T]ACTGATCACATTATG | 51366 |
rs576511418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102406388 | AACCTCCACCTCCCA[A/G]GTTCAAGCAATTCTC | 51366 |
rs576522652 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102324933 | ATTTTCATATGTTAT[A/C]TTTCGGCAATTTAGT | 51366 |
rs576537723 | in-del | -/AA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102273638 | ACTATCTGTAATAGC[-/AA]AAGACTGGAAACAAG | 51366 |
rs576614056 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102300501 | AAAGTTTCTATCCCC[C/T]GTTTATAATCGGTAA | 51366 |
rs576638775 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102362591 | AATCAAATTTCAATC[A/G]TTTGTACTAACAGAC | 51366 |
rs576671652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102311236 | TTGTTGCAAGATCTA[C/T]TCAAGACTATTTAGT | 51366 |
rs576688077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102361922 | AGTTTATAGAAAAGG[C/T]AGCATAAAGTTGGTA | 51366 |
rs576729648 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBR5 | GRCh38.p7 | 8:102259485 | TCAGGAAAGATAAAT[G/T]GACAACAACAAACCT | 51366 |
rs576735385 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102385017 | GGCATCAACAGGGTA[C/T]TACAGCACATAATAT | 51366 |
rs576744692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303268 | AATTTGGTCACCCAT[A/G]AATACTTTTTGATAA | 51366 |
rs576756355 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102310504 | GGCGTGCGCCACCAT[C/G]CCGGGCTAATTTTTG | 51366 |
rs576806757 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102404902 | ACAAGAGCGAAACTC[C/T]ATCTCAAAAAAAAAA | 51366 |
rs576806978 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102258606 | AATCATCATACAAAT[G/T]CTTTCATTAGGGAGT | 51366 |
rs576823409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102360234 | AAGACCAACATTTTT[C/T]ACAACCCTGTTATTT | 51366 |
rs576827571 | in-del | -/T | 0.185472 | 0.241529 | intron-variant | UBR5 | GRCh38.p7 | 8:102290895 | TGTTTTGATCTTGGG[-/T]TTTTTTTTTTTTTTT | 51366 |
rs576831562 | snp | C/T | | | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102259015 | AAGAGGTAAAACTGA[C/T]CAGCATTTGCACATT | 51366 |
rs576834103 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102368635 | GGGTGGGTGAGGGTA[G/T]GGGGGAGGTGTCTTG | 51366 |
rs576835761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102310115 | CCTTTTCCCTTATCC[C/T]ATTTGTTCCCCCTCC | 51366 |
rs576874247 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303664 | CACATCACCCTTTCA[-/T]TTTTTTCCCAGATCA | 51366 |
rs576888914 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBR5 | GRCh38.p7 | 8:102292721 | GATACACAGCTTGAT[C/T]TGTAACAGTTTTCAA | 51366 |
rs576889719 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102367687 | GAACAATGCCTTTCC[C/T]CCATGCACTCTGTAT | 51366 |
rs576891718 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102410329 | TAATATAGAAAACAT[A/G]CCCTACCTCTCTTCT | 51366 |
rs576930928 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102402918 | ATCACAGTGCTTTGT[C/G/T]GACTAGCCACTATCA | 51366 |
rs576933250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102391206 | ACAATTGTGCTTTAA[C/T]ATAGAATGTCAACAT | 51366 |
rs576934275 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102290435 | GGTAAAACAGAGATC[C/G]TGGATTACAAAAGTG | 51366 |
rs576947156 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102262943 | ATACAAAAATTAGCC[A/G]GGCATGGTTGTATGC | 51366 |
rs576959468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102338888 | TTACGTATGTATGTA[C/T]GGAAACCTATTATGG | 51366 |
rs576962115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102401774 | GTCCCACTGCCCATA[C/T]TCCCCCTACTCAATT | 51366 |
rs576967572 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102325931 | AGCTAATTCAGCTAA[C/T]AGGAAGCTAATTCAG | 51366 |
rs576972309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102300321 | GAATAAGTCAGTGAG[A/G]GATAGAAATAAAACT | 51366 |
rs576976876 | in-del | -/A | 0.390651 | 0.206682 | intron-variant | UBR5 | GRCh38.p7 | 8:102378657 | CTTGAAAAAAGGAGG[-/A]AAAAAAAAAAAAAAA | 51366 |
rs576978306 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102322834 | TCTCAGTAAATTATC[G/T]CAAGGACAAAAAACC | 51366 |
rs576995237 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102265358 | TCTCTCAAATCATTC[A/T]AATGAAGTCAGGTAG | 51366 |
rs576995748 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102343435 | TAAGACTAGGATAAA[C/T]AAGGATTAGAAACAA | 51366 |
rs577017193 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102316119 | AACCTTAATGAGGTA[A/T]AAAGTGCAATAGCTT | 51366 |
rs577021676 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102288350 | GAGAATTTGAAATCA[C/T]ATATCAAGCAGTTTT | 51366 |
rs577041780 | snp | A/G | 0 | 0 | intron-variant | UBR5 | GRCh38.p7 | 8:102390773 | CTGACAATACCATGT[A/G]GTCCAACGCAAAATA | 51366 |
rs577041879 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102322215 | GGCTAATATTCAGAA[C/T]CTACAATGAACTTAA | 51366 |
rs577058082 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102394040 | GTGAATAGTTAAATA[A/G]GCTAAAACACTTTCC | 51366 |
rs577085012 | in-del | -/AG | | | intron-variant | UBR5 | GRCh38.p7 | 8:102364714 | TCCTTTCAAATCTCA[-/AG]AGAGTTATGACTAAA | 51366 |
rs577129051 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102389075 | TTCTAAATAATTATG[C/T]TTTACTATTATCACT | 51366 |
rs577135203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102287881 | TATTTTCCTTTTCTC[C/T]AATTTCCAAATGTTT | 51366 |
rs577135255 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102296050 | TCCCAGTCCTGTTCA[A/C]GTGGTCCTCCTATAT | 51366 |
rs577187862 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | UBR5 | GRCh38.p7 | 8:102270770 | ATGATCCACCCACCT[C/G/T]GGCCTCCCAAAGTGC | 51366 |
rs577231276 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102299177 | ATCAGGCATAAGCTA[C/T]CAGAACAATATTCTA | 51366 |
rs577305515 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102395102 | ACGTCCTACATCCTA[C/G]AGCTCTCCCACCAGC | 51366 |
rs577307576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102379683 | AAAAGGAAAAAAATA[C/T]AAGAAACACTTCTTA | 51366 |
rs577315415 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102309299 | GCCTCAAGGGATCCA[A/T]CCACTTTGGCCTCCC | 51366 |
rs577320066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102379121 | GTTTATTGGTATCAT[C/T]AGCTACCTCCTCTCT | 51366 |
rs577349259 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102310996 | CCAACTCCATCCCTG[C/T]GTCTAAGGGGCCTAT | 51366 |
rs577368017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102401199 | AAGCTTAACCATATC[A/G]TGTCCCCGATCCCCA | 51366 |
rs577375963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102352265 | AGTGAGCCAAGATCG[C/T]ACCACTGCACTCCAG | 51366 |
rs577384855 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBR5 | GRCh38.p7 | 8:102330912 | AGTTCTCTTCAGCCT[C/T]TGCCATCCTTGAGAC | 51366 |
rs577424871 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102261116 | CAAATAGCCTCATTG[C/G]ATCACACAACACTTT | 51366 |
rs577462137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102286697 | CCTCATTCAGGAAAA[C/T]ATACATATTAAACAG | 51366 |
rs577464017 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102296627 | TATACTTCTCAAAAG[A/G]CTAATCTGATCCTAG | 51366 |
rs577467325 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102352963 | GACAACCGTCAAAAT[A/C/G]TCTCTCCAGTTTCTC | 51366 |
rs577471897 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102353171 | TCTAATAGAGGTCTA[C/T]TGGTAGTCACAAAAG | 51366 |
rs577483335 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | UBR5 | GRCh38.p7 | 8:102264716 | AAAAACAAAACAAAA[A/C]AAAAAAAAACAGGAA | 51366 |
rs577499606 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102285934 | TGGGGAGAGGAGTAT[A/G]GAGGGGACAAGAATT | 51366 |
rs577509082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102271535 | ATAGCAAGTAAGGTT[A/G]TGATAGTGTCACTAT | 51366 |
rs577522521 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102272415 | TCAATCTAGAATAAA[A/T]GTATGTAAAAATGCA | 51366 |
rs577549192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102375154 | TCACTTGAGGCCAGG[A/G]ATTCGAGAACAGCCT | 51366 |
rs577609492 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102374621 | GAAAGCAGGTACGTA[C/G]GTAGGTAGGTGACAT | 51366 |
rs577661084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102284527 | TTAAGTAATGCAAGC[A/G]AGTCATTTCTTTCTC | 51366 |
rs577666330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102319825 | AAAACTGAACAACCT[A/G]CTCCTGAATGACTAC | 51366 |
rs577695535 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102335266 | GTTACCATGGGCTGA[A/C]AAGCAGTGTGGGGGT | 51366 |
rs577800799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102358647 | GAGCTATATTTAGTA[C/T]AGCTAAAGGATGTAC | 51366 |
rs577809815 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102268013 | TCTCCCTGCCTCAGC[C/T]TCTCGAGTAGCTGGG | 51366 |
rs577810352 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102255933 | ATTTTGAGGTCTTTA[C/G/T]AGAAGGAGATTTTCT | 51366 |
rs577811404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102365418 | CCAGGATCAGTGAGC[C/T]GAGATCGCGCCACCG | 51366 |
rs577840552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102308107 | CAGATAATCTTCTAA[C/T]AGACAACTTAAATTT | 51366 |
rs577849179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102263439 | TTCCATTTGTTTTGT[A/G]TCAAGTAATTTCTCT | 51366 |
rs577880989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102350055 | CAGGCATGGTGGAAC[A/G]TGTCAATGGTCTCAG | 51366 |
rs577890305 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102351853 | AATCAACTACTTGTG[C/T]GCCTACAGTCCCAGC | 51366 |
rs577893280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102364991 | TTCTATACAACAGAG[A/G]TTCACCTACTTTAAA | 51366 |
rs577911188 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBR5 | GRCh38.p7 | 8:102399298 | TTTTTTTTTTGAGAC[A/G]GAGTCTCACTCTGTC | 51366 |
rs577930407 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102383742 | TGACACGAGCTTCCA[C/G]AATAAAAGGACCCAT | 51366 |
rs577938387 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102253753 | TCAATGCAGTCAAAC[C/T]GCAATAAAAGTGGTT | 51366 |
rs577956855 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | UBR5 | GRCh38.p7 | 8:102318203 | TGAAAAAAATTTAGA[C/T]GAATGTATAACTAGA | 51366 |
rs577974555 | snp | A/T | 0.00874735 | 0.0655527 | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102414540 | AGATCTAAAAAAAAT[A/T]TTTTTTTTTTGAGAC | 51366 |
rs577975387 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102261764 | TCACTAACTCTTGAT[A/C]CATCTTTAACACCGA | 51366 |
rs578024856 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102312735 | GTGAATGTTTTCAGT[A/C]ATCAACTGAAAAACT | 51366 |
rs578028496 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | UBR5 | GRCh38.p7 | 8:102320841 | AAGACAAAAACCACA[A/T]GATTATCTCAATAGA | 51366 |
rs578037436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102407062 | ATGTGACTAGCTACA[A/G]ATGAAGTGACTTAAA | 51366 |
rs578057472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102318408 | AGAATAAAAAGAAAC[A/G]AACAAAGCCTCCAAG | 51366 |
rs578083259 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBR5 | GRCh38.p7 | 8:102406584 | CAGGCATGAGCCACC[A/G]CACCTGGCATAATGC | 51366 |
rs578127407 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBR5 | GRCh38.p7 | 8:102342100 | GTGTCCACCTGACTT[C/T]AGAAATTTGACAAAA | 51366 |
rs578159668 | in-del | -/TC | 0.00119737 | 0.0244387 | intron-variant | UBR5 | GRCh38.p7 | 8:102283567 | ATCCGCTATCAGAAT[-/TC]TGTGTTCTCTGGGGT | 51366 |
rs578165641 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102275977 | TGTCCTAACAGAGAA[C/G]TTTTCCATAGCTACT | 51366 |
rs578173678 | snp | A/G | 3.31735e-05 | 0.00407255 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295204 | TTAATGAATACGTAC[A/G]GGTCTTTATTCTCCT | 51366 |
rs578179950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102393501 | ATTAGCCACGCATGG[C/T]AGCACACGCCAGTAG | 51366 |
rs578240785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR5 | GRCh38.p7 | 8:102393680 | CATGCCTGTAATCCC[A/G]GCACTTTGAGAGGCT | 51366 |
rs578256316 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102367220 | AGTCCTCAATTTTTA[C/G]ACAGTTCTTTTAAAC | 51366 |
rs745326379 | snp | C/T | 0.000165172 | 0.00908618 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311855 | AAAGATACAGTATCG[C/T]ACCCAATTTCCAGTC | 51366 |
rs745343443 | snp | A/G | 0.00017477 | 0.00934636 | intron-variant | UBR5 | GRCh38.p7 | 8:102261902 | GAATCAGAAAAGTGT[A/G]TATTTGCTTTACCTG | 51366 |
rs745353201 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102343182 | AATATAAGCTAATTA[C/T]AAAGTTTTTAAAAAT | 51366 |
rs745389835 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102355073 | GTCAAGGCTGCAGTG[G/T]GTCAAGATCACATGA | 51366 |
rs745417613 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102385249 | TACACCCCAATAAAA[A/G]ATAAGCACTGAAAGA | 51366 |
rs745421543 | snp | C/T | 1.66158e-05 | 0.0028823 | intron-variant | UBR5 | GRCh38.p7 | 8:102361100 | GTTTATTTTTCATTT[C/T]TGTATCTTAGAGTGA | 51366 |
rs745433446 | snp | A/G | 1.68935e-05 | 0.00290628 | intron-variant | UBR5 | GRCh38.p7 | 8:102285381 | AACTATCCAAATAGA[A/G]CTAAATTCGATACAG | 51366 |
rs745440733 | in-del | -/ACATAT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102396664 | TACACACACACACAC[-/ACATAT]ATATATATATACACA | 51366 |
rs745448179 | in-del | -/AG | | | intron-variant | UBR5 | GRCh38.p7 | 8:102314214 | TTATAGTATCTAACC[-/AG]AGTTTAAAAAGGAAG | 51366 |
rs745450965 | snp | A/G | 1.65449e-05 | 0.00287614 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102298920 | TTCAATATAAAATGA[A/G]CATTCGCCTTTCGAT | 51366 |
rs745451253 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102361969 | ACCAAAGGCTCAATT[G/T]TTTAAAAAAACAAAA | 51366 |
rs745495599 | snp | C/T | 1.70577e-05 | 0.00292037 | intron-variant | UBR5 | GRCh38.p7 | 8:102299411 | AAGTGTGTCCTTTTT[C/T]CTTCCAGATGACTAG | 51366 |
rs745520681 | snp | G/T | 1.67494e-05 | 0.00289386 | intron-variant | UBR5 | GRCh38.p7 | 8:102277208 | CTATGAATATTTACA[G/T]TTAAAAGTTACAAAT | 51366 |
rs745526001 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102281134 | GGCAATGGGGAAAGG[C/T]TGGATAAATTCAAGC | 51366 |
rs745526691 | snp | G/T | 5.42746e-05 | 0.00520906 | intron-variant | UBR5 | GRCh38.p7 | 8:102361223 | TGAGAGATAAAAAAA[G/T]AAAAAGTTAAATTAT | 51366 |
rs745530951 | snp | A/T | 9.88549e-05 | 0.00702977 | missense, nc-transcript-variant, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102277109 | TGGCAGCACGGGCTG[A/T]TCTTCCCCTTCTTTT | 51366 |
rs745533186 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102281204 | TTGCAATGCTATTCT[C/T]CTTACTCCAAATGTT | 51366 |
rs745534412 | snp | A/G | 1.64795e-05 | 0.00287045 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102266986 | TAATCCAAGATCCAG[A/G]ATACTATCAGCTCCA | 51366 |
rs745540035 | snp | G/T | 1.65913e-05 | 0.00288017 | intron-variant | UBR5 | GRCh38.p7 | 8:102342453 | TTTAAATGGAAGCAG[G/T]GTGAATTTTTTCCAA | 51366 |
rs745543707 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102374989 | ATTCATGTCTTAGCT[C/T]TAAGCCCTACACTGT | 51366 |
rs745545814 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102386318 | GCCTGTAATCCTAAC[C/T]ACCTGGGAGGCTGAG | 51366 |
rs745583505 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102295846 | ACAAAGGTTTATGTT[A/G]ACATTATGAAGGTAT | 51366 |
rs745588755 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102313529 | TAACGTATCTCTATG[A/C]AACTTTTCTACAAAA | 51366 |
rs745591058 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102301409 | ATATATTTGCCATTA[C/T]AGTATTCACTATTAA | 51366 |
rs745591186 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102372083 | CTCCGGGTTTGACAT[A/G]TAAGAATTAAAGAAT | 51366 |
rs745595060 | snp | A/C | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102342574 | CCTTGCTGGTAGAAC[A/C]CCTTTCATTATCAAA | 51366 |
rs745595183 | snp | C/T | 1.64765e-05 | 0.00287019 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102313906 | TGGTGCAGGGGTTGA[C/T]CGTCGTCGTTCTTAG | 51366 |
rs745610243 | snp | C/T | 1.6604e-05 | 0.00288127 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295270 | CAGTCCTGTAGAACA[C/T]GCTCCAATGCAAGCT | 51366 |
rs745620207 | snp | C/T | 3.30688e-05 | 0.00406612 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102254475 | GCTGGAATCCTTCTT[C/T]ACTGGCTGGCAGTGA | 51366 |
rs745624200 | snp | A/T | 1.64746e-05 | 0.00287002 | intron-variant | UBR5 | GRCh38.p7 | 8:102268973 | TTCCCAATTGTACAC[A/T]TTACCGTCCATGTGC | 51366 |
rs745678818 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102312765 | TTAAGTATATAGCCC[A/G]TGAAATCCTCCCATC | 51366 |
rs745688316 | snp | C/T | 1.65067e-05 | 0.00287282 | intron-variant | UBR5 | GRCh38.p7 | 8:102295380 | ATAAAACATATTGCT[C/T]CCCACAAGTGTCATA | 51366 |
rs745706271 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102319054 | CAAAATAACCAGCTA[A/T]CATCATGACAGGATC | 51366 |
rs745708492 | snp | G/T | 1.74354e-05 | 0.00295253 | intron-variant | UBR5 | GRCh38.p7 | 8:102287601 | GAAAAAAGCACAAAC[G/T]CACTATGGTTTAAAA | 51366 |
rs745719736 | snp | A/G | 1.68315e-05 | 0.00290094 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102314745 | CAAATAAAACTTACT[A/G]TATGGCATTGATGCA | 51366 |
rs745722921 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102381466 | AATCACCTCCCATCG[C/T]GTCCCTCCCTTGACA | 51366 |
rs745734281 | snp | C/T | 1.64917e-05 | 0.00287151 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102281321 | AGGTGTATCCAATGT[C/T]GTCTGCTGATTCATT | 51366 |
rs745749365 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102352105 | TTGAGGTCAGGAGTT[C/T]GGGACCAGCCTAGCC | 51366 |
rs745781572 | snp | C/T | 1.66568e-05 | 0.00288585 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102257684 | ATTGACCAGAACCAA[C/T]GCTTGAACTGCAGAA | 51366 |
rs745790582 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102323996 | AAGAAAATTTGTTTC[C/T]AATATTAAGGAAAAG | 51366 |
rs745810203 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102405961 | AGCAATTAAATTTTC[C/G]TTTGGAAACTATTTC | 51366 |
rs745831740 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102288527 | CAACATGGTGAGACC[C/T]CGACTCTACTAAAAA | 51366 |
rs745840592 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102272251 | ATCGGTGAATTTTTA[-/T]TATCACTATGTATTT | 51366 |
rs745878449 | in-del | -/AAATT | 1.64735e-05 | 0.00286993 | intron-variant | UBR5 | GRCh38.p7 | 8:102254533 | ACAGGAATTTAACAG[-/AAATT]GTTAATATTTAACTC | 51366 |
rs745888496 | snp | A/G | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311396 | CCAAGACTACTAATA[A/G]GTGGAAGATCCAGCC | 51366 |
rs745911530 | snp | A/C | 2.12891e-05 | 0.00326253 | intron-variant | UBR5 | GRCh38.p7 | 8:102297022 | AAAGGAATAATTATA[A/C]GTATGCATATATCTC | 51366 |
rs745911705 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102356473 | AGATAAATAAATAAA[C/T]AATGGGCCGGGTGCA | 51366 |
rs745912942 | in-del | -/TTCTTT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102394368 | TCCGGCCAGAATTTA[-/TTCTTT]TTCTATTATTAAAAT | 51366 |
rs745929715 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102371112 | AATTCTTTTGGACAT[A/G]TACCCAGCAGTGGGA | 51366 |
rs745941415 | snp | C/T | 1.65332e-05 | 0.00287512 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102297572 | AACCATTCCCATGAA[C/T]ACATCTTCCTCTTTT | 51366 |
rs745947022 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102326822 | ATCTTAATTATAATT[C/T]GTGCATTAGATTAAT | 51366 |
rs745989324 | snp | G/T | 1.65302e-05 | 0.00287486 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102275587 | GCGGAATTTTGATTC[G/T]TTTACCTCAAAACCA | 51366 |
rs745999637 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102370387 | GGCCAGGCTGGTCTC[A/G]AACTCCCGAACTCAG | 51366 |
rs746006858 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102413161 | TTGTATTTATGGTGA[A/G]GTTGGTAAAATCAGT | 51366 |
rs746013552 | snp | C/T | 1.67114e-05 | 0.00289057 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102293812 | GCTTGGAATACACGC[C/T]TGCATTTTCCAATTG | 51366 |
rs746031977 | snp | A/T | 1.65258e-05 | 0.00287448 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102293977 | TTTTGGATGAAGCCA[A/T]TTCCACACTCAGAAT | 51366 |
rs746042834 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102296205 | GATTATCACACCTTT[-/A]AGGTACTTAAAATAA | 51366 |
rs746060276 | in-del | -/AA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102386975 | GCAAGACTCCGTCTC[-/AA]AAAAAAAAAAAAAAA | 51366 |
rs746067542 | snp | C/T | 1.76836e-05 | 0.00297347 | intron-variant | UBR5 | GRCh38.p7 | 8:102262094 | GTAATCATATGAAAC[C/T]CAGTTATGAAAGAAA | 51366 |
rs746067959 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102400657 | TCATTTCTCCCAACT[A/G]GACTGTGACCTTACA | 51366 |
rs746072421 | in-del | -/T | 1.72838e-05 | 0.00293966 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303999 | TGCTTTCTGTACTTG[-/T]GTTTTTTCCTCCAAT | 51366 |
rs746075480 | snp | C/T | 1.65031e-05 | 0.00287251 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102275743 | CATCTTCCATGAATA[C/T]CCTGCCGAACAGTTC | 51366 |
rs746081197 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102388156 | TGACCACAAATAATA[C/T]CAAAATACTCTCTTA | 51366 |
rs746107776 | snp | C/T | 4.55394e-05 | 0.00477154 | synonymous-codon, nc-transcript-variant, intron-variant | UBR5 | GRCh38.p7 | 8:102264546 | ATTCTGTAACAGACA[C/T]AGTCCAAGAATCCTA | 51366 |
rs746129897 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102399278 | TATTATCTCATCAAA[A/T]TTTTTTTTTTTTTTG | 51366 |
rs746135986 | snp | A/G | 0.00021418 | 0.0103462 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102329138 | GCTATTTGCAGACAG[A/G]AGGACTATCTTTTCA | 51366 |
rs746137821 | in-del | -/CAG | 1.65176e-05 | 0.00287376 | intron-variant | UBR5 | GRCh38.p7 | 8:102295569 | GAGGAGGGAGGCTGA[-/CAG]AAAGCTACTCAGCTG | 51366 |
rs746152563 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102309187 | CCTGAGCCTCTTAAG[C/T]AGCTGGGATTACAGG | 51366 |
rs746160315 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102298109 | CAAGAGGTTCTATCA[A/G]TAATCCATCTTATTT | 51366 |
rs746171002 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102276324 | TAATGCCCTGACTTA[C/G]ACCAGATTTTAATTT | 51366 |
rs746191175 | snp | C/G | 1.65559e-05 | 0.00287709 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102312345 | CTTTACACTTACCTG[C/G]AATTCATCAATTCTA | 51366 |
rs746229980 | snp | C/G | 0.00280379 | 0.0373367 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102412145 | GGCGCCCCTCCCCCC[C/G]CGCCCGCCGACCCGC | 51366 |
rs746244258 | snp | C/T | 3.32408e-05 | 0.00407668 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102286375 | CTGCTGGTGTAGATG[C/T]ACTGGAAGGGGCTGT | 51366 |
rs746271663 | snp | C/T | 1.70159e-05 | 0.00291679 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102345512 | CTTGGGTGGGCAGAA[C/T]GAATGTCGGCATCAA | 51366 |
rs746275053 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102297353 | AAATCAACTTTCTTC[A/G]TATCAGACTTAATTC | 51366 |
rs746277681 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102377373 | AAGGATTTTTTAAAG[A/G]GCATAATAATCCACT | 51366 |
rs746281406 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102376108 | AGCTCTGACACCGTG[C/T]AACCTTGGATACCTC | 51366 |
rs746282021 | snp | A/G | 1.64762e-05 | 0.00287016 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102286460 | AGCTTGGGCAGCACC[A/G]TTGGCATGGGAGCTA | 51366 |
rs746286476 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102397895 | TGTTAAATGTCTATA[C/T]TACCCAAAGCAATCT | 51366 |
rs746295547 | snp | C/G | 0.000132569 | 0.00814045 | intron-variant | UBR5 | GRCh38.p7 | 8:102278996 | TAAAGAAAATAAACC[C/G]AATTAGAAAGAAACC | 51366 |
rs746326435 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102366167 | ACTGTTAAACAAGGT[A/G]CATCCACTCATGTTT | 51366 |
rs746356491 | snp | C/T | 1.65718e-05 | 0.00287848 | missense, upstream-variant-2KB, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102304146 | GCCTTTCTGCAAATG[C/T]ATTTCTTTCAGAACG | 51366 |
rs746360070 | snp | A/C | 3.32541e-05 | 0.00407749 | intron-variant | UBR5 | GRCh38.p7 | 8:102279214 | AAAGTAGCACCTAAA[A/C]ATAAAAAGATAAAAT | 51366 |
rs746362335 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102407990 | AGCAATGCCCCAGCT[A/G]TGACAATAAAAAATG | 51366 |
rs746376603 | snp | C/T | 1.67189e-05 | 0.00289122 | intron-variant | UBR5 | GRCh38.p7 | 8:102271129 | ATCAAAGATACAAAA[C/T]TTACCTATCCCGGTC | 51366 |
rs746377064 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102406972 | AAGAGAACTTTCAGT[A/G]ATGATGGCACTGCTC | 51366 |
rs746382462 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102378370 | AGAACCAGGTCGGGT[A/G]CGGTGGCTCACACCT | 51366 |
rs746385651 | snp | C/T | 3.29951e-05 | 0.00406159 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102270088 | TCTCCAAGTGCCTGC[C/T]GATGTGCTGGCAAAG | 51366 |
rs746386374 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102291893 | GCCGTAGTTTCCCCA[-/T]TTGACAAACTAGAAT | 51366 |
rs746402597 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102377915 | TTTATTCCCATTAAG[A/C]CAGACTAATCAAGTG | 51366 |
rs746418534 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102315620 | GTTTAGAAATAATCT[A/G]AAAGAAAACTGGTAT | 51366 |
rs746450352 | in-del | -/TATTT | 1.65261e-05 | 0.0028745 | intron-variant | UBR5 | GRCh38.p7 | 8:102329226 | ATAAAAAAAAATTAC[-/TATTT]TATATGTTGATATGT | 51366 |
rs746472020 | snp | A/C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102394011 | ATTCAATGATTTTCA[A/C/T]GTTCTTATTTTAGGT | 51366 |
rs746472094 | snp | A/C | 1.67139e-05 | 0.00289079 | intron-variant | UBR5 | GRCh38.p7 | 8:102299442 | GCAGACAAAGAGTAC[A/C]GATTCTTACCTGGAA | 51366 |
rs746477666 | snp | A/T | 1.65894e-05 | 0.00288 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102312236 | TCGGTGTTCCACCAG[A/T]TTTGACAACCTGCAT | 51366 |
rs746481830 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102404041 | ATGTCCTGTACCTGG[A/G]TTGTGGTGGTGATTA | 51366 |
rs746494935 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102332330 | TGTTGCTTTCTCCCA[C/T]CATGCCAGTAATGTT | 51366 |
rs746524839 | snp | C/T | 1.66073e-05 | 0.00288156 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295295 | CAAGCTGGGCAAATC[C/T]TGGAGGCTCTAAATC | 51366 |
rs746528567 | snp | A/C | 2.34321e-05 | 0.00342279 | intron-variant | UBR5 | GRCh38.p7 | 8:102361543 | TTCTTAATAAAGAAA[A/C]ATTGTTGTCAGAAGA | 51366 |
rs746528769 | snp | C/T | 5.22098e-05 | 0.00510903 | intron-variant | UBR5 | GRCh38.p7 | 8:102299591 | TATCATTATAGGCAA[C/T]ATATTCCTAACATGT | 51366 |
rs746537351 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102344654 | GCATTTTAGGCTGGG[C/T]GCAGTGACTCATGCT | 51366 |
rs746538881 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102331275 | CTTCATAGTTCAAGG[A/G]TCAGCTGGATAAAGT | 51366 |
rs746540987 | in-del | -/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102308977 | GAAAACTCTGCCCCT[-/C]CCCCCCCAAAAAACC | 51366 |
rs746552147 | snp | A/G | 1.75971e-05 | 0.00296618 | intron-variant | UBR5 | GRCh38.p7 | 8:102361675 | AGATCTTTTGTAAAC[A/G]AATACTTCTGACAGG | 51366 |
rs746564867 | snp | G/T | 1.72216e-05 | 0.00293437 | intron-variant | UBR5 | GRCh38.p7 | 8:102277238 | TGAAGGGAAAAAAAC[G/T]AATTAGATTTTGTCC | 51366 |
rs746565244 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102295915 | AATGCAAAGTATAAC[C/T]GTCAAAGCTTATATA | 51366 |
rs746573784 | snp | A/G | 1.64792e-05 | 0.00287042 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102342603 | AATGAGGCTCCATCA[A/G]GCCACCTTCGTTCAC | 51366 |
rs746577138 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102375972 | TAATTGGATATAAAC[A/G]TACACATTAAATTGT | 51366 |
rs746597065 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102351276 | ACAATTGCCAAGTGG[C/T]AGAAGCTACCCAAAT | 51366 |
rs746598252 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102372437 | CTTGAATCATAGTTT[G/T]TAAGGAGGACTTACA | 51366 |
rs746614877 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102255166 | CTTTTTAACTTAACC[A/G]AGGATATGCCTCCCT | 51366 |
rs746615784 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102364536 | TATCAATGGAAGATA[C/T]ATACGTAATGTTTAC | 51366 |
rs746646283 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102405567 | GGCTCCCGCCTGTAA[C/T]CCCAACACTTTGGGA | 51366 |
rs746647902 | snp | A/T | 1.64991e-05 | 0.00287215 | intron-variant | UBR5 | GRCh38.p7 | 8:102295387 | ATATTGCTTCCCACA[A/T]GTGTCATAAATGTCT | 51366 |
rs746651944 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102393302 | CTTAAATTTTACTCC[A/T]ATTTTTTTACAAGTT | 51366 |
rs746654796 | snp | C/T | 1.64876e-05 | 0.00287116 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102278908 | AGACCCTGACTTGGA[C/T]GGCCAAAAAGATCCT | 51366 |
rs746659903 | in-del | -/GCTGCA | | | cds-indel, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285700 | GCTTCCAAAGCAGCT[-/GCTGCA]GCTGCAGCACTTGTA | 51366 |
rs746666310 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102268139 | ATGGCATGGTCTTGG[C/T]TCACTGCAAGCTCCA | 51366 |
rs746667859 | snp | G/T | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102268986 | ACATTACCGTCCATG[G/T]GCAATAATGAGTTCC | 51366 |
rs746674734 | snp | C/G/T | 3.29491e-05 | 0.00405877 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102288230 | CCTGTTCATCATGAT[C/G/T]ATCCTCTTCTCCAGC | 51366 |
rs746680537 | in-del | -/T | 0.000175488 | 0.00936553 | intron-variant | UBR5 | GRCh38.p7 | 8:102265061 | TCATAAATTGAAATG[-/T]TTTTAAAAAATTCAA | 51366 |
rs746688239 | snp | A/G | 1.90998e-05 | 0.00309023 | intron-variant | UBR5 | GRCh38.p7 | 8:102257728 | TTCTCCTAAGAATGA[A/G]GAATGTAAATAAAAT | 51366 |
rs746688969 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102313955 | GTACCAAAAAGAAAA[C/T]GTAAAAGAGACTTTA | 51366 |
rs746706666 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102403772 | CAACCTCCACCTTCC[A/C]AGGTCAAGCAATGAA | 51366 |
rs746738742 | snp | A/G | 1.72024e-05 | 0.00293273 | intron-variant | UBR5 | GRCh38.p7 | 8:102323300 | ACGATTAGTTAAGCT[A/G]TAGTACTTACTTAGC | 51366 |
rs746740491 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102289657 | ATTTAACTCATTTAT[G/T]ACATGTGAGACACTT | 51366 |
rs746740928 | snp | C/T | 9.98021e-05 | 0.00706336 | intron-variant | UBR5 | GRCh38.p7 | 8:102311273 | TTGTGAATTAAAATG[C/T]CCAGTAGTTTCAATA | 51366 |
rs746742370 | snp | C/G | 1.82178e-05 | 0.00301804 | intron-variant, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102258957 | TCTATATAGTTCATT[C/G]TTTAAACATTTTTTT | 51366 |
rs746757644 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102304336 | AACACTTCAGACAGA[C/T]TGAACTATCTGATCT | 51366 |
rs746761107 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102324630 | GGCTTATAATTAAAT[A/G]TAAGAAACAAAAGAA | 51366 |
rs746774577 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102256395 | CCAATCCTTTCTGTT[C/T]TTGGTGGTTCTTACA | 51366 |
rs746814457 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102326244 | TTGTTAAACACAACG[A/T]TGCCTGGCCCTACCA | 51366 |
rs746827226 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102352218 | GGGGACTGAGGCAGG[A/G]GAATCACTTGAACCC | 51366 |
rs746832275 | snp | C/T | 4.94833e-05 | 0.00497385 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102281472 | TAATTTAGGAAGTCT[C/T]CTCGTGCAGACATCA | 51366 |
rs746842131 | snp | A/T | 3.2963e-05 | 0.00405961 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102360124 | ACCTGAGAGAAACCA[A/T]GGAGAGTCGCTTGTC | 51366 |
rs746846191 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102393967 | CTAGAGGAAAAAATA[C/T]TTTAGGTGAAACTAA | 51366 |
rs746846273 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102386588 | TTTTTAAAAAATTAA[C/T]GTAGACAAAAGGTAA | 51366 |
rs746849655 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102362862 | AGTAACTGAAATAAC[-/T]TTTTTTTTTTTTTGA | 51366 |
rs746860981 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102371410 | CCACCATGGCCAGCA[C/T]TGGATATTCTCTGAT | 51366 |
rs746920699 | snp | C/T | 1.65759e-05 | 0.00287883 | intron-variant | UBR5 | GRCh38.p7 | 8:102311523 | GGAAAATGGTAAAGT[C/T]TGACTCCTAATCAAA | 51366 |
rs746940930 | snp | A/C | 1.65274e-05 | 0.00287462 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102275599 | TTCTTTTACCTCAAA[A/C]CCACCCAATTCAGTT | 51366 |
rs746964408 | snp | C/T | 6.97143e-05 | 0.00590358 | intron-variant | UBR5 | GRCh38.p7 | 8:102285083 | TGTAAGTTGAGGATC[C/T]ATTTTAAGTTGGGGA | 51366 |
rs746967933 | snp | A/G | 1.65037e-05 | 0.00287256 | intron-variant | UBR5 | GRCh38.p7 | 8:102360201 | TTGACCTGGGGGAAA[A/G]CAAGAGGTAAATTTT | 51366 |
rs746978498 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102382767 | ACAGCCAAGAACCAC[A/T]GATACATGAGCAGAG | 51366 |
rs746984468 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102327158 | TCTGGCCTTGGCCTC[C/T]GAAAGTGCTGGGCCT | 51366 |
rs746989869 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102396715 | ATATATATATATTTT[-/T]TTTTTTCTTGAGACA | 51366 |
rs747006263 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102290759 | GGAATTTAAGACCGA[C/T]CTGGGCAACACAGCG | 51366 |
rs747016306 | snp | A/G | 1.73655e-05 | 0.0029466 | intron-variant | UBR5 | GRCh38.p7 | 8:102298375 | ATGTAACTCATTTAG[A/G]ATCTGAAATAAATTA | 51366 |
rs747021074 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102310301 | ACTTTGTTTCTAACC[C/T]GGATTATTGCCTGAC | 51366 |
rs747027242 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102364307 | CCGCCTTAGCCTCCT[A/G]AGTAAACAGAACTAC | 51366 |
rs747029203 | snp | C/T | 3.29527e-05 | 0.00405898 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102329155 | GGACTATCTTTTCAT[C/T]GGTTAACCCCAAAAA | 51366 |
rs747030626 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102264258 | TCTACTCTGCTATGC[C/T]ATCTCCCCATAGTCT | 51366 |
rs747045456 | snp | A/G | 1.67142e-05 | 0.00289081 | intron-variant | UBR5 | GRCh38.p7 | 8:102264605 | ATAATTCTAGAATAC[A/G]TATATCCCCCCACAC | 51366 |
rs747059482 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102346568 | GACCAGCCTGGCTAA[A/C]ATGGTGAAACCCCGT | 51366 |
rs747059499 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102278520 | AAGTTGTAGCCAAAA[G/T]TACACATGCTCATCT | 51366 |
rs747068582 | in-del | -/G | 1.65949e-05 | 0.00288048 | intron-variant | UBR5 | GRCh38.p7 | 8:102293944 | AACCAAAATCAAAAA[-/G]GATGCCTTACTTTTT | 51366 |
rs747082868 | snp | C/T | 1.65121e-05 | 0.00287329 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102294028 | AACGTAGAAACCTCA[C/T]TGTCACAGCAATAGC | 51366 |
rs747113267 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102327901 | CATGTAGCAACCTAA[A/G]GAATAAAATATTAGA | 51366 |
rs747113406 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102309261 | GGTTTCGCTATGTTG[C/T]CCAGGCTGGCCTCAA | 51366 |
rs747114059 | snp | A/G | 1.64942e-05 | 0.00287173 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102312385 | CAATCCTGCAGGAGA[A/G]AAGAAGGGTCAGCAT | 51366 |
rs747118437 | snp | A/C | 1.84439e-05 | 0.00303671 | intron-variant | UBR5 | GRCh38.p7 | 8:102294121 | TATCTAAAAGCTTTA[A/C]AAAATTATATTCACT | 51366 |
rs747122313 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102357771 | GAAGCTGGGTGCAAC[A/G]TACACATAAATTATT | 51366 |
rs747124638 | in-del | -/CAAAAAAAA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102386974 | AGCAAGACTCCGTCT[-/CAAAAAAAA]AAAAAAAAAAGACCT | 51366 |
rs747125139 | in-del | -/ACAA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102395488 | CAAACATACATACAC[-/ACAA]ACAAACAGTGTGTGT | 51366 |
rs747132677 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102390949 | ATATCGAGGCTGGGT[A/G]TGGTGGCTCACCCCT | 51366 |
rs747150187 | snp | C/T | 1.74227e-05 | 0.00295145 | intron-variant | UBR5 | GRCh38.p7 | 8:102286351 | GCAATACTAAGTTTT[C/T]AGACTTGCCTGCTGG | 51366 |
rs747175313 | in-del | -/AATAG | 0.000133078 | 0.00815607 | splice-acceptor-variant | UBR5 | GRCh38.p7 | 8:102281521 | CAAGGTGGCACGTCT[-/AATAG]ATAAGAACAGAAAGG | 51366 |
rs747181318 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102373080 | ACTCCTGGGCTCAAG[C/G]TGTCCTCCCACCTCT | 51366 |
rs747188192 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102378123 | GTCAAACAAATGTCA[A/T]CAAAATTAAAAAAAA | 51366 |
rs747193618 | snp | A/G | | | intron-variant, downstream-variant-500B, nc-transcript-variant | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102251873 | CTGAATCAGAAAGGA[A/G]GCAAGAGGATGAGGA | 51366 |
rs747198358 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102347702 | GGGTTGCAGTAGCAC[A/G]ATCTCGGCTCACTGC | 51366 |
rs747205256 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102342216 | TCTAGAACTAACATC[C/T]TAATTTCTCTGATTT | 51366 |
rs747220235 | snp | C/T | 1.66932e-05 | 0.002889 | intron-variant | UBR5 | GRCh38.p7 | 8:102312514 | CAAATTCAATGAACA[C/T]TAGCAATAGCTTATA | 51366 |
rs747220842 | snp | A/G | 1.65872e-05 | 0.00287981 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102265115 | CTGCCAATGTTTCTG[A/G]AACAATTCAACCTTG | 51366 |
rs747254431 | snp | A/T | 8.36995e-05 | 0.0064686 | intron-variant | UBR5 | GRCh38.p7 | 8:102279224 | CTAAACATAAAAAGA[A/T]AAAATGTTTTGTTTT | 51366 |
rs747255920 | in-del | -/GT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102304960 | TTACCTTCTGAGAAA[-/GT]GTAAAAAAAAAAAAA | 51366 |
rs747290084 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102408052 | TTGTGTGTGGAGGGT[A/G]CAAAATCACACCAAG | 51366 |
rs747340122 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102367457 | CCCCACTCCAGCCCC[A/G]CCCCCAGCAAACTGA | 51366 |
rs747350826 | in-del | -/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102315371 | CAGGATTAAAAAACT[-/G]AGCCCTCTTTAATGA | 51366 |
rs747360102 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102270668 | GGGATTACAGGCATG[C/T]GCCACCACACCTGGC | 51366 |
rs747370302 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102335870 | CAGATATGCATGATT[C/T]CATCTCCTCTGGGTA | 51366 |
rs747371973 | in-del | -/AAATC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102281261 | AAGCAAGTATTTCTT[-/AAATC]AACCTCATGGCAAGA | 51366 |
rs747382425 | snp | C/T | 1.65318e-05 | 0.002875 | intron-variant | UBR5 | GRCh38.p7 | 8:102295598 | TGTGCTGCGCTCTTT[C/T]GATTTAACTTACTGT | 51366 |
rs747388319 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102379080 | ATCACTTGCTAGTTA[C/T]AGAGATACATCTCAA | 51366 |
rs747417308 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102381172 | GGAGTTCAAGACCAG[C/G]CTGGTCAACATGGTG | 51366 |
rs747417646 | snp | C/T | 1.65241e-05 | 0.00287433 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102280460 | CCAGTTCCAAGAGTT[C/T]TCGCGTCCTTTAAAA | 51366 |
rs747442774 | snp | A/G | 1.75348e-05 | 0.00296093 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102271158 | TCCCTCCGAGAACCT[A/G]CTCGCAAACCACTAC | 51366 |
rs747459723 | snp | C/T | 1.64792e-05 | 0.00287042 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102272550 | GGGTGCCTTTGTTGG[C/T]ATTTTGGATACACTC | 51366 |
rs747461430 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102354210 | TCCAGATTTGCAGGT[C/T]TTCTTGGGACAAAAT | 51366 |
rs747462315 | snp | G/T | 1.6537e-05 | 0.00287545 | intron-variant | UBR5 | GRCh38.p7 | 8:102289602 | TCAGAAGCTTATGAG[G/T]GGGCTCCTGCCACAG | 51366 |
rs747476061 | snp | C/T | 1.65198e-05 | 0.00287395 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102261195 | TGTTCTGCGTATTTC[C/T]GCACATACTCATATA | 51366 |
rs747478173 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102395399 | ATATCTATTTATATA[C/T]ATACACACACACACA | 51366 |
rs747494148 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102330308 | TTTCTGGTTTTTCTG[A/T]CAAAATTCAATTTTA | 51366 |
rs747503347 | snp | A/G | 3.32862e-05 | 0.00407946 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295758 | CCAACAATCACAGTA[A/G]GCTGTTGGTGATGTC | 51366 |
rs747518921 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102305808 | CAGGCTGTAGTGCGG[C/T]GATGTGAACACAGCT | 51366 |
rs747540496 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102397024 | TCTCATTTTTAAGTA[C/T]CTCTGTGAGAACAGC | 51366 |
rs747552125 | snp | C/G | 1.656e-05 | 0.00287745 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102293615 | TTTACCTGCTAGACT[C/G]ATCAGATGATGGTCG | 51366 |
rs747560000 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102286028 | ACACATTTGGCAGTA[C/T]CTACAGACATTCTTG | 51366 |
rs747566171 | snp | C/T | 6.59544e-05 | 0.0057422 | intron-variant | UBR5 | GRCh38.p7 | 8:102295405 | GTCATAAATGTCTAA[C/T]TAACTCACCTTCAGG | 51366 |
rs747590562 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102366104 | AAAGACAGAAAGGTA[C/T]TTCTGACATCACATA | 51366 |
rs747641851 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102352307 | GAGTGAGACTCTGTC[G/T]CCAACAACAACAACA | 51366 |
rs747648900 | snp | C/G | 1.6863e-05 | 0.00290365 | intron-variant | UBR5 | GRCh38.p7 | 8:102300167 | CTAAAAGAACATGAA[C/G]AAAATCAGAGCTCAC | 51366 |
rs747671394 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102269470 | AAAAAAGAAGGGGGT[A/G]GGGTAGAGAAAAATA | 51366 |
rs747690263 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102382928 | ATAATTTTCCTGCAT[A/G]TAACTTCTAGTTAAG | 51366 |
rs747701348 | snp | C/T | 1.64955e-05 | 0.00287184 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295507 | TTGCGACTGTCTGTA[C/T]TAAGAATAGTAAGAG | 51366 |
rs747724634 | snp | C/G | 1.70078e-05 | 0.0029161 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102323490 | AGGATTATTTCTCAA[C/G]CATACCTAGCAAACA | 51366 |
rs747738735 | snp | C/G | | | intron-variant, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102258633 | GAGTTTAAGCAACAT[C/G]AATCAGAAAAGCCCA | 51366 |
rs747752326 | snp | C/T | 1.65578e-05 | 0.00287726 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102323347 | GCTTTTTCCATGTTT[C/T]TCAAGCTTTCAGGAG | 51366 |
rs747762004 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102338632 | GCTCTTTGCACTTTA[A/C]ATAAACTAACTTATT | 51366 |
rs747762498 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102364822 | ATTTAAGAAGTATTT[C/G]ATTATCTTTTACATT | 51366 |
rs747763908 | snp | C/T | 0.000115726 | 0.00760591 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102259122 | TCTAGTAGACCTTTC[C/T]TCATTGCCTAGAGAA | 51366 |
rs747764123 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102353000 | CCTGACTGTTACCAT[A/G]GAGAATACAGGTATT | 51366 |
rs747764713 | in-del | -/TTAGTTTACAGCCTAATATT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102378778 | TTTTAGTTTACTGAC[-/TTAGTTTACAGCCTAATATT]TTAGTTTACAGACTA | 51366 |
rs747784866 | snp | A/T | 1.65875e-05 | 0.00287984 | intron-variant | UBR5 | GRCh38.p7 | 8:102271110 | TCCAAAAAGGTGGTA[A/T]TGAATCAAAGATACA | 51366 |
rs747801639 | snp | C/T | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311436 | CCCTTATTCCTCCCA[C/T]GCAATCTTTGGCCAT | 51366 |
rs747811915 | snp | C/G | | | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102326583 | GGCATTGAAGAAATA[C/G]CAGCACTGGATTTAG | 51366 |
rs747820730 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102270388 | AATTTTTATTGTAAG[A/G]GAGTAGGACCTTAAC | 51366 |
rs747847373 | snp | C/T | 1.66466e-05 | 0.00288496 | intron-variant | UBR5 | GRCh38.p7 | 8:102311535 | AGTTTGACTCCTAAT[C/T]AAAAAATGTATCTGA | 51366 |
rs747857509 | snp | C/G | | | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102329354 | TACTGCTGACAGCCA[C/G]AAGTTCAGAATACAG | 51366 |
rs747894298 | snp | A/G | 1.65282e-05 | 0.00287469 | intron-variant | UBR5 | GRCh38.p7 | 8:102360221 | AGGTAAATTTTTGAA[A/G]ACCAACATTTTTTAC | 51366 |
rs747911400 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102298201 | GCTGTTTTTTGATGG[A/G]AAGTTGGAAGATACA | 51366 |
rs747920312 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102292687 | TATTTAATCATGGGA[C/T]AGATTTGACAAGTCT | 51366 |
rs747942169 | snp | C/T | 1.65647e-05 | 0.00287786 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102275806 | CATGGGAAATAACCA[C/T]TCCCATAAAGCTACA | 51366 |
rs747942797 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102341181 | CCTGCAAATATGAAA[C/T]AGACACAACTCTAAC | 51366 |
rs747961014 | in-del | -/ACAC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102382828 | AAATCACATTAAAAC[-/ACAC]ACACACACACACACA | 51366 |
rs747968911 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102300577 | AAACCAGTATTGTTC[-/A]AACACTAAATCCCTT | 51366 |
rs747971177 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102276026 | ATTTTTCCTCCCTTA[G/T]TCCTTCTGTATTCTA | 51366 |
rs747982538 | snp | A/C | 1.64895e-05 | 0.00287132 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102329195 | TGGATGATGTAATGA[A/C]GGATTCTTTGAAAGC | 51366 |
rs747984717 | snp | A/G | 3.30235e-05 | 0.00406333 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285166 | CTAGCTTCTTCTCGC[A/G]CAGTCATCCTCTCTC | 51366 |
rs748010464 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102305571 | CTCTGCAACTGAAAC[A/T]GGAAAGCAGCCACAT | 51366 |
rs748026704 | snp | C/T | 1.64947e-05 | 0.00287177 | intron-variant | UBR5 | GRCh38.p7 | 8:102360583 | AGAAAGGACATAATA[C/T]CTTACCCATCATTAT | 51366 |
rs748029605 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102360014 | AGACTGAGAGCACTC[A/C]CAGGAAGATGATACA | 51366 |
rs748048109 | in-del | -/AAAG | | | intron-variant | UBR5 | GRCh38.p7 | 8:102365484 | AAAAAAAAAAAACAC[-/AAAG]AAAGAAAATAACCTC | 51366 |
rs748077168 | snp | C/T | 1.65211e-05 | 0.00287407 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102329373 | TTCAGAATACAGAGC[C/T]CCAATACAGATGAAT | 51366 |
rs748079409 | snp | A/G | 1.6599e-05 | 0.00288084 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102298874 | AAGTTCTCGTAGATA[A/G]GGCTGGAGAACCACA | 51366 |
rs748081383 | snp | C/T | 3.9e-05 | 0.00441571 | intron-variant | UBR5 | GRCh38.p7 | 8:102294129 | AGCTTTAAAAAATTA[C/T]ATTCACTCTATTAAT | 51366 |
rs748083826 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102402524 | GTCTGGGCTTTCTTA[A/G]CTTTCTCCATCAAAT | 51366 |
rs748093789 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102389500 | ATAGAGTAAGAACCA[C/T]CTACCAAGTACTGTC | 51366 |
rs748099878 | snp | C/T | | | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102278936 | CCTCCTTTCTAGCAT[C/T]TGGCTGGAATTTTAA | 51366 |
rs748108616 | snp | A/G | 3.4188e-05 | 0.00413435 | intron-variant | UBR5 | GRCh38.p7 | 8:102275877 | GAAATAATTTAGCCA[A/G]TTTCAAAGACTGATT | 51366 |
rs748127153 | snp | A/G | 1.64833e-05 | 0.00287078 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102265183 | TCTTTTCCCAGGTTG[A/G]TAAAACAAAGGGGCA | 51366 |
rs748147186 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102280338 | AAAAAGCTTGAAGGG[G/T]AACTACTGAGGCAGC | 51366 |
rs748151552 | snp | C/T | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102286523 | AAAGGTCTCCTGTTC[C/T]ATGTCGTCACTCTGA | 51366 |
rs748162515 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102299263 | TACAAATCTCATCTG[A/G]TTTCTAAATGTATGT | 51366 |
rs748162634 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102335180 | AAAACATATTGTGTG[A/G]TCTCACTTATATGTG | 51366 |
rs748163714 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102310378 | TTGAGACGGAGTCAC[A/G]CTCTGTTGCCCGGGC | 51366 |
rs748166612 | snp | A/G | 1.65985e-05 | 0.00288079 | intron-variant | UBR5 | GRCh38.p7 | 8:102313762 | ATAACCAATATCATT[A/G]TAATTCTGTTAGTAA | 51366 |
rs748171667 | in-del | -/A | 1.67323e-05 | 0.00289239 | intron-variant | UBR5 | GRCh38.p7 | 8:102269990 | CTTTAATTCAAAAGC[-/A]AAAAAATAACACAGC | 51366 |
rs748183266 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102347863 | AGGTGATCCACCCAC[C/T]GTGGCCTCCCAAAGC | 51366 |
rs748201775 | snp | A/G | 3.29473e-05 | 0.00405864 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311416 | AAGATCCAGCCAATC[A/G]GGATCCCTTATTCCT | 51366 |
rs748202292 | snp | C/T | 1.65395e-05 | 0.00287567 | intron-variant | UBR5 | GRCh38.p7 | 8:102295124 | AGACTTGAGGAGAAA[C/T]GAAAGACAGAATGAA | 51366 |
rs748206443 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102266917 | ATTTAAATTCTGTGA[C/T]TATCAGCACATGAAT | 51366 |
rs748230273 | snp | A/G | 2.06832e-05 | 0.00321577 | intron-variant | UBR5 | GRCh38.p7 | 8:102286638 | ATTTTTATTTTTAAA[A/G]CCAAAAACATTGTGA | 51366 |
rs748231761 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102361693 | TACTTCTGACAGGTA[C/T]TTGTACCATTATTTT | 51366 |
rs748247451 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102349038 | TATGCAGTATCTGTA[C/T]CTATAGCCTAAGAAC | 51366 |
rs748248735 | snp | C/T | 6.61255e-05 | 0.00574964 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102280464 | TTCCAAGAGTTCTCG[C/T]GTCCTTTAAAAAGAC | 51366 |
rs748262789 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102379933 | TGGGTGCCAGAGCTG[A/G]GTTCATCCTAGAAGC | 51366 |
rs748274148 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102371544 | GTCTAATCCTGTACT[C/T]TGAGTACACTGTTTG | 51366 |
rs748288082 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102391038 | GATCAGCCTAGGCAC[C/T]ATAGTGAGACCCCAC | 51366 |
rs748289189 | snp | A/T | 1.69347e-05 | 0.00290982 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102304199 | AAAATTAAGATCAAT[A/T]TAAGTTTTAGAACTA | 51366 |
rs748291328 | snp | C/T | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102313850 | ACAAAAACCACTTCC[C/T]GAAGAGACCACTGCT | 51366 |
rs748293735 | snp | A/C | 1.65381e-05 | 0.00287555 | intron-variant | UBR5 | GRCh38.p7 | 8:102295614 | GATTTAACTTACTGT[A/C]TGTTCTAAAAATCCC | 51366 |
rs748324812 | in-del | -/AAT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102367982 | TTGAATTAGACACTC[-/AAT]AATTTTCAGACACAT | 51366 |
rs748347717 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102367512 | CAAAGGGTATCCCAA[A/C]CCCAAATCCCTTTTC | 51366 |
rs748359901 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102272129 | CTCACTGGGGACCAG[A/G]AGCAAGTTTGGAAAT | 51366 |
rs748361831 | snp | A/G | 1.64928e-05 | 0.00287161 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102254398 | GTAAAGTCGAGAAAT[A/G]CAAGTATTTGCAGTA | 51366 |
rs748366779 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102409107 | AAAGGAGATCAAAAT[A/G]TCCAAAGTATCTGAG | 51366 |
rs748379129 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102285858 | ATTATATATACTTAC[A/G]TAAATCTAAATGGTC | 51366 |
rs748383661 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102393265 | TGAAAATTCTGGTCA[A/G]TTTACTAGGGGAAAA | 51366 |
rs748402431 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102391789 | AAGGCTGAGACCTAC[G/T]AGGTCGTGTTCCCAG | 51366 |
rs748406725 | snp | C/T | 1.70834e-05 | 0.00292257 | intron-variant | UBR5 | GRCh38.p7 | 8:102346896 | AAGTGTTCTACGAGA[C/T]CCATACCTGTGAAAT | 51366 |
rs748410793 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102279760 | ACCTTGTTTGCGTAT[-/A]AACGGCAGTGAGCTA | 51366 |
rs748421183 | snp | C/T | 3.30857e-05 | 0.00406716 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102281295 | AATGGATACCTTTTG[C/T]GTTCTAGTTGAGGTG | 51366 |
rs748435750 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102379210 | CTCATCTCCAGCCAG[A/G]TGCTCTTTGTAACTG | 51366 |
rs748455413 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102306884 | TACATCTGTCAGTTA[C/T]TCTTATAGCAAAAGG | 51366 |
rs748469481 | snp | C/T | 1.6902e-05 | 0.00290701 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102296968 | AGCAAGCCACAAGTT[C/T]GACACTCAAAAATAT | 51366 |
rs748474467 | snp | C/T | 1.64977e-05 | 0.00287203 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102326604 | CTGGATTTAGGCTTT[C/T]TATTTTTTGCTCTAG | 51366 |
rs748480205 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102383538 | GAAACCAGCCCAACA[A/G]GAAAAATATATATAT | 51366 |
rs748486074 | snp | G/T | 3.29636e-05 | 0.00405964 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311484 | TTCCATCTCGAAGAA[G/T]AATGGGAGATTCCTA | 51366 |
rs748528614 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102368625 | GAGACGAGTGGGGTG[A/G]GTGAGGGTAGGGGGG | 51366 |
rs748550914 | snp | A/C | 1.64893e-05 | 0.0028713 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102272714 | GCACATCTTCGACCA[A/C]AGTGATTGTTAAGCT | 51366 |
rs748562954 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102410319 | AAGTTAGGACTAATA[C/T]AGAAAACATGCCCTA | 51366 |
rs748567709 | snp | A/G | 0.000294538 | 0.0121319 | intron-variant | UBR5 | GRCh38.p7 | 8:102312111 | ATATAGGATATGCCA[A/G]CTGAAGAAGTTTCAA | 51366 |
rs748607404 | snp | G/T | 1.65165e-05 | 0.00287367 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102293628 | CTGATCAGATGATGG[G/T]CGTGGTGGTAGTGGT | 51366 |
rs748612539 | snp | C/T | 1.65729e-05 | 0.00287857 | intron-variant | UBR5 | GRCh38.p7 | 8:102361108 | TTCATTTCTGTATCT[C/T]AGAGTGAATAATTTA | 51366 |
rs748621793 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102386453 | AAAAAGAAAAATGAG[C/T]ACGGAGACTGTCACT | 51366 |
rs748624610 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102385781 | TCTGATACTGCTATT[C/G]TACCTTTTACATTTC | 51366 |
rs748627611 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102262295 | TTATATTTTGAAAAA[A/C]TATAAAGCCAAAAGC | 51366 |
rs748648498 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102356184 | GCCAGGCGCGGTGGC[G/T]GACACCTGTAATCCT | 51366 |
rs748657497 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102294801 | GAGGGCACTGATAGT[C/T]TTATGTTTTCCAGAG | 51366 |
rs748662672 | in-del | -/TTG | 1.64852e-05 | 0.00287094 | cds-indel, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102329091 | AAAGTGTTTCATACC[-/TTG]TTATTTTCTGTAGCT | 51366 |
rs748669794 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102261064 | CCTTTTATAAATAAG[C/G]TGAATATACTTAGCT | 51366 |
rs748669895 | in-del | -/A | 1.66832e-05 | 0.00288814 | intron-variant | UBR5 | GRCh38.p7 | 8:102305341 | TCAATGAATTTGAGT[-/A]AGCACATTACATATA | 51366 |
rs748714585 | snp | C/T | 0.00016592 | 0.00910673 | intron-variant | UBR5 | GRCh38.p7 | 8:102289425 | TCATAAAATAAAAGC[C/T]TTTTAAATCTACCAC | 51366 |
rs748732387 | snp | A/T | 1.80312e-05 | 0.00300254 | intron-variant | UBR5 | GRCh38.p7 | 8:102323537 | AAGATGACATAACTT[A/T]AAAAATATATATAAT | 51366 |
rs748764223 | snp | A/T | 1.67158e-05 | 0.00289096 | intron-variant | UBR5 | GRCh38.p7 | 8:102259150 | GAATTTCAGAAACAA[A/T]AATACTTCATTTTCC | 51366 |
rs748776596 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102271619 | TTAGTTTTTGGCATG[A/G]AAGCATTAAAGGCCA | 51366 |
rs748803821 | snp | A/C | | | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102259037 | TTGCACATTGACTTC[A/C]CCGCAGCCATTTACC | 51366 |
rs748844038 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102395293 | CTTTTTCATGAACCA[A/C]ACACCACCACCAGAC | 51366 |
rs748856503 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102316364 | GAAAAAAAGAAAATA[A/C]ATTGATGTGTTAAAT | 51366 |
rs748856904 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102265937 | TTGTCCCACAGGTCT[C/T]CCTGAAACTGTCCTT | 51366 |
rs748861764 | snp | C/T | 1.65061e-05 | 0.00287277 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311845 | TAGCAAGATCAAAGA[C/T]ACAGTATCGTACCCA | 51366 |
rs748887296 | snp | C/T | 1.648e-05 | 0.0028705 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102289568 | TAGGATGACTGAGAC[C/T]GACTGGAGCTGTAAA | 51366 |
rs748891281 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102410599 | TTTTCAGTAAGTATT[G/T]CAAAAGATTCCCAAA | 51366 |
rs748906401 | in-del | -/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102332233 | CTTCTCTTTCTCTCT[-/C]CCCATACCCCTGCTT | 51366 |
rs748908320 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102294140 | ATTATATTCACTCTA[C/T]TAATGTTAAGATACT | 51366 |
rs748911439 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102341378 | GGCAGTTGCCAAAGA[A/G]AACAGAATAACCTTT | 51366 |
rs748927451 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102383929 | GAATCAAAACAGCAC[C/T]GAACTCCTCAAAAGG | 51366 |
rs748929627 | snp | G/T | 4.95757e-05 | 0.00497849 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102261185 | CAACATTCTGTGTTC[G/T]GCGTATTTCCGCACA | 51366 |
rs748944399 | snp | C/T | 1.66283e-05 | 0.00288338 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102298468 | TACAGCTGACATAAA[C/T]GGGGTCATCCCTCTT | 51366 |
rs748959412 | snp | C/T | 1.67419e-05 | 0.00289321 | intron-variant, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102276933 | TATATATTTTTAACG[C/T]TGTACTGAACAATAA | 51366 |
rs748972605 | snp | G/T | 4.94556e-05 | 0.00497246 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102360625 | CCCAATTCCAATCTG[G/T]CTGGCTGTACTGAAA | 51366 |
rs748984520 | snp | A/G | | | missense, upstream-variant-2KB, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102304166 | CTTTCAGAACGCTCC[A/G]CTTCTGAAAAATGAG | 51366 |
rs748988568 | snp | A/T | 1.65512e-05 | 0.00287669 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102298904 | ACTGTCACATAACAA[A/T]TTCAATATAAAATGA | 51366 |
rs748998356 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102293056 | GTTATAAAATCAGAC[C/T]TGAAAAAACAAAATA | 51366 |
rs748998787 | in-del | -/TT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102335202 | TTATATGTGAAGTCT[-/TT]TTTTTTTTTTAAAGG | 51366 |
rs749000798 | in-del | -/CTC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102292334 | ATTATCACATGAGAT[-/CTC]CTCCTTCTGGGAAGA | 51366 |
rs749020257 | in-del | -/TTT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102380721 | AAAATTTAACATGCT[-/TTT]TTTTTTTTTTTTTTT | 51366 |
rs749030127 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102366415 | AAAGACAGAATACAA[C/T]TTGCCAAGTCTTTCC | 51366 |
rs749037608 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102280509 | ACTTGAAGTATTTGT[A/G]TAATATGAACAGGAG | 51366 |
rs749049389 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102361902 | GAGAAAACTGAAGCT[C/T]CTAGAGTTTATAGAA | 51366 |
rs749065289 | in-del | -/AAACATA | | | splice-acceptor-variant | UBR5 | GRCh38.p7 | 8:102279210 | TTCAAAGTAGCACCT[-/AAACATA]AAACATAAAAAGATA | 51366 |
rs749066927 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102266016 | ATCTATCTTCAAGCT[A/G]ACTGACACTTTCCTC | 51366 |
rs749074232 | snp | C/G | 3.31389e-05 | 0.00407042 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102265253 | ACTACACTTCGACTA[C/G]AGCCATGGCGCTTTC | 51366 |
rs749088649 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102280787 | AAGGCAGGGGGATCA[C/T]TTAGGCCAGGAGTTG | 51366 |
rs749094531 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102330741 | TTCAGGTAAACTATA[C/T]AATTTCTCTGAAACC | 51366 |
rs749100029 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102343293 | TTTTTTTTAAAAATA[A/C]TCTTTATAAAATGAT | 51366 |
rs749102329 | snp | G/T | 1.65466e-05 | 0.00287628 | intron-variant | UBR5 | GRCh38.p7 | 8:102295137 | AACGAAAGACAGAAT[G/T]AACTGTAAAAGGTCT | 51366 |
rs749112668 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102329534 | ATACGAAGTCTTTAG[C/G]ACAGCCTACAAGGTA | 51366 |
rs749118528 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102391929 | ACCAAAATCGAGAGA[A/G]CAATGTAAGTGACCT | 51366 |
rs749124015 | snp | C/T | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102277089 | TTTGAACTCTCAGTT[C/T]CTTCTGGCAGCACGG | 51366 |
rs749154049 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102402724 | TTGTCTGTGAGGTAG[A/C]CCTGGTATCTGAATT | 51366 |
rs749158109 | snp | C/T | 6.66056e-05 | 0.00577047 | intron-variant | UBR5 | GRCh38.p7 | 8:102342438 | GTTGTCAGGGATCCA[C/T]TTAAATGGAAGCAGT | 51366 |
rs749164142 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102374617 | AAAAGAAAGCAGGTA[C/T]GTAGGTAGGTAGGTG | 51366 |
rs749165689 | in-del | -/AATT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102323097 | AGTATAATAATAATA[-/AATT]AATTAATTAATTAAT | 51366 |
rs749221438 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102389393 | GAGATGCCTAAGGAA[C/T]CCCAGCTGTTGCAGA | 51366 |
rs749226522 | snp | A/G | 4.97591e-05 | 0.00498769 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295251 | CATAGATTTCAAGGC[A/G]TTCCAGTCCTGTAGA | 51366 |
rs749226931 | snp | A/C | 3.75143e-05 | 0.00433079 | utr-variant-3-prime, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102254291 | ACACAGCAATACACA[A/C]TTTTTATACTCTACA | 51366 |
rs749227017 | in-del | -/AACT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102344998 | CTAAATCCATTCTAG[-/AACT]TAAGTTTTTTCACAT | 51366 |
rs749249665 | snp | C/G | 6.59598e-05 | 0.00574243 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102254452 | TCTTATTGTGATTGA[C/G]GGCATAGGCTGGAAT | 51366 |
rs749249735 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102400678 | TGACCTTACAAGCAC[C/T]GAAATGCATTTTAAA | 51366 |
rs749269533 | snp | A/C | 1.67416e-05 | 0.00289318 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102287563 | CAGCTCCATATCACT[A/C]CCTAAAAAATACATT | 51366 |
rs749270416 | snp | C/T | 3.48475e-05 | 0.00417403 | intron-variant | UBR5 | GRCh38.p7 | 8:102314725 | ATTTTCACAAATGCA[C/T]ACAACAAATAAAACT | 51366 |
rs749272349 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102391086 | AAGTGGGAGAATCTC[G/T]TCAGCCTGGGAGGTT | 51366 |
rs749274917 | snp | C/T | 1.66263e-05 | 0.00288321 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102257667 | TGCTCATCTTCTCTA[C/T]TATTGACCAGAACCA | 51366 |
rs749276851 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102409231 | CAACATCCTCTTCTT[C/T]CCACCCCAGCCATCC | 51366 |
rs749280234 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102313726 | GAAGAAAGGACTCAG[A/G]TATCAACCACAAATC | 51366 |
rs749280614 | snp | C/T | 8.23676e-05 | 0.00641693 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102313889 | ACCTTTTCCTCTTCT[C/T]TTGGTGCAGGGGTTG | 51366 |
rs749296017 | in-del | -/T | 8.26986e-05 | 0.00642981 | intron-variant | UBR5 | GRCh38.p7 | 8:102279023 | AACCTTAAGACTAAC[-/T]TGTTTAATTCACCTG | 51366 |
rs749298615 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102299424 | TTTCTTCCAGATGAC[C/T]AGGCAGACAAAGAGT | 51366 |
rs749311963 | snp | A/G | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102305183 | CTGTGGCTGATGAAT[A/G]TCTGCAGCATCTGTA | 51366 |
rs749315274 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102267196 | CTTTAAAAAAGTGTA[C/T]CACTAGATCCTTCAT | 51366 |
rs749315803 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102323547 | AACTTTAAAAATATA[C/T]ATAATATTTATTTCA | 51366 |
rs749332221 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102336287 | TATGACATGCATGGT[C/T]TGCAAATATTTTTTC | 51366 |
rs749344583 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102318536 | TAATATCCAGGAGAA[A/C]TTCCCCAGTCTAGCA | 51366 |
rs749345136 | in-del | -/AA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102399947 | CAAGACTCTGTCTCA[-/AA]AAAAAAAAAAAAAAA | 51366 |
rs749361413 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102301051 | AGGGCCAGAAAACGC[A/C]TAAGGGACTTCATTC | 51366 |
rs749371630 | in-del | -/AAG | | | intron-variant | UBR5 | GRCh38.p7 | 8:102274083 | GTAGCAAAACCTACA[-/AAG]AAGAATTACTTCAAG | 51366 |
rs749372789 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102350938 | CCAACAAGCAAATGA[A/G]AAGATGTTTAACACC | 51366 |
rs749375389 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102337368 | ATATTATTGGAAAAG[C/T]TCTGAGTTGCTCCCT | 51366 |
rs749377820 | snp | C/T | 9.93509e-05 | 0.00704738 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102347070 | CTCCACCACTTCCAC[C/T]CACTCCAGAACTCCA | 51366 |
rs749440464 | snp | C/T | 5.21218e-05 | 0.00510472 | intron-variant | UBR5 | GRCh38.p7 | 8:102295807 | ATTTATACACAAGTA[C/T]AAAAACTGAAATTTT | 51366 |
rs749441766 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102380106 | AGAGGAAAAAAACAG[A/C]AAAGAGGCCGGGCGC | 51366 |
rs749462648 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102274286 | TGTCCTCGAATTCCT[G/T]GACTCAAACCATCCT | 51366 |
rs749475424 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102261403 | ATGGAAACATTTTAG[G/T]CCAAAAAAAGGACAA | 51366 |
rs749488274 | in-del | -/A/AA/AAA/AAAA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102255420 | TATATAAAGGGACAG[-/A/AA/AAA/AAAA]AAAAAAAAAAAAAAA | 51366 |
rs749493311 | snp | A/G/T | 3.7066e-05 | 0.00430487 | intron-variant | UBR5 | GRCh38.p7 | 8:102296998 | TCCTAAAATTAAGAG[A/G/T]GTACTTTTAAAGGAA | 51366 |
rs749497588 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102398185 | TACATTTACAGTGAA[C/T]TCATTTTCAACAAAG | 51366 |
rs749521982 | snp | C/T | 0.000116031 | 0.00761592 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102261947 | CTTTACACAGGTCAA[C/T]TGCAAATGCCAAATC | 51366 |
rs749530552 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102410745 | CACTGACACAAGAGG[C/T]CAGTATCTCAGCAGC | 51366 |
rs749530564 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102289374 | AGTAGTCTCAAGCTA[C/T]TATTAATGTAATTTC | 51366 |
rs749535092 | snp | C/G | 1.66782e-05 | 0.0028877 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102275530 | CTTTACCTCTAGTGA[C/G]AAATCTCTTGACTGC | 51366 |
rs749557077 | snp | A/G | 1.64895e-05 | 0.00287132 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102360090 | AGGTGTTGCCTGCCA[A/G]CCTGCCTAGAGTCTC | 51366 |
rs749567270 | in-del | -/AAG | 1.77148e-05 | 0.00297609 | intron-variant | UBR5 | GRCh38.p7 | 8:102327900 | CCATGTAGCAACCTA[-/AAG]AATAAAATATTAGAA | 51366 |
rs749586644 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102262568 | AGACTCAATATATCA[A/C]CAATTTTATGTTGCC | 51366 |
rs749594460 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102344878 | AGGCTGCAGTGAGCC[A/G]AGATCGTACTACTGC | 51366 |
rs749596380 | in-del | -/ATATCTCCATAATCATTT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102361352 | AATAATTGAAAAATA[-/ATATCTCCATAATCATTT]ATATCTCCCTGTATG | 51366 |
rs749599039 | snp | A/G | 1.64909e-05 | 0.00287144 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102327826 | TCTCCTTGAAGTTCA[A/G]AGTAAGTCTGAGCAG | 51366 |
rs749614542 | in-del | -/TCT | 1.64933e-05 | 0.00287165 | cds-indel, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102305087 | TTCTTAATCTCACCC[-/TCT]TCTTCTTTAGTTTCT | 51366 |
rs749695991 | snp | C/G | 2.29113e-05 | 0.00338455 | intron-variant | UBR5 | GRCh38.p7 | 8:102361554 | GAAAAATTGTTGTCA[C/G]AAGATTTAAATATTT | 51366 |
rs749696271 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102307848 | TTTCCTCCAACCCTG[G/T]GGATGTTCCTTCTCG | 51366 |
rs749730899 | snp | A/G | 3.32369e-05 | 0.00407644 | intron-variant | UBR5 | GRCh38.p7 | 8:102312252 | TTTGACAACCTGCAT[A/G]ACACAAAAGGAATTT | 51366 |
rs749731341 | snp | C/T | 1.71457e-05 | 0.0029279 | intron-variant | UBR5 | GRCh38.p7 | 8:102299977 | TTGTTAAACACTAAA[C/T]GAAATTAAATAACAG | 51366 |
rs749745413 | snp | C/T | 1.65732e-05 | 0.00287859 | intron-variant | UBR5 | GRCh38.p7 | 8:102278779 | ATATGCTGGGACAAG[C/T]TGTCCTTAATAAATG | 51366 |
rs749750885 | in-del | -/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102408316 | TTCAGAGATTGATGT[-/G]GGGGGGTTCTAAGAG | 51366 |
rs749754489 | in-del | -/A | 0.400402 | 0.202002 | intron-variant | UBR5 | GRCh38.p7 | 8:102275622 | TTCAGTTAGGATCTT[-/A]AAAAAAAAAAAAATG | 51366 |
rs749762559 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102283815 | TAATTTTCCTATTAG[A/T]TACTCAGGATCAAGG | 51366 |
rs749775419 | in-del | -/A | 1.65395e-05 | 0.00287567 | intron-variant | UBR5 | GRCh38.p7 | 8:102295621 | CTTACTGTATGTTCT[-/A]AAAATCCCACTTGCC | 51366 |
rs749791066 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102376265 | AATATGGCTCATCAT[A/C]GAAATCCCTGGGGAA | 51366 |
rs749804037 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102395814 | TTAAAAAGTTTCTCA[C/T]TGAGCATGTGGCAGT | 51366 |
rs749819339 | snp | A/G | 0.000114188 | 0.00755519 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102412131 | GGGAGGGAGGGAAGG[A/G]CGCCCCTCCCCCCGC | 51366 |
rs749827866 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102388030 | ACATGTGTAAAACAC[A/G]CGCTCTTTTTCACAT | 51366 |
rs749831305 | snp | C/T | 8.26986e-05 | 0.00642981 | intron-variant | UBR5 | GRCh38.p7 | 8:102278961 | TTTTAACAGAAATAT[C/T]CTAGTTACATTGAAT | 51366 |
rs749840912 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102307559 | AATGGAGGGTGAATA[C/T]GCTCCCATATTAAAC | 51366 |
rs749849072 | snp | C/T | 1.6549e-05 | 0.0028765 | intron-variant | UBR5 | GRCh38.p7 | 8:102360039 | GATACAGACCATCTG[C/T]AAGATGGTGCCTTCA | 51366 |
rs749867440 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102273970 | CTGCCACACTGTAGA[C/T]ATTTTACATTGATTA | 51366 |
rs749884232 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102385706 | ACAGGAACAAGCTAC[G/T]GCACCCAGCTAATCC | 51366 |
rs749893494 | snp | C/T | 1.94026e-05 | 0.00311463 | intron-variant | UBR5 | GRCh38.p7 | 8:102275477 | TAAAATTTATATAAA[C/T]AGCATACTACAGGTA | 51366 |
rs749911304 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102358028 | GCACGCGCCTATAGT[C/T]CCAGCTACTTGGGAG | 51366 |
rs749924167 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102355882 | CTTAAAATTAGCCCT[A/C]ATCTTCTTCAGAGTA | 51366 |
rs749940818 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102369777 | TCATCAAGGACACTT[G/T]GAAGTGAAACTGGCT | 51366 |
rs749947521 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303946 | AATGAAACAAAAAAG[A/G]ACCCACCAATTCATG | 51366 |
rs749962744 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102334614 | GTTAATTAACAGTAC[C/G]GAGTCAGGCGCCGTG | 51366 |
rs749972107 | snp | C/T | 1.65833e-05 | 0.00287948 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102297458 | GTAGAAATAACTTAC[C/T]TGGTTAATGTGCTCT | 51366 |
rs749973548 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102395161 | CAATCCCTATTCTCA[-/T]TTTCAACACTTCTTC | 51366 |
rs749984298 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102337853 | CAGACATTCAGCAAC[A/G]TATTATGAAATTTCT | 51366 |
rs749984594 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102270666 | CTGGGATTACAGGCA[G/T]GCGCCACCACACCTG | 51366 |
rs749990431 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102381822 | TTTAAGAAAAGATGG[-/T]TTTTAAATTTAAAAA | 51366 |
rs750005175 | snp | C/T | 3.37371e-05 | 0.00410699 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102293732 | GACGAGCAATCCCCA[C/T]TCTGACAGGAACAAT | 51366 |
rs750020851 | snp | G/T | 1.65321e-05 | 0.00287502 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102262030 | TGCCGCAAACTCTCA[G/T]ACATTACAGGATCAA | 51366 |
rs750025418 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102263319 | ACTTAAACCTGGGAG[A/G]TGGAGGTTGCGGTAA | 51366 |
rs750037716 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102387521 | GAGATCAGTCTGGGC[A/G]ACACAGTAAAACCCG | 51366 |
rs750039611 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102273288 | CTTAGAAAAATGGGC[A/G]TATCAACTGAGTTAA | 51366 |
rs750050987 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102296580 | GGACCTGAGACCTCC[A/G]CTGCATAATACACTC | 51366 |
rs750051161 | snp | A/C/T | 6.63288e-05 | 0.00575853 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102312218 | GGAAACAGTCGGGAA[A/C/T]CTTCGGTGTTCCACC | 51366 |
rs750055458 | in-del | -/CTAGTTAA | 1.6524e-05 | 0.00287432 | intron-variant | UBR5 | GRCh38.p7 | 8:102288301 | TGTAGACAATCAAAG[-/CTAGTTAA]CTAAAATGCGAAGAC | 51366 |
rs750055692 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102393705 | GAGGCTGAGGAAGGC[A/G]GATCACTTGAGGCCA | 51366 |
rs750099166 | snp | C/T | 3.32231e-05 | 0.00407559 | intron-variant | UBR5 | GRCh38.p7 | 8:102293923 | ACAGAGTGAAAATGG[C/T]ATCTAAACCAAAATC | 51366 |
rs750113577 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102398969 | AAAATGAGCAAAAGG[C/T]CTGAATAGACATTTC | 51366 |
rs750140654 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102297697 | GCCTTAGCATACACA[C/T]AATATAAACCAGAAA | 51366 |
rs750154514 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102308653 | AGGTCACTGATTTCT[A/G]AAGTATTTACTATAC | 51366 |
rs750156446 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102262178 | TAATTTGAAGATACA[C/T]TGATATAGAATAATT | 51366 |
rs750192454 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102283139 | AAACAAAATATAGTA[C/T]GCTCATACAATGAAA | 51366 |
rs750195414 | snp | A/G | 6.59435e-05 | 0.00574172 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102278901 | AGAATAAAGACCCTG[A/G]CTTGGACGGCCAAAA | 51366 |
rs750210323 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102345622 | AGAGCTCTAAAAATT[A/C]ACATACATTTAAAAA | 51366 |
rs750231418 | snp | G/T | 0.000214431 | 0.0103523 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102300068 | GAAACTGGATCCTGG[G/T]GGTCACTGGATGAAG | 51366 |
rs750251655 | snp | A/C/G/T | 0.000118585 | 0.00769944 | intron-variant | UBR5 | GRCh38.p7 | 8:102285390 | AATAGAGCTAAATTC[A/C/G/T]ATACAGCAGCAGTAT | 51366 |
rs750251761 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102311084 | TATATCTCTCCCCTT[G/T]GTGCTCCTACAACAT | 51366 |
rs750291719 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102374777 | AACTAGGCATTTCTC[C/T]GAATTCCAATATACC | 51366 |
rs750298429 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102377256 | TCTAGAACATAGAAA[A/C]CTCCTCCAAAAGGCA | 51366 |
rs750303080 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102287163 | CAGAATGAGACCCAA[-/T]TTAAAAAAAAAAAAA | 51366 |
rs750304860 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102393800 | CCGAGCATGGTGGCA[C/G]ACGCCTGGAGTCCCA | 51366 |
rs750312665 | snp | C/T | 1.64901e-05 | 0.00287137 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102279132 | GAATGTCATGGAGTC[C/T]GAACGTCGGAAAAAT | 51366 |
rs750314333 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102359022 | TCAACAGATCCACTC[-/A]ACCTTGGCCTCCCAA | 51366 |
rs750339514 | snp | A/G | 1.65787e-05 | 0.00287907 | intron-variant | UBR5 | GRCh38.p7 | 8:102270024 | TTAAGAGGTAACTAA[A/G]TACACAGTACACACT | 51366 |
rs750354454 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102316047 | AACGTAATTAGAAAG[C/T]CTATAAATCTTTTTT | 51366 |
rs750358422 | snp | C/G | 1.78908e-05 | 0.00299084 | intron-variant | UBR5 | GRCh38.p7 | 8:102323286 | ACTGGTGTCAAAGCA[C/G]GATTAGTTAAGCTAT | 51366 |
rs750358672 | snp | A/C | 1.73927e-05 | 0.0029489 | intron-variant | UBR5 | GRCh38.p7 | 8:102345589 | CATACACACAAAGAG[A/C]AACTGTAGACTGCTG | 51366 |
rs750364268 | snp | A/G | 3.30994e-05 | 0.004068 | intron-variant | UBR5 | GRCh38.p7 | 8:102270195 | GTCTCTGTAAGAGAA[A/G]GAAAACTATTATGAC | 51366 |
rs750420662 | snp | C/G | 1.65162e-05 | 0.00287365 | intron-variant | UBR5 | GRCh38.p7 | 8:102295564 | TGTCGTGAGGAGGGA[C/G]GCTGAAAAGCTACTC | 51366 |
rs750422962 | in-del | -/T | 1.66297e-05 | 0.0028835 | intron-variant | UBR5 | GRCh38.p7 | 8:102326518 | GAGAAACGAGGTCCC[-/T]TTAAGACAGGCTAAA | 51366 |
rs750423352 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102284703 | AAAGTCTAAACGCAT[C/T]TAATACCCCCAATAA | 51366 |
rs750427338 | snp | A/G | 1.85334e-05 | 0.00304407 | intron-variant, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102258945 | CTGACTGACCTATCT[A/G]TATAGTTCATTCTTT | 51366 |
rs750437180 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102383493 | GAATGCTTACAGCCA[C/T]GCTCTTACCTGCCAG | 51366 |
rs750454150 | snp | C/T | 1.64993e-05 | 0.00287218 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102259073 | CCTAAAATCTTCTGC[C/T]GTTAAATCTTCTAAT | 51366 |
rs750465456 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102290607 | CATCCACAAGAACTA[C/T]AGGCCCCTCAAAGTG | 51366 |
rs750467368 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102353658 | CTCATTAATTGTAAC[A/T]CATGTACCATACTAA | 51366 |
rs750477263 | snp | A/T | 1.66076e-05 | 0.00288158 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102323447 | TCCCAGCACTAATTG[A/T]AAATGCAACTGCTCC | 51366 |
rs750533700 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102352858 | AAACACTCAAATTCT[C/T]TTCTATAAGCACTGC | 51366 |
rs750545886 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102257874 | AGAAATTAAGAGCAT[A/T]TGCATAATGCAAAAC | 51366 |
rs750561315 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102372736 | CTGCAAACTAGAGAA[A/C]AATTACATTATTCAT | 51366 |
rs750570157 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102394744 | TCTTTGTAGCCACAA[A/T]ATCAAGCAACTTGCC | 51366 |
rs750635401 | in-del | -/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102310537 | TTTTCAGTAGAGATA[-/G]GGTTTCACCATGTTG | 51366 |
rs750635938 | in-del | -/TG | | | intron-variant | UBR5 | GRCh38.p7 | 8:102364205 | TGCCTCTTTTGAGAC[-/TG]GGTCTCACTCTGTCG | 51366 |
rs750643863 | snp | C/T | 1.823e-05 | 0.00301905 | intron-variant | UBR5 | GRCh38.p7 | 8:102298346 | ATGGACAGAAGAGAA[C/T]CTATCCAAACTGAAT | 51366 |
rs750650547 | snp | C/T | 1.71675e-05 | 0.00292976 | intron-variant | UBR5 | GRCh38.p7 | 8:102298810 | AAAAGCTAAGCTAAG[C/T]TAAATCTTCACATGA | 51366 |
rs750665102 | snp | C/T | 1.65842e-05 | 0.00287955 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285145 | CTGCCTTCAAGTGTT[C/T]GTAAGCTAGCTTCTT | 51366 |
rs750675912 | snp | C/T | 1.69697e-05 | 0.00291283 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102294101 | CACTAGTGTACCTAG[C/T]AGAGTATCTAAAAGC | 51366 |
rs750679713 | snp | A/G | 3.37223e-05 | 0.00410609 | intron-variant | UBR5 | GRCh38.p7 | 8:102275857 | AAGGGAAGGGGTGGG[A/G]GGGAGAAATAATTTA | 51366 |
rs750690260 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102340742 | CCAGAATTCAAGTAT[A/G]AATTTCTAGATTTCC | 51366 |
rs750699420 | snp | C/G | 1.65228e-05 | 0.00287422 | intron-variant | UBR5 | GRCh38.p7 | 8:102329259 | GTAGAGCTATTCAAT[C/G]CAAGATTTCATAAAA | 51366 |
rs750705521 | snp | C/T | 1.68633e-05 | 0.00290368 | intron-variant | UBR5 | GRCh38.p7 | 8:102265097 | AGATTAAAGTTCTTT[C/T]ACCTGCCAATGTTTC | 51366 |
rs750724897 | snp | C/T | 1.65693e-05 | 0.00287826 | intron-variant | UBR5 | GRCh38.p7 | 8:102360694 | AAACAGAAAAAATTA[C/T]CCAAGTAAAAATGTG | 51366 |
rs750768684 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102341596 | AGAAATCCATATCAG[C/G]CTCTCTTTATCTGCT | 51366 |
rs750769579 | snp | C/T | 1.64754e-05 | 0.00287009 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102276995 | TGTGAGAGGTGGCCC[C/T]TCACTTTCAGTAAGT | 51366 |
rs750803052 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102374185 | GGCAGCCATTTATCA[A/G]TATTACTGAAATGTA | 51366 |
rs750813050 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102328853 | GATCCACCCACCTCA[A/G]CCTCCCAAAGTGCTC | 51366 |
rs750818686 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102359157 | TCCTCCATTTAATTA[C/T]ATTTTGAAACTAGTT | 51366 |
rs750821018 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102264916 | GGGTTTCGCCATGTT[A/G]CCCAGGCAGGTCTCC | 51366 |
rs750830374 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102391597 | ATATAGCAAAATCTT[A/C]GTAAGTTAGGCAGGA | 51366 |
rs750911534 | snp | A/C | 3.67843e-05 | 0.00428845 | intron-variant | UBR5 | GRCh38.p7 | 8:102265329 | CACTGAAAAAACAAA[A/C]CATATGAAATGGTTC | 51366 |
rs750914337 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102285447 | TAATTCCCCTAATAC[G/T]GGAATTCTCATAATT | 51366 |
rs750923557 | snp | A/G | 1.64757e-05 | 0.00287012 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102313815 | AAACCTTGCCAACAG[A/G]AACATTCTTGACATC | 51366 |
rs750927180 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102252567 | ATCTTTCAAACACAT[C/T]GATGCTAATCAGCTC | 51366 |
rs750927231 | snp | A/G | 1.65143e-05 | 0.00287348 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102286572 | TCACTTGAGTCATTC[A/G]ATTGAGAATCATCTT | 51366 |
rs750936999 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102344048 | ACCACAGATCTGTTA[C/T]TTTAAAACTTTATTC | 51366 |
rs750943927 | snp | C/T | 1.64887e-05 | 0.00287125 | intron-variant | UBR5 | GRCh38.p7 | 8:102287411 | GCATAAGCAAGAAAG[C/T]AGTTGGGATAAGGCA | 51366 |
rs750954251 | snp | G/T | 3.30306e-05 | 0.00406377 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102280421 | CATCATCATTTTCAT[G/T]TTCTGAATCTTCATT | 51366 |
rs750955270 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102312041 | GGGAACAAAAAAATG[C/T]CAATGCCCTGAATTA | 51366 |
rs751003425 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102348820 | AAAAGTTTGGAATAC[A/G]TTAACCAATAATGAT | 51366 |
rs751006902 | snp | A/G | 3.41419e-05 | 0.00413156 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102254311 | TATACTCTACACAAA[A/G]CCAAAATTCTTGGTC | 51366 |
rs751018661 | snp | A/G | 3.41163e-05 | 0.00413001 | intron-variant | UBR5 | GRCh38.p7 | 8:102264450 | GCAATTGTGAATACA[A/G]TTAGGTTCATCAAAA | 51366 |
rs751034998 | snp | A/C/T | 4.98702e-05 | 0.0049933 | intron-variant | UBR5 | GRCh38.p7 | 8:102312313 | GTCAGTTCCAATATT[A/C/T]ACTTGCTGAATAACT | 51366 |
rs751038505 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102336263 | TATAAATTTTGAATA[G/T]TAACTCCTTATGACA | 51366 |
rs751047285 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102356800 | AAGTAAACAAATAAA[A/G]AAATGGGGTAGAGGA | 51366 |
rs751051035 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102388552 | TAACGTGCTGATGAC[A/G]TCATAACAAGATTTG | 51366 |
rs751060244 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102309654 | CTGTGTTACAAATGC[C/G]TACGGTATCCAGTAC | 51366 |
rs751061554 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102263654 | GCATGCTGTGTTGTA[C/T]TTCTTACATTCTTTG | 51366 |
rs751064353 | snp | A/C | 1.64866e-05 | 0.00287106 | intron-variant | UBR5 | GRCh38.p7 | 8:102329086 | AATGCAAAGTGTTTC[A/C]TACCTTGTTATTTTC | 51366 |
rs751065424 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102358447 | AAAATGTTCATCTTT[A/C]AGAAAGGTACTATTT | 51366 |
rs751077824 | snp | A/G | 1.65395e-05 | 0.00287567 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102294061 | CTTCTCTACGTCCAG[A/G]TGTATATTTGTTTTG | 51366 |
rs751107568 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102395420 | ACACACACACGTACC[-/T]TGTTTACATATACAC | 51366 |
rs751120156 | in-del | -/AATA | 2.4443e-05 | 0.00349584 | intron-variant | UBR5 | GRCh38.p7 | 8:102286658 | AAACATTGTGAGTTT[-/AATA]ATTAAAATTACAATG | 51366 |
rs751151861 | snp | A/C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102375681 | CCTCCCCTGCGGTTT[A/C/G]TATCTGGGCTGGTGT | 51366 |
rs751155901 | snp | C/T | 1.65165e-05 | 0.00287367 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102300125 | GCTGCTCTCAACGAA[C/T]GTCTCATCATTTCCC | 51366 |
rs751162211 | snp | C/T | 1.76708e-05 | 0.00297239 | intron-variant | UBR5 | GRCh38.p7 | 8:102285824 | AGCTAATGTCAGTTG[C/T]TAATTGTGTTTCTCT | 51366 |
rs751195626 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102397220 | GTCTTCAAAGTCTTT[C/T]CTACACAACCATTAG | 51366 |
rs751199439 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102364085 | CTACCTGGACTCACT[-/A]AAAGTCCACTAGGTC | 51366 |
rs751199886 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102271328 | CAATGCAAAGAAATG[-/A]GACAAATGTAAGAAA | 51366 |
rs751204108 | snp | A/G | 1.64814e-05 | 0.00287061 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102312445 | TTACTGGAGGTTCCT[A/G]GAAATTTTACAGCAA | 51366 |
rs751209790 | in-del | -/A | 1.7058e-05 | 0.0029204 | intron-variant | UBR5 | GRCh38.p7 | 8:102277230 | GTTACAAATGAAGGG[-/A]AAAAAACTAATTAGA | 51366 |
rs751219997 | in-del | -/CT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102276596 | GTCCACAATTCTCCC[-/CT]GTCTTACATCGTTAT | 51366 |
rs751247760 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102316232 | AGCAGTAAACTTAGT[A/C]AATTTATAATCATAA | 51366 |
rs751248429 | snp | C/T | 4.96997e-05 | 0.00498472 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102286401 | GCTGTACTGGCTGCT[C/T]GCTGATGCTGGGTGT | 51366 |
rs751248724 | snp | A/C/G | 3.29904e-05 | 0.00406132 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295496 | CACCGTCTGCCTTGC[A/C/G]ACTGTCTGTACTAAG | 51366 |
rs751252809 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102347150 | ATTCTGATTGCTTGG[C/T]TTTCATTATTATTAT | 51366 |
rs751276029 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102264679 | TCTATTCAGCATAAA[C/G]TACAGCACATACACT | 51366 |
rs751280307 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102285107 | TTGGGGACGTTCTGT[A/G]TATATGAAGAATTTC | 51366 |
rs751296170 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102297826 | CACATATGATGCCAA[C/T]ACAAACACACTATAC | 51366 |
rs751302705 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102352955 | AGTTTAAAGACAACC[A/G]TCAAAATATCTCTCC | 51366 |
rs751328722 | snp | C/T | 1.66172e-05 | 0.00288242 | intron-variant | UBR5 | GRCh38.p7 | 8:102270221 | ATGACTTCATTTCCT[C/T]TGACTAACAAGTAAA | 51366 |
rs751331210 | snp | A/C | 3.34415e-05 | 0.00408896 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102304018 | TTTTCCTCCAATTAA[A/C]GTTTCCTGGTAAAAA | 51366 |
rs751358792 | snp | A/G | 1.68681e-05 | 0.00290409 | intron-variant | UBR5 | GRCh38.p7 | 8:102280347 | GAAGGGGAACTACTG[A/G]GGCAGCCATTTCTTG | 51366 |
rs751378686 | snp | C/G | 1.71838e-05 | 0.00293114 | intron-variant | UBR5 | GRCh38.p7 | 8:102346420 | AAAATAAAAAGAAGT[C/G]CTATGGTAATTTTCT | 51366 |
rs751379491 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102334372 | TCTTGGCTCACTGCA[A/G]CCTCCGCCTCCTGCG | 51366 |
rs751389597 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102263100 | CAAAAAAAAAAAAAA[-/T]TTAATTAATTAAAGC | 51366 |
rs751409551 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102365681 | TCATTCCTTTAAATG[C/T]ATAGATCACTTTACA | 51366 |
rs751426768 | snp | A/T | 3.29522e-05 | 0.00405894 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102289541 | CGCCTCTGCTGTGGA[A/T]TCCTGATGATGTAGG | 51366 |
rs751427530 | snp | A/C | 1.66846e-05 | 0.00288826 | intron-variant | UBR5 | GRCh38.p7 | 8:102272485 | TGTTGGTTTGAGGAA[A/C]AAGGAAAGAATTTTA | 51366 |
rs751427636 | snp | A/G | 1.6549e-05 | 0.0028765 | intron-variant | UBR5 | GRCh38.p7 | 8:102326537 | AGACAGGCTAAATCC[A/G]TCACTTACCTGGGTA | 51366 |
rs751428431 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102259611 | TCATTTTGCAGAGGA[C/G]GGAACCAAGGCACAA | 51366 |
rs751457674 | in-del | -/CAAAAAAC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102392623 | AAAAAAAAAAAAAAA[-/CAAAAAAC]AAAAAACAAAAACTT | 51366 |
rs751465084 | snp | C/T | 1.67119e-05 | 0.00289062 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102323467 | GCAACTGCTCCAGCA[C/T]GATAAAGAGGATTAT | 51366 |
rs751472569 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102395716 | GAAACATCTCAAAAC[-/A]TTCTATTCAGCAGTG | 51366 |
rs751483045 | in-del | -/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102371584 | GATTCTGGGTTGTTT[-/G]TTTTTTTTTTTTTTG | 51366 |
rs751494589 | snp | G/T | 8.25089e-05 | 0.00642243 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102259098 | TCTAATGAATTTTTT[G/T]GAAGCACATCTAGTA | 51366 |
rs751504195 | in-del | -/A | 1.75789e-05 | 0.00296465 | intron-variant | UBR5 | GRCh38.p7 | 8:102346858 | ATTCAGTAAAACCTC[-/A]CCTTGTCCTGTTGTC | 51366 |
rs751521594 | snp | A/C | 1.71278e-05 | 0.00292637 | intron-variant | UBR5 | GRCh38.p7 | 8:102261122 | GCCTCATTGGATCAC[A/C]CAACACTTTCTAGAA | 51366 |
rs751550324 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102390499 | AAAAAAAAAAGCCAC[A/G]CTTTTATATATACAA | 51366 |
rs751555469 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102270920 | AATATAATTTCAACC[G/T]CCTCTGGGTTTTTAA | 51366 |
rs751570928 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102374279 | GGTTCTCAAACTAAA[C/T]AGGGCCTTATTTGAT | 51366 |
rs751572112 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102329207 | TGAAGGATTCTTTGA[A/G]AGCATAAAAAAAAAT | 51366 |
rs751589998 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102353718 | ACATGGGGTACATGG[C/G]AACTCTCAGTATGAT | 51366 |
rs751628497 | snp | A/G | 1.69086e-05 | 0.00290758 | intron-variant | UBR5 | GRCh38.p7 | 8:102275861 | GAAGGGGTGGGGGGG[A/G]GAAATAATTTAGCCA | 51366 |
rs751638959 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102331451 | AATGAAAGCACCATT[C/T]TCACCTCCTCCCTTC | 51366 |
rs751643333 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102293553 | TTAGGAAGTCAAACA[C/T]GACATTTCCAGAGAA | 51366 |
rs751649172 | snp | A/G | 1.64811e-05 | 0.00287059 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311807 | GCTTGTAGGAAAATT[A/G]TTTTCCTGTTCTGCT | 51366 |
rs751668775 | snp | C/T | 1.67618e-05 | 0.00289493 | intron-variant | UBR5 | GRCh38.p7 | 8:102298845 | TATATCAAATCCTCT[C/T]ACTTGGCAGAAAGAA | 51366 |
rs751671319 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102266666 | TTTCCCTCTCTGTTC[G/T]TCAATTTGTTACTTA | 51366 |
rs751673260 | in-del | -/CCT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102377256 | TCTAGAACATAGAAA[-/CCT]CCTCCAAAAGGCACA | 51366 |
rs751681149 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102340908 | AAGGAATAATGCACT[A/G]AAAGTCTATACAGTG | 51366 |
rs751694124 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303465 | CATTAGCACATAGTG[A/C]GCAGTGCTTCCATTA | 51366 |
rs751695964 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102361393 | CTGTATGCCAGATTT[A/T]AAAAAAAAAAAGCAT | 51366 |
rs751697183 | snp | C/T | 1.66527e-05 | 0.00288549 | missense, nc-transcript-variant, intron-variant | UBR5 | GRCh38.p7 | 8:102285293 | TAGAATCCATAATAC[C/T]GACCATCCAGTTCCA | 51366 |
rs751698824 | snp | G/T | 1.65949e-05 | 0.00288048 | intron-variant | UBR5 | GRCh38.p7 | 8:102360699 | GAAAAAATTATCCAA[G/T]TAAAAATGTGTATTA | 51366 |
rs751700592 | snp | G/T | 8.60978e-05 | 0.0065606 | intron-variant | UBR5 | GRCh38.p7 | 8:102311913 | GCACATAAATGAGAA[G/T]AAAAATTGTTATACA | 51366 |
rs751707025 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102384770 | AAGTCTAAAAGGGCC[G/T]TGACCTTACTTCTCT | 51366 |
rs751746081 | snp | A/C/T | 5.04522e-05 | 0.00502235 | intron-variant | UBR5 | GRCh38.p7 | 8:102329438 | TAAATATAAAAATTG[A/C/T]CAAATCTACTGATTT | 51366 |
rs751752208 | in-del | -/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102368747 | GTGTCAGCCATCATG[-/C]CCAGCCTAGGAGGGT | 51366 |
rs751763604 | in-del | -/TAG | | | intron-variant | UBR5 | GRCh38.p7 | 8:102265477 | AAGCTTGTGTATTAT[-/TAG]TAGGTCTTTAACGTC | 51366 |
rs751767566 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102282160 | GGCAACAGAGCGAGA[A/C]CCTGTCTCAAAAAAC | 51366 |
rs751772147 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102281720 | CAGTATCCTTTGGAA[C/T]GGCAAAATGAATTCT | 51366 |
rs751785724 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102330142 | TCTTTAACATAAAAC[A/G]AATGATCAGAGCCAC | 51366 |
rs751791635 | snp | A/G | 1.64735e-05 | 0.00286993 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102277028 | TATTTCTGCTAGTAA[A/G]CTACTTTTTAATTGT | 51366 |
rs751797809 | snp | C/G | 1.65329e-05 | 0.0028751 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295094 | AAAAGATGGCCTATT[C/G]TACTGCTGGCACTAA | 51366 |
rs751818396 | snp | A/G | 1.64735e-05 | 0.00286993 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102313840 | GACATCTTCCACAAA[A/G]ACCACTTCCCGAAGA | 51366 |
rs751824953 | snp | C/T | 1.65545e-05 | 0.00287697 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102298951 | CCTTGGATTCTACTA[C/T]AGATGGCTCTGTGGA | 51366 |
rs751833952 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102311200 | TAGGGAAGAAAGGGG[C/T]AATGAATGATCTATT | 51366 |
rs751874303 | snp | C/G | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102305135 | AAGCAAACTGATACA[C/G]AAGCATGCAAAATAT | 51366 |
rs751874877 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102344419 | CCCGGGTTCATGCCA[G/T]TCTCCTGCCTCAGCC | 51366 |
rs751894318 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102280223 | TTAGTTGTGAAATGT[A/G]TAACGCAAGAATGTG | 51366 |
rs751897395 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102409342 | GATACTTTTTTATGC[-/T]TTGTACATTTTAGAC | 51366 |
rs751913107 | snp | A/G | 1.64841e-05 | 0.00287085 | intron-variant | UBR5 | GRCh38.p7 | 8:102287423 | AAGTAGTTGGGATAA[A/G]GCAACATACCTGCTT | 51366 |
rs751920203 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102379738 | GCAGATATGCAAACC[A/C]GTAGAGTGAAAGAAT | 51366 |
rs751920755 | snp | C/T | 1.64982e-05 | 0.00287208 | intron-variant | UBR5 | GRCh38.p7 | 8:102267050 | AGATAACGGAGACTT[C/T]TAGAATTTAGCGTAT | 51366 |
rs751926630 | snp | C/T | 1.65855e-05 | 0.00287967 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102254338 | GGTCTTAATGGCGAG[C/T]AACAATTTCTGTTTG | 51366 |
rs751958076 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102288868 | TACTAAATTTTTCTA[A/G]CATTACGAATATCTT | 51366 |
rs751988190 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102348983 | TGTCATCCTTTTGAC[A/G]AGCTTCTGTACTTGC | 51366 |
rs751996840 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102410255 | ACCGCAAAATAGGTT[C/T]TGGCATGCACAGCCA | 51366 |
rs751997070 | in-del | -/TCT | | | utr-variant-3-prime, downstream-variant-500B, cds-indel | UBR5 | GRCh38.p7 | 8:102253793 | AAAAGTGATTTCATC[-/TCT]TAAGATCTGAATGTC | 51366 |
rs752028111 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102391724 | GGAAATATGTCAGAA[A/G]CATTCAAACCACAGC | 51366 |
rs752034919 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102315270 | CAAGTAAGTAAAAAG[A/C]CCATTAGACCATTAA | 51366 |
rs752043188 | in-del | -/ATAT | | | intron-variant, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102276917 | GGTAACTAGACATGG[-/ATAT]ATATTTTTAACGCTG | 51366 |
rs752055021 | snp | C/T | 3.33034e-05 | 0.00408051 | intron-variant | UBR5 | GRCh38.p7 | 8:102281273 | CTTAAATCAACCTCA[C/T]GGCAAGAATGGATAC | 51366 |
rs752061545 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102272949 | ACAATACTTTAAAGC[A/C]TACAAGAATGTCTTG | 51366 |
rs752071405 | snp | A/G | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102281388 | GCCACATGCTTCAAT[A/G]AGCAAACATCCAAAA | 51366 |
rs752084163 | snp | C/T | 1.8644e-05 | 0.00305314 | intron-variant | UBR5 | GRCh38.p7 | 8:102257588 | ACATGGTATTTTTAA[C/T]TTCTGTATTTCCTTC | 51366 |
rs752089305 | snp | A/G | 1.64746e-05 | 0.00287002 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102305238 | GCTCAAGATTCATTA[A/G]ATATTGTCGACAGGC | 51366 |
rs752095381 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102323096 | AAGTATAATAATAAT[A/T]AATTAATTAATTAAT | 51366 |
rs752096715 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102383104 | TGGCCAGTGAGTTCA[C/T]GACAAGAGAAAACTT | 51366 |
rs752097589 | snp | G/T | 1.65436e-05 | 0.00287602 | intron-variant | UBR5 | GRCh38.p7 | 8:102288135 | CTCATACTGAGTAAT[G/T]TCTCAAATAACCTGC | 51366 |
rs752099216 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102269619 | TCATATCATATAAAG[-/A]AAAACTCTTGATAGA | 51366 |
rs752115857 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102258150 | CAAGATCTTAGGCAG[-/T]TTATTTGGATACTGT | 51366 |
rs752121784 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102252608 | TACTATTTCATTTAT[G/T]CAGAAATAGCATTTA | 51366 |
rs752130865 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102302078 | GCTGTGATGTAGTCA[A/G]TTCAATATTAAATGA | 51366 |
rs752142676 | snp | A/G | 1.6501e-05 | 0.00287232 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102347039 | CGAGCTCCAGCTGAT[A/G]ACCTACCAGAGGATC | 51366 |
rs752149509 | snp | A/C | 1.66868e-05 | 0.00288845 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102296943 | TTCCGTACAACAACA[A/C]AGTGACTCCAGCAAG | 51366 |
rs752157339 | in-del | -/TTTT | 1.73776e-05 | 0.00294762 | intron-variant | UBR5 | GRCh38.p7 | 8:102261909 | AAAGTGTATATTTGC[-/TTTT]TTTACCTGTCCTCCA | 51366 |
rs752158081 | snp | C/T | 3.30186e-05 | 0.00406303 | missense, upstream-variant-2KB, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102304082 | CGATTACCTGGGCCA[C/T]TACTTGAAACAACTG | 51366 |
rs752160243 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102347308 | TATGTCACCCAGGCT[A/G]GAGAGCACTGGTTAT | 51366 |
rs752190827 | snp | C/T | 1.64833e-05 | 0.00287078 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102286551 | TGACTACTACTGCTA[C/T]CAGAATCACTTGAGT | 51366 |
rs752200218 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102334512 | GGCCAGACTGGTCTC[A/G]AACTCCTGACCTCAA | 51366 |
rs752202635 | snp | G/T | 0.000149702 | 0.00865035 | intron-variant | UBR5 | GRCh38.p7 | 8:102311725 | TTCAAAAGCAAAAAT[G/T]AGCCTCTACCTGTCC | 51366 |
rs752204857 | snp | A/G | | | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102298876 | GTTCTCGTAGATAGG[A/G]CTGGAGAACCACACT | 51366 |
rs752206822 | snp | A/G | 1.6495e-05 | 0.0028718 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102312462 | AAATTTTACAGCAAC[A/G]TAGGCACCATCTACT | 51366 |
rs752217825 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102377850 | GGAGACAGCAATAGA[A/T]TTCAGTATTGTTTTT | 51366 |
rs752217920 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102378849 | CTCACCCCATCTCAA[C/T]GCCCACTCTCATCTT | 51366 |
rs752239775 | in-del | -/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102283342 | TAGGAAGGGGAAGGC[-/G]GGGGGGGGGGGGGGT | 51366 |
rs752240198 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102379410 | CAAACCTAACAAAAT[A/G]GAGGCAGTCTTATTA | 51366 |
rs752263919 | snp | A/G | 3.29853e-05 | 0.00406098 | intron-variant | UBR5 | GRCh38.p7 | 8:102313791 | AATTAAGTTTTAGAT[A/G]TCTTGAACAAACCTT | 51366 |
rs752281125 | snp | C/T | 1.65258e-05 | 0.00287448 | intron-variant | UBR5 | GRCh38.p7 | 8:102295585 | AAAGCTACTCAGCTG[C/T]GCTGCGCTCTTTTGA | 51366 |
rs752297418 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102356449 | GGGAGACTCTGTCTC[-/A]AATTAGATAGATAAA | 51366 |
rs752335293 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102380502 | ATAGATTAATCTCAC[A/T]TATTACAAGTCAAAG | 51366 |
rs752342920 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102366955 | AATCTGTGACCAGAT[A/G]AATTCTGCTAGAAAA | 51366 |
rs752377998 | snp | C/T | 3.51482e-05 | 0.004192 | intron-variant | UBR5 | GRCh38.p7 | 8:102346859 | TTCAGTAAAACCTCA[C/T]CTTGTCCTGTTGTCT | 51366 |
rs752381844 | snp | A/T | 1.67055e-05 | 0.00289006 | intron-variant | UBR5 | GRCh38.p7 | 8:102305047 | TCAAAATTGCCTAAA[A/T]CTCCCTTTAAAGACC | 51366 |
rs752396367 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102316290 | AAACAATTTTGGAAC[C/T]TTAAAAATCTGTATG | 51366 |
rs752405256 | snp | A/G | 1.65444e-05 | 0.00287609 | intron-variant | UBR5 | GRCh38.p7 | 8:102272512 | TTTAAGCTGCTTGTT[A/G]TTTGTAGAGTACTTA | 51366 |
rs752405793 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102385032 | TTACAGCACATAATA[C/T]GCTTAGTACAGAGCC | 51366 |
rs752430967 | snp | A/C | 1.64781e-05 | 0.00287033 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102346975 | GCCCAAAAGCCCAGA[A/C]CCTCGATCCCGTCCT | 51366 |
rs752434906 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102252404 | AAGACATTGTGCATT[A/G]TTTTAAATATTTTCA | 51366 |
rs752436817 | snp | A/G | 1.656e-05 | 0.00287745 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295688 | GCAGGCGATAAAGTA[A/G]ATCAAGACGAGCAGA | 51366 |
rs752438322 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102368061 | TTCGGTACTCCAACT[G/T]TGGGATTTCATGGTG | 51366 |
rs752479789 | snp | C/T | 1.6495e-05 | 0.0028718 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102326560 | CCTGGGTACCAACAG[C/T]GATGTTCGGCATTGA | 51366 |
rs752489028 | in-del | -/AAGTA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102410485 | AAAAGATCTTTAATG[-/AAGTA]AAGTCAGGCTAAGAA | 51366 |
rs752503629 | snp | C/T | 1.68383e-05 | 0.00290153 | intron-variant | UBR5 | GRCh38.p7 | 8:102326684 | AACAAAAAACATAAA[C/T]TGGTCAAATAAGCAG | 51366 |
rs752523005 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102259838 | GGCCAAGGTGGGCAG[A/G]TCATGAGATCAAGAC | 51366 |
rs752535637 | snp | A/T | 1.70577e-05 | 0.00292037 | intron-variant | UBR5 | GRCh38.p7 | 8:102293581 | GAAGGATTAATCAGA[A/T]TCTGTTACCTGGTAG | 51366 |
rs752556696 | snp | C/T | 3.49626e-05 | 0.00418092 | intron-variant | UBR5 | GRCh38.p7 | 8:102311925 | GAAGAAAAATTGTTA[C/T]ACATCTTATCTCTAA | 51366 |
rs752585690 | snp | C/T | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102277053 | AATTGTGCAGCAAGA[C/T]CATGAGCAGATGGCC | 51366 |
rs752586346 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102374388 | ACACACTGTAACTCC[C/T]TGTTTCTTATACACG | 51366 |
rs752591853 | in-del | -/GAT | 5.10208e-05 | 0.00505053 | intron-variant | UBR5 | GRCh38.p7 | 8:102299417 | TCCTTTTTTCTTCCA[-/GAT]GATGACTAGGCAGAC | 51366 |
rs752606434 | snp | C/T | 1.64906e-05 | 0.00287142 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311826 | TCCTGTTCTGCTTTT[C/T]CTGTAGCAAGATCAA | 51366 |
rs752609322 | in-del | -/GAGGAGGC | | | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102413028 | TAAGTGTGTGTCCCA[-/GAGGAGGC]GAGGAGGAAGAGGGG | 51366 |
rs752625481 | snp | C/T | 1.67237e-05 | 0.00289164 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102293706 | ACTAGCCAGGGTAAA[C/T]GGTGCAGTTGGACGA | 51366 |
rs752635290 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102386129 | TGAACAGTGGTCCCT[A/G]TTTCAATATTCAAAT | 51366 |
rs752644980 | snp | C/T | 6.669e-05 | 0.00577413 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102293825 | GCTTGCATTTTCCAA[C/T]TGGCTGTGGAATAAA | 51366 |
rs752654362 | snp | A/C | 1.76899e-05 | 0.00297399 | intron-variant | UBR5 | GRCh38.p7 | 8:102261874 | ACAGCAGTTTAACCA[A/C]ATTCTCTTGCCAGAA | 51366 |
rs752657660 | snp | C/T | 1.64841e-05 | 0.00287085 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295440 | GCTGTTTTTCGGTTA[C/T]GATCTTCCCTGATTC | 51366 |
rs752680025 | in-del | -/CAT | 3.55511e-05 | 0.00421596 | intron-variant | UBR5 | GRCh38.p7 | 8:102323518 | ACAAAAGAAAACCAC[-/CAT]CAAGATGACATAACT | 51366 |
rs752723840 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102342324 | ATATTCTATCTATAT[C/T]TTAAAACAAAACAAA | 51366 |
rs752749439 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102307373 | AGACCACAGCTACCT[A/C]TGTATCATCACCTCC | 51366 |
rs752759685 | snp | A/G | 1.66502e-05 | 0.00288527 | intron-variant | UBR5 | GRCh38.p7 | 8:102312295 | CCATAATAAACTCAC[A/G]GAGTCAGTTCCAATA | 51366 |
rs752762381 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102362543 | AGAAAAGTCCATGAA[C/T]TCTGCTCTCTAAAGA | 51366 |
rs752765697 | snp | A/G | 1.66153e-05 | 0.00288225 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102361198 | TCCAATACATTCAAA[A/G]GGGGGTGGCTGAGAG | 51366 |
rs752780128 | snp | A/G | 1.65037e-05 | 0.00287256 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102277169 | TTTCAGATTGGCAGC[A/G]TAAGACATTTTTGTT | 51366 |
rs752789203 | snp | A/G | 1.66136e-05 | 0.00288211 | intron-variant | UBR5 | GRCh38.p7 | 8:102298974 | TCTGTGGAAGGACCT[A/G]TAATTAAGCAGATTC | 51366 |
rs752792141 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102254612 | TAAAAGGAGATATTA[C/T]TTTGAACTGGATTTT | 51366 |
rs752832665 | snp | A/T | 1.64893e-05 | 0.0028713 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102342638 | ACGTAAAACGGATTC[A/T]CGTTCACGCAACAGC | 51366 |
rs752844585 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102343971 | ATTTAAGGCAGTAAA[C/G]TATGCATTTATTTTT | 51366 |
rs752861923 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102403350 | CCAGGAGTTCGAGAC[C/T]AGCCTGGGCAACACA | 51366 |
rs752872119 | in-del | -/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102373201 | GCTCCGTTCGAAACA[-/G]GAAAAGGAAAAGAAT | 51366 |
rs752881809 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102404725 | CCAGCCTGACCAACA[C/T]GGTCAAACCCCGTCT | 51366 |
rs752886917 | snp | A/G | | | intron-variant, utr-variant-5-prime | UBR5 | GRCh38.p7 | 8:102302333 | CTGCTAAGATTCAGA[A/G]TTTTGACATTTCTTC | 51366 |
rs752888604 | snp | A/C | 8.23839e-05 | 0.00641757 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102342544 | TATTCTTCTTATCCA[A/C]GTTTGGCTCTCCTTC | 51366 |
rs752894811 | snp | A/G | 1.64999e-05 | 0.00287222 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102287500 | ATTATCTTGGTTGCT[A/G]TGGTTACTTTCACTA | 51366 |
rs752904135 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102350628 | AAACATAAGGGAAAA[A/G]CTTCATGGACTTGGT | 51366 |
rs752905809 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102284861 | CTAACACAGTGAAAC[C/G]CCGTCTCTACTAAGA | 51366 |
rs752912061 | in-del | -/TC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102256389 | AGATAGCCAATCCTT[-/TC]TGTTTTTGGTGGTTC | 51366 |
rs752933051 | snp | A/G | 1.66718e-05 | 0.00288715 | intron-variant | UBR5 | GRCh38.p7 | 8:102269988 | ATCTTTAATTCAAAA[A/G]CAAAAAAATAACACA | 51366 |
rs752961363 | in-del | -/A | 1.65811e-05 | 0.00287929 | intron-variant | UBR5 | GRCh38.p7 | 8:102360697 | CAGAAAAAATTATCC[-/A]AGTAAAAATGTGTAT | 51366 |
rs752961578 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102405258 | AAATCAGATTGGCCA[C/T]GAGTTGACAACTGTT | 51366 |
rs753009741 | snp | C/T | 0.000182565 | 0.00955244 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102323444 | GAATCCCAGCACTAA[C/T]TGAAAATGCAACTGC | 51366 |
rs753011527 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303585 | TAGCAATTTTTAATG[C/T]GTTATAAAAGTTTGT | 51366 |
rs753013494 | snp | C/T | 1.65941e-05 | 0.00288041 | intron-variant | UBR5 | GRCh38.p7 | 8:102314885 | GATTCTCCTTATAAT[C/T]AGATAAATGAAATAA | 51366 |
rs753038838 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102259721 | TGCACAATTATTGTA[A/G]CACAGGGATCAGAAA | 51366 |
rs753043356 | snp | C/T | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102281413 | CCAAAACTGGAAGAA[C/T]ATCAGAATGCTCATC | 51366 |
rs753060660 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102325731 | AAGTTTTAAATATTT[A/T]ATAGTGATAAAACCC | 51366 |
rs753067079 | snp | C/T | 3.29478e-05 | 0.00405867 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311371 | ATTTATTAAAGAATG[C/T]ACACCCATTCCAAGA | 51366 |
rs753102922 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102337935 | TGTTATACAACCACC[A/T]AATTAAAAGATTACC | 51366 |
rs753156216 | in-del | -/TTGA | | | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102253621 | GATACAAAGAAAAAG[-/TTGA]TTGATTGTGATAAAA | 51366 |
rs753167492 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102393523 | CGCCAGTAGTCCCAG[C/T]TACTCAGGAGGCTGA | 51366 |
rs753182023 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102380882 | TGTATTAGTCTGTTT[C/T]CACACTGCTATAAAG | 51366 |
rs753185529 | snp | A/C | 1.80863e-05 | 0.00300713 | intron-variant | UBR5 | GRCh38.p7 | 8:102275499 | CTACAGGTATAGTAT[A/C]AGAAAATCTAAATAC | 51366 |
rs753188275 | snp | A/G/T | 3.34466e-05 | 0.0040893 | intron-variant | UBR5 | GRCh38.p7 | 8:102297642 | CAGTTCATCTTTCAG[A/G/T]AAAGGACTTAATTAG | 51366 |
rs753203869 | snp | G/T | 1.70345e-05 | 0.00291838 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102262066 | GCAAAATCATGCCAA[G/T]TGACCTAAAAAAGTA | 51366 |
rs753203949 | snp | G/T | 0.000115556 | 0.00760032 | intron-variant | UBR5 | GRCh38.p7 | 8:102275660 | GATTATTCCCTGAAA[G/T]ACATGCTTATCAGGC | 51366 |
rs753224947 | snp | A/C/T | 6.59232e-05 | 0.0057409 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102360169 | CGTCCTCCCTGCCCC[A/C/T]GAGTTGCTGTTCAAC | 51366 |
rs753228717 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102360889 | AATCTGACAAAATTC[A/G]AAGTAAGAAAATGAC | 51366 |
rs753233769 | snp | A/G | 1.66846e-05 | 0.00288826 | intron-variant | UBR5 | GRCh38.p7 | 8:102281524 | AGGTGGCACGTCTAT[A/G]AGAACAGAAAGGAAA | 51366 |
rs753238291 | snp | C/T | 3.30617e-05 | 0.00406568 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102297535 | ATAAAGGAGAGTCAT[C/T]AGGGTTGGTACCTGA | 51366 |
rs753251775 | snp | C/T | 1.702e-05 | 0.00291714 | intron-variant | UBR5 | GRCh38.p7 | 8:102281240 | TGTACTAAAGAAGAC[C/T]ATACCAAGCAAGTAT | 51366 |
rs753277160 | snp | C/T | 1.7494e-05 | 0.00295748 | intron-variant | UBR5 | GRCh38.p7 | 8:102346872 | CACCTTGTCCTGTTG[C/T]CTGACATTAAGTGTT | 51366 |
rs753313617 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102274116 | TGACTTTAAAACAAA[C/T]CTAATTTAACTGTGT | 51366 |
rs753320660 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102368303 | ACCAATGAGTAAGAC[G/T]GTTGTGATGGCCAAA | 51366 |
rs753335401 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102360575 | TATTAAATAGAAAGG[-/A]CATAATATCTTACCC | 51366 |
rs753337729 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102382602 | ATCAACAGAAGCCTC[A/G]CAAAATTAAATCTTG | 51366 |
rs753343861 | snp | C/T | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102346994 | CGATCCCGTCCTGTC[C/T]GAATAACTCGAGTCT | 51366 |
rs753352486 | snp | C/T | 1.6483e-05 | 0.00287076 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102272542 | ACTTGTGTGGGTGCC[C/T]TTGTTGGCATTTTGG | 51366 |
rs753357052 | snp | C/G | 1.64893e-05 | 0.0028713 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102305091 | TAATCTCACCCTCTT[C/G]TTCTTTAGTTTCTTT | 51366 |
rs753366048 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102254029 | CCCTCAGCAAAAAGA[C/T]AAATCACAGTGTAAA | 51366 |
rs753411170 | snp | C/T | 1.64868e-05 | 0.00287109 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102272685 | TTACTCTGTGTACAG[C/T]CATTGGTGTAGTAGC | 51366 |
rs753412107 | snp | A/G | 1.65751e-05 | 0.00287876 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295716 | AGATTTCTGTCCAGC[A/G]ATAAGAGTTTTACAT | 51366 |
rs753412708 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102379568 | AACCCTGATTGTCGA[C/T]AGTCAGTGTAAAAAC | 51366 |
rs753444969 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102259684 | CCATGATTTCAACTC[-/T]TAACAGTATGACTCC | 51366 |
rs753447524 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102369439 | TTATTGACTGACACA[C/G]ATACTCAAAAATCAC | 51366 |
rs753457669 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102307442 | AGCTAAGCTAAGAAT[C/G]AGTCTGGGTGTCTAA | 51366 |
rs753458007 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102357789 | CACATAAATTATTTG[-/T]GCTATTTTTGCAAAC | 51366 |
rs753459943 | snp | C/T | 1.69591e-05 | 0.00291191 | intron-variant | UBR5 | GRCh38.p7 | 8:102326697 | AATTGGTCAAATAAG[C/T]AGTAAAACAGCCCAC | 51366 |
rs753466637 | in-del | -/AAAAAAAA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102392608 | GGACTATTAGATACC[-/AAAAAAAA]AAAAAAACAAAAAAC | 51366 |
rs753469164 | in-del | -/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102383184 | TTTTTAGGAATTGGA[-/G]GGCATCACATTCCTC | 51366 |
rs753477573 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102273853 | ATGTAATTAATACAT[A/G]CATATGCTTATATGT | 51366 |
rs753487351 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102354930 | GGTCAGGAGTTAAAG[A/T]CCAGCCTGGGCAACA | 51366 |
rs753487814 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102397551 | CTAAAAATACAAAAA[A/G]TTAGCCAGGCATGGT | 51366 |
rs753536834 | snp | A/G | 1.743e-05 | 0.00295206 | intron-variant | UBR5 | GRCh38.p7 | 8:102296879 | AAACTAAAGAAAACT[A/G]GAATTGTACTCACTT | 51366 |
rs753552729 | snp | A/G/T | 3.36832e-05 | 0.00410374 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102293720 | ATGGTGCAGTTGGAC[A/G/T]AGCAATCCCCATTCT | 51366 |
rs753579011 | snp | G/T | | | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295664 | GAGTAACCAGATTAG[G/T]AGCAGTGAGCAGGCG | 51366 |
rs753580056 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102396775 | CAGTGGCGCGATCTC[A/G]GCTCACTGCAACCTC | 51366 |
rs753582372 | snp | A/C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102324924 | TACCAAGGTATTTTC[A/C/G]TATGTTATCTTTCGG | 51366 |
rs753585076 | snp | G/T | 1.79114e-05 | 0.00299255 | intron-variant | UBR5 | GRCh38.p7 | 8:102311934 | TTGTTATACATCTTA[G/T]CTCTAATAAACATCT | 51366 |
rs753585163 | snp | C/T | 1.64846e-05 | 0.0028709 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102327778 | AGCTGAGCGCAGGTG[C/T]AAAGGGCACAGCAAT | 51366 |
rs753592596 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102270522 | ATCTGCCAAAATTAA[A/T]TTTTTTTTTGCCAGA | 51366 |
rs753599740 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102261798 | TATCCATCTCTCCTA[C/T]GTGTACACACACGTT | 51366 |
rs753606676 | snp | A/C/T | 4.94575e-05 | 0.00497259 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102272682 | CTTTTACTCTGTGTA[A/C/T]AGCCATTGGTGTAGT | 51366 |
rs753625702 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102257519 | TGTGACCTTCTATAA[C/T]TGCCCTACCCAAAAT | 51366 |
rs753630699 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102386207 | GGCCAAGGCGGGTGG[A/T]TCACCTGAGGTCAGG | 51366 |
rs753671482 | snp | C/T | 1.67343e-05 | 0.00289255 | intron-variant | UBR5 | GRCh38.p7 | 8:102299006 | TTTGGTACAAAACAA[C/T]AATGAAGAAGACACA | 51366 |
rs753683632 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102342724 | GTGGGATAAAAGTAA[A/G]CCACTCTCTAGTAAA | 51366 |
rs753707063 | snp | A/G | 1.68786e-05 | 0.002905 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285768 | ATCAATATAAATCAA[A/G]CCCGCTGAACTTGCT | 51366 |
rs753708058 | snp | C/T | 6.61354e-05 | 0.00575007 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285573 | AATCTGAGAGTATAC[C/T]AGGTGATTATACTTA | 51366 |
rs753725141 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102362640 | CCAAAAATAAATGAC[A/G]TTAAAGCCAGTTTAG | 51366 |
rs753732455 | snp | A/G | 0.000133427 | 0.00816674 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102361202 | ATACATTCAAAGGGG[A/G]GTGGCTGAGAGATAA | 51366 |
rs753748949 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102405149 | TATTAAGGTTTTTTC[A/T]GGTTTTTTTTTAAAG | 51366 |
rs753753105 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102282893 | AAACTAAAACTCTCA[C/T]ACACACACTGCTACT | 51366 |
rs753756542 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102398601 | GTCTGGCCAACATGG[A/T]CAAACCCTGTCTCTA | 51366 |
rs753757058 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102376780 | AAGTGCTGGGATTAC[A/G]GGCACAACTTTTTAT | 51366 |
rs753760058 | snp | C/T | 1.65252e-05 | 0.00287443 | intron-variant | UBR5 | GRCh38.p7 | 8:102295366 | TGACCAAAACAAAAA[C/T]AAAACATATTGCTTC | 51366 |
rs753765928 | snp | G/T | 1.65485e-05 | 0.00287645 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102277184 | ATAAGACATTTTTGT[G/T]GGAAGAACCTATGAA | 51366 |
rs753778198 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102296438 | GTCTCTGAAAACCAA[C/G]AGAACTAGCTGTGGT | 51366 |
rs753781720 | snp | C/G | 1.64762e-05 | 0.00287016 | intron-variant | UBR5 | GRCh38.p7 | 8:102268957 | TTTAAACTGAAATGC[C/G]TTCCCAATTGTACAC | 51366 |
rs753783242 | snp | C/T | 1.64855e-05 | 0.00287097 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102278869 | TCCATTAAACATTTC[C/T]CACTACTGGCAGATG | 51366 |
rs753792087 | in-del | -/A | 4.98708e-05 | 0.00499328 | intron-variant | UBR5 | GRCh38.p7 | 8:102293910 | CACTATCACAAAAAC[-/A]GAGTGAAAATGGTAT | 51366 |
rs753857216 | snp | C/T | 1.74756e-05 | 0.00295593 | intron-variant | UBR5 | GRCh38.p7 | 8:102361653 | AACATTAACAAACCA[C/T]GTGTACAGATCTTTT | 51366 |
rs753867920 | snp | A/C | 1.6625e-05 | 0.00288309 | intron-variant | UBR5 | GRCh38.p7 | 8:102270005 | AAAAAAATAACACAG[A/C]CAGTTAAGAGGTAAC | 51366 |
rs753873226 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102323721 | CCTGTTATCCCAGCA[C/T]TTTGGGAGGCCAAGG | 51366 |
rs753899064 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102302810 | TGGACTTCCTACTGC[C/T]CGGCGTGGATAATAA | 51366 |
rs753899373 | snp | A/G | 0.000310672 | 0.0124595 | intron-variant | UBR5 | GRCh38.p7 | 8:102345361 | ATACAGCTAGCCTGT[A/G]ACCAAAATAAATATA | 51366 |
rs753908067 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102406028 | ACCCTGACCTTTCCT[A/C]ATTTCACCTATTATT | 51366 |
rs753915191 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102364380 | AGAGACAGCGTTTTA[A/G]CACGTTGCCCAGGCT | 51366 |
rs753973526 | snp | C/T | 1.64879e-05 | 0.00287118 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295469 | TCGAGGTGGCCTGTA[C/T]TGACAATGCTCCACC | 51366 |
rs753984275 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102290288 | TGCACTGACAGGTTC[C/T]TTCCTATCTCAGTTG | 51366 |
rs753987469 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102268715 | TTGCCAGGAGGGTAT[C/T]CTGATAAGTGAATTT | 51366 |
rs753988129 | snp | C/T | 1.65348e-05 | 0.00287526 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102323411 | TCCAAACTGACTCCA[C/T]TAAGACACCAACTTT | 51366 |
rs753988876 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102405739 | CAGCAGAATCGCTTG[A/T]ACCCGGGAGGCGGAG | 51366 |
rs753999334 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102333234 | AAATTTACTGTATGT[A/C]AATACAAAACAATCA | 51366 |
rs754012689 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102393015 | CAAATAGATAAAATG[A/T]ATGAAGATTAAACGC | 51366 |
rs754015768 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102366658 | AAGGAAAAAAACACT[-/A]AGTAACTCAATAATC | 51366 |
rs754019863 | snp | C/T | 4.94205e-05 | 0.0049707 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102288206 | CAGCATTTTCTTCCC[C/T]GTGTTCTTCCTGTTC | 51366 |
rs754028544 | in-del | -/A | 1.65334e-05 | 0.00287514 | intron-variant | UBR5 | GRCh38.p7 | 8:102360538 | ACACAGGTTTAATAT[-/A]AATACCTAAGAGCTA | 51366 |
rs754050096 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102338227 | AAGAAAGTTGATGTT[C/T]TGGGGTAAAAACCTT | 51366 |
rs754057821 | snp | A/G | 2.39633e-05 | 0.00346137 | intron-variant | UBR5 | GRCh38.p7 | 8:102257758 | TATACTATACCAGTT[A/G]TTGTTATTATCTGTA | 51366 |
rs754064392 | snp | A/G | 4.95176e-05 | 0.00497558 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102259040 | CACATTGACTTCACC[A/G]CAGCCATTTACCAAA | 51366 |
rs754071757 | in-del | -/ACTT | | | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102252947 | GTCACTTCATTGAAG[-/ACTT]ACTTAAGGAAGAAAA | 51366 |
rs754072694 | snp | A/T | | | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303886 | ACCTTAAACTCTAAT[A/T]TGTTATCAGATTATT | 51366 |
rs754073586 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102407600 | AAACCCCATCTCTAC[C/T]AAAAATACAAAAATT | 51366 |
rs754096254 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102352675 | ACCATTTTTTTCCAC[A/G]AGCAAGTACTATTAC | 51366 |
rs754097574 | in-del | -/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102277687 | ACCAGCCTTACCCAC[-/C]CCCCCTCCTTTAAAT | 51366 |
rs754105972 | snp | A/G | 1.6477e-05 | 0.00287024 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102281434 | AATGCTCATCATTAT[A/G]AGACCGCATTAGAGA | 51366 |
rs754107987 | snp | C/T | 1.64803e-05 | 0.00287052 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102288260 | CCACACCCTCCACCA[C/T]CTCAACCTAAATCCA | 51366 |
rs754109686 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102257572 | CTTAAAAGGCCATCA[C/T]ACATGGTATTTTTAA | 51366 |
rs754113503 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102387890 | AGAACTTATTCCTTC[C/G]CCTCTGTTAGACCTA | 51366 |
rs754113647 | snp | C/T | 1.6501e-05 | 0.00287232 | intron-variant | UBR5 | GRCh38.p7 | 8:102275696 | GGAATTTAAGGTGCA[C/T]AAAATACATACTGAT | 51366 |
rs754128024 | snp | C/T | 6.7769e-05 | 0.00582065 | intron-variant | UBR5 | GRCh38.p7 | 8:102281547 | AAAGGAAAATGTTTA[C/T]TAGAAGAATACAAAT | 51366 |
rs754138485 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102398931 | AAACAACTCTACAAG[-/A]AAAAAATCTAATAAT | 51366 |
rs754171505 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102275999 | ATAGCTACTTGTTCC[C/T]GACAACTTATTATTT | 51366 |
rs754206769 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102356948 | AATCATCAATAAATG[C/T]TAAACTCAGTGAGCA | 51366 |
rs754211703 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102363835 | CTAAAGTAAGCTTCG[A/C]GGATATGAGAATGCT | 51366 |
rs754216140 | snp | A/T | 1.71211e-05 | 0.00292579 | intron-variant | UBR5 | GRCh38.p7 | 8:102285112 | GACGTTCTGTATATA[A/T]GAAGAATTTCATACC | 51366 |
rs754228572 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102372413 | GAGGTAAGTTTCATC[C/T]GTTGGCTTCTTGAAT | 51366 |
rs754254168 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102339464 | AACACAGGAGGCAGA[A/G]GTTGCAATGAGCCGA | 51366 |
rs754270813 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102310930 | AGTACTTTCTCCCAA[C/T]TTATTAATAAGATTC | 51366 |
rs754273728 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102401579 | CTGACCTGCAAACCA[C/T]GGCCTGCCAACCTAC | 51366 |
rs754277730 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102264831 | CTCCTACGCCAGCCT[C/T]CCAAGTAGCTGGGAC | 51366 |
rs754281973 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102277311 | TTTCTGGAGCTTCAA[C/T]GGTCCTTTTGTCTGA | 51366 |
rs754282815 | snp | A/G | 2.20583e-05 | 0.00332094 | missense, nc-transcript-variant, intron-variant | UBR5 | GRCh38.p7 | 8:102264511 | ATTACATGTCTATTC[A/G]ATGTGATAGGACATA | 51366 |
rs754284719 | snp | C/G | 0.000165289 | 0.00908941 | intron-variant | UBR5 | GRCh38.p7 | 8:102360548 | TAATATAATACCTAA[C/G]AGCTAAATACATATT | 51366 |
rs754290017 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102388714 | AGTAAAGAACTAATC[A/G]CTAGCTCACATTTCA | 51366 |
rs754293400 | in-del | -/A | 1.68241e-05 | 0.00290031 | intron-variant | UBR5 | GRCh38.p7 | 8:102261278 | GAAAAATTTACCAGT[-/A]GCTATTTAAAGGCAA | 51366 |
rs754303219 | snp | G/T | 1.66214e-05 | 0.00288278 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102294084 | TTGTTTTGGAGTTCT[G/T]TCACTAGTGTACCTA | 51366 |
rs754312352 | snp | C/T | 3.2956e-05 | 0.00405918 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102329110 | TATTTTCTGTAGCTA[C/T]AGTTGCTCTTATGCT | 51366 |
rs754350800 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102293518 | ATCATGTACACCACC[C/T]GAGTGCTTATGCAAA | 51366 |
rs754361526 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102400433 | CCGAAGTTTCAGGAC[A/G]GTTTGGTGTGGCAAT | 51366 |
rs754364669 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102328772 | TTTTGTATTTTTAGT[A/T]GAGATGGGGTTTTGT | 51366 |
rs754367406 | snp | C/T | 1.66101e-05 | 0.0028818 | intron-variant | UBR5 | GRCh38.p7 | 8:102312316 | AGTTCCAATATTCAC[C/T]TGCTGAATAACTTCT | 51366 |
rs754367540 | snp | A/G | 4.95749e-05 | 0.00497845 | intron-variant | UBR5 | GRCh38.p7 | 8:102329227 | TAAAAAAAAATTACT[A/G]TTTTATATGTTGATA | 51366 |
rs754367974 | in-del | -/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102409635 | AGTCAAGCTACAGTA[-/G]GCAGTAGCTTTTTTA | 51366 |
rs754389068 | snp | C/T | 6.59217e-05 | 0.00574078 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102286440 | GCCCACTGCATTGAA[C/T]GGGGAGCTTGGGCAG | 51366 |
rs754392306 | snp | C/T | 1.65754e-05 | 0.00287879 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295029 | AATGAGTGAAACAGT[C/T]CAGCCGAATTGTGCC | 51366 |
rs754434436 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102297828 | CATATGATGCCAATA[C/T]AAACACACTATACAT | 51366 |
rs754437831 | snp | A/C | 0.000169512 | 0.00920473 | intron-variant | UBR5 | GRCh38.p7 | 8:102265093 | CCCAAGATTAAAGTT[A/C]TTTTACCTGCCAATG | 51366 |
rs754450314 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102283555 | CCACCAATCAAGATC[C/T]GCTATCAGAATTCTG | 51366 |
rs754453491 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102333667 | TATTCCTGAATTTTG[A/C]CCCACAAAACTTGGT | 51366 |
rs754455431 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102309817 | ATTAAGCAACACATG[A/T]CTACGTAACTAGAAT | 51366 |
rs754455941 | snp | A/G | 0.000230974 | 0.010744 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102412124 | GGGGGAGGGGAGGGA[A/G]GGAAGGGCGCCCCTC | 51366 |
rs754485495 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102285876 | AATCTAAATGGTCAA[C/T]TGTGGTACCCAAGCA | 51366 |
rs754518652 | snp | A/T | 4.37249e-05 | 0.00467553 | intron-variant | UBR5 | GRCh38.p7 | 8:102286311 | TGAACATGCATAATT[A/T]AAAAAATCTATCTAA | 51366 |
rs754523282 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102296789 | CGTAAGTAACCTCAT[A/G]CTTTCTGAAGTAAAA | 51366 |
rs754539267 | snp | C/T | 1.65067e-05 | 0.00287282 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102278935 | TCCTCCTTTCTAGCA[C/T]TTGGCTGGAATTTTA | 51366 |
rs754540269 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102345784 | TATAACACTTGTGGC[C/T]GGGCACGGTGGCTCA | 51366 |
rs754554117 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102263667 | TACTTCTTACATTCT[C/T]TGGCCACCCCCATGT | 51366 |
rs754562275 | snp | A/G | 1.65965e-05 | 0.00288062 | missense, utr-variant-5-prime, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102300141 | GTCTCATCATTTCCC[A/G]TAATCTCAAACTAAA | 51366 |
rs754592588 | in-del | -/CACATATA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102396663 | ATACACACACACACA[-/CACATATA]TATATATATACACAC | 51366 |
rs754608948 | snp | A/G | 1.65636e-05 | 0.00287776 | intron-variant | UBR5 | GRCh38.p7 | 8:102270031 | GTAACTAAGTACACA[A/G]TACACACTGGTTGCA | 51366 |
rs754612244 | snp | A/T | 1.66879e-05 | 0.00288855 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102304025 | CCAATTAAAGTTTCC[A/T]GGTAAAAATCACATT | 51366 |
rs754613296 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102375766 | AGGAGAGCTTATCAG[C/G]AAGCAAAATTACAGA | 51366 |
rs754624808 | snp | C/T | 1.65323e-05 | 0.00287505 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102279198 | ATCATCCTTATCATT[C/T]AAAGTAGCACCTAAA | 51366 |
rs754656404 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102347200 | ATCTGTCTAATTGAC[A/C]TAACATGTTACATAG | 51366 |
rs754673930 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102365777 | ACAGAGACAGGAAAA[C/T]AGTGTAACGGTACTT | 51366 |
rs754680378 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102287980 | GAAACTATTTTATAT[A/G]TGTATTATATATAGC | 51366 |
rs754714370 | snp | C/T | 1.68721e-05 | 0.00290444 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102323482 | TGATAAAGAGGATTA[C/T]TTCTCAAGCATACCT | 51366 |
rs754777266 | snp | C/T | 1.64773e-05 | 0.00287026 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102289548 | GCTGTGGATTCCTGA[C/T]GATGTAGGATGACTG | 51366 |
rs754782701 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102305555 | TTCTCAACTAACTCA[C/G]CTCTGCAACTGAAAC | 51366 |
rs754789780 | in-del | -/AG | | | intron-variant | UBR5 | GRCh38.p7 | 8:102361447 | GCCCAACCCATAAAA[-/AG]AGTTGACAGATTAAA | 51366 |
rs754814280 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102340981 | GTATACTTAAAAACA[C/T]ATCTATCATATTTTT | 51366 |
rs754828421 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102265499 | TTTAACGTCTCTGTT[A/G]TTAAAATAAAGTCAT | 51366 |
rs754834938 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102306409 | CCAACTTGAGAGCGG[A/G]TGGAGAACAGATGTC | 51366 |
rs754842037 | snp | C/G | 1.65102e-05 | 0.00287312 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102326548 | ATCCATCACTTACCT[C/G]GGTACCAACAGTGAT | 51366 |
rs754859971 | snp | G/T | 1.65853e-05 | 0.00287964 | intron-variant | UBR5 | GRCh38.p7 | 8:102311524 | GAAAATGGTAAAGTT[G/T]GACTCCTAATCAAAA | 51366 |
rs754867954 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102328609 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCACTGT | 51366 |
rs754881128 | snp | A/G | 1.70892e-05 | 0.00292306 | intron-variant | UBR5 | GRCh38.p7 | 8:102261127 | ATTGGATCACACAAC[A/G]CTTTCTAGAAACACT | 51366 |
rs754897823 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102384986 | TTGAATGATGGCAAG[A/G]TTTACTTAAGACATT | 51366 |
rs754901186 | snp | G/T | 1.65261e-05 | 0.0028745 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285157 | GTTCGTAAGCTAGCT[G/T]CTTCTCGCGCAGTCA | 51366 |
rs754901399 | in-del | -/AAAG | | | intron-variant | UBR5 | GRCh38.p7 | 8:102284276 | TGTGATTTGAGAAAA[-/AAAG]AGCAGCACTGGTAAT | 51366 |
rs754930293 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102292487 | AGTTTCAAGGGCAGT[C/G]TTTAGAGATGAGACG | 51366 |
rs754944061 | snp | C/G | 8.52072e-05 | 0.00652659 | intron-variant | UBR5 | GRCh38.p7 | 8:102265285 | GTTTTCCTGCTAACA[C/G]AGAATATCAGAGAGT | 51366 |
rs754971736 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102331820 | TCCACCTACCTTCCA[-/T]TCTCCCTGGCACTAC | 51366 |
rs754973775 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102340083 | AATCACCACCTGTCT[C/T]CTGCACTAAACCTCA | 51366 |
rs754987178 | snp | C/T | 3.36168e-05 | 0.00409967 | intron-variant | UBR5 | GRCh38.p7 | 8:102285354 | CTATGAAGACCAAAC[C/T]AAAATAGTTAAAACT | 51366 |
rs754993422 | snp | C/G | 1.66313e-05 | 0.00288364 | intron-variant | UBR5 | GRCh38.p7 | 8:102360709 | TCCAAGTAAAAATGT[C/G]TATTAAAATTTGAAT | 51366 |
rs754997878 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102353771 | AACCATAGGCTGGGT[C/T]CACGCCTGTAATTCC | 51366 |
rs755010294 | in-del | -/CAAAAT | 4.98269e-05 | 0.00499109 | intron-variant | UBR5 | GRCh38.p7 | 8:102293932 | AAATGGTATCTAAAC[-/CAAAAT]CAAAAAGGATGCCTT | 51366 |
rs755012695 | snp | C/G | 3.30202e-05 | 0.00406313 | intron-variant | UBR5 | GRCh38.p7 | 8:102360569 | AATACATATTAAATA[C/G]AAAGGACATAATATC | 51366 |
rs755024025 | in-del | -/TGTG | | | intron-variant | UBR5 | GRCh38.p7 | 8:102279441 | GCAAATTTTACGTTA[-/TGTG]TATGTTACAATAAAA | 51366 |
rs755025577 | snp | A/G | 1.65042e-05 | 0.0028726 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102329310 | GTAAGGCTCAGATTC[A/G]CTCCATTTCCACTGA | 51366 |
rs755025703 | snp | C/T | 1.64855e-05 | 0.00287097 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311338 | AGCTTTCTTTTTGAT[C/T]GTTGAATTGGCAGGA | 51366 |
rs755038880 | snp | A/C | 1.66835e-05 | 0.00288816 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102298852 | AATCCTCTTACTTGG[A/C]AGAAAGAAGTTCTCG | 51366 |
rs755042786 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102402171 | CAGTGAGCCAATATT[A/G]CATCACTGCACTCCA | 51366 |
rs755051051 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303813 | TAGAACAAATTGAAA[C/G]AAACAAATTTAAACT | 51366 |
rs755066963 | snp | A/C | 1.65345e-05 | 0.00287524 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295109 | CTACTGCTGGCACTA[A/C]GACTTGAGGAGAAAC | 51366 |
rs755077368 | snp | A/G | 0.000462611 | 0.0152017 | intron-variant | UBR5 | GRCh38.p7 | 8:102329242 | ATTTTATATGTTGAT[A/G]TGTAGAGCTATTCAA | 51366 |
rs755079248 | snp | C/T | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102277032 | TCTGCTAGTAAGCTA[C/T]TTTTTAATTGTGCAG | 51366 |
rs755103231 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102342351 | CAAAAATATTGTTTT[A/C]TATATTTGTGTTTTT | 51366 |
rs755134181 | snp | G/T | | | utr-variant-3-prime | UBR5 | GRCh38.p7 | 8:102253349 | AATATTACTTGACAT[G/T]TCTTCTGTAATTTCT | 51366 |
rs755146286 | snp | A/G | 1.65866e-05 | 0.00287976 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102312213 | CCTTTGGAAACAGTC[A/G]GGAACCTTCGGTGTT | 51366 |
rs755150008 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102299234 | CAAATAATTTAAACC[C/T]ATGAACACCATTTTA | 51366 |
rs755163809 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102349002 | TTCTGTACTTGCTGA[A/T]GCACACTACCAATTC | 51366 |
rs755177570 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102280254 | TAAGCAAAAATGGAC[A/G]GAAAATGTAAGAAAT | 51366 |
rs755187384 | in-del | -/CCC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102315374 | GGATTAAAAAACTAG[-/CCC]TCTTTAATGAGTTAT | 51366 |
rs755192072 | snp | C/T | 1.64936e-05 | 0.00287168 | intron-variant | UBR5 | GRCh38.p7 | 8:102266910 | CCTTGTAATTTAAAT[C/T]CTGTGATTATCAGCA | 51366 |
rs755203782 | in-del | -/ATT | 4.94707e-05 | 0.00497322 | cds-indel, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102360594 | AATATCTTACCCATC[-/ATT]ATTATCAGGTTTACC | 51366 |
rs755205468 | snp | C/T | 1.64735e-05 | 0.00286993 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102313843 | ATCTTCCACAAAAAC[C/T]ACTTCCCGAAGAGAC | 51366 |
rs755227844 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102344569 | ACCTCGTGATCCACC[C/T]ACCTTGGCCTCCCAA | 51366 |
rs755245964 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102266759 | CTGAGCCCTAATTAA[G/T]CCAAGCTTATTATTT | 51366 |
rs755254159 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102361484 | TTAAAGTCTAATAAT[C/T]ACATTAATCTTAATC | 51366 |
rs755259004 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102379883 | TGAGATACAAGATGA[G/T]TATCTCCACACAAGA | 51366 |
rs755265256 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102319141 | AAGACACAGACTGGC[-/A]AAATTGGATAAACAG | 51366 |
rs755284360 | snp | A/G | 9.90164e-05 | 0.00703551 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102254383 | GGAATAGAGTGGGAC[A/G]TAAAGTCGAGAAATG | 51366 |
rs755294698 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102390989 | ACAATTTGGGAGGCC[A/G]AGGCGGGAGAATCCC | 51366 |
rs755308461 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102403177 | ATTTTGGGAGGCCAA[A/G]GTGGGAAGACAGCTT | 51366 |
rs755331927 | in-del | -/A | 7.84929e-05 | 0.00626421 | intron-variant | UBR5 | GRCh38.p7 | 8:102327926 | ATTAGAACTTTAAAT[-/A]AAATCAAGCCATCTT | 51366 |
rs755332022 | snp | A/G | 5.41971e-05 | 0.00520535 | intron-variant | UBR5 | GRCh38.p7 | 8:102314703 | CACAGCTGTCTGCAT[A/G]AGACCTATTTTCACA | 51366 |
rs755336910 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102267547 | TTGATTTTTCTATAA[C/T]GGACTAAGCTATACC | 51366 |
rs755338105 | snp | A/G | 1.66374e-05 | 0.00288417 | intron-variant | UBR5 | GRCh38.p7 | 8:102281275 | TAAATCAACCTCATG[A/G]CAAGAATGGATACCT | 51366 |
rs755344417 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102300681 | TACACACAAAAAAAT[C/T]TTTAACAGTACAACT | 51366 |
rs755352283 | snp | A/G | 1.64836e-05 | 0.0028708 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102287449 | TGCTTCTGAACCAGC[A/G]GTTGCTGCAGTGACA | 51366 |
rs755357281 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102350566 | ATTATATACAAAAAT[G/T]AACAAAAAATGAATT | 51366 |
rs755362196 | snp | C/T | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102305156 | TGCAAAATATTTCGA[C/T]TTCCATCACATCTGT | 51366 |
rs755388544 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102402333 | TTTGTAGAGGCAGAT[G/T]ATGTTACAGAGCAAT | 51366 |
rs755407241 | snp | C/T | | | utr-variant-3-prime | UBR5 | GRCh38.p7 | 8:102252804 | TTCTGAAGGAAGTTA[C/T]ATAATAAAAGCATAG | 51366 |
rs755417323 | snp | C/T | 1.672e-05 | 0.00289132 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295770 | GTAGGCTGTTGGTGA[C/T]GTCCGTTTGAGTCTA | 51366 |
rs755420437 | snp | C/G/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102412709 | CACTTCTGCCCCAGT[C/G/T]TCTCCGTCTCGCAGG | 51366 |
rs755426233 | in-del | -/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102312031 | GTTACAGATAGGGAA[-/C]AAAAAAATGCCAATG | 51366 |
rs755429009 | in-del | -/AT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102396640 | TATATATATACACAC[-/AT]ATATATATACACACA | 51366 |
rs755440869 | snp | C/T | 3.43619e-05 | 0.00414485 | intron-variant | UBR5 | GRCh38.p7 | 8:102326713 | AGTAAAACAGCCCAC[C/T]AAATAAATCTGAAAT | 51366 |
rs755445630 | snp | A/T | 3.70357e-05 | 0.00430308 | intron-variant | UBR5 | GRCh38.p7 | 8:102257595 | ATTTTTAACTTCTGT[A/T]TTTCCTTCTACAAAT | 51366 |
rs755449780 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102335883 | TTTCATCTCCTCTGG[A/G]TACGTACATAATAGG | 51366 |
rs755467466 | snp | C/T | 8.35834e-05 | 0.00646411 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102296950 | CAACAACACAGTGAC[C/T]CCAGCAAGCCACAAG | 51366 |
rs755469442 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102272958 | TAAAGCATACAAGAA[A/T]GTCTTGCAAATTAAA | 51366 |
rs755488966 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102397660 | GAGCCGAGATTGCCA[C/T]TGCACTCCACCCTGG | 51366 |
rs755491689 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102368505 | GTAAGCATAGCTCAC[C/T]GCAGCCTCAAACTCC | 51366 |
rs755492756 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102325456 | TGTCTAAGTTTTAAG[A/G]ATTAAGTTTTTAAAC | 51366 |
rs755496800 | snp | C/T | 1.65023e-05 | 0.00287244 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102347041 | AGCTCCAGCTGATGA[C/T]CTACCAGAGGATCCT | 51366 |
rs755506207 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102369837 | GAATACAATGACAAT[C/T]AGTTGTACAGTTTGG | 51366 |
rs755517301 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102288053 | AAATAAGTTTGACCA[C/T]TTCACTATACATTCA | 51366 |
rs755544757 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102293546 | AAAGGTTTTAGGAAG[C/T]CAAACACGACATTTC | 51366 |
rs755545129 | in-del | -/T | 1.69229e-05 | 0.00290881 | intron-variant | UBR5 | GRCh38.p7 | 8:102261294 | GCTATTTAAAGGCAA[-/T]TTTGTCAAAGCAGTA | 51366 |
rs755550646 | snp | A/T | 3.30961e-05 | 0.0040678 | intron-variant | UBR5 | GRCh38.p7 | 8:102360040 | ATACAGACCATCTGT[A/T]AGATGGTGCCTTCAA | 51366 |
rs755551963 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102335769 | GGCCAGATTGGTCTC[A/G]AACTCCTGACCTCAG | 51366 |
rs755554165 | snp | C/T | 1.65822e-05 | 0.00287938 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102279208 | TCATTCAAAGTAGCA[C/T]CTAAACATAAAAAGA | 51366 |
rs755578911 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102378941 | TGCATGGATATGACA[C/G]TAAGAGAGCTAATCT | 51366 |
rs755583827 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102270439 | ACACATAATTCTGGA[A/C]ATTTTAGTCAAAAGT | 51366 |
rs755593517 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102316332 | CCCTATCGTTTTTCA[A/C]TGCCTGAATACATTT | 51366 |
rs755599339 | snp | G/T | 3.34835e-05 | 0.00409153 | intron-variant | UBR5 | GRCh38.p7 | 8:102346218 | GAAATGAGAAAAACA[G/T]GACGGTGATCCACCA | 51366 |
rs755614750 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102407874 | TCCTTAACCTTAGCA[C/T]AACTGACATTTTGGA | 51366 |
rs755619443 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102285410 | AGCAGCAGTATGTCA[A/G]TATGTAAACGTTTCT | 51366 |
rs755625252 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102315025 | AGACTCAAGAATAAA[A/G]GGTACACAATGCATG | 51366 |
rs755628519 | snp | A/G | 1.65007e-05 | 0.00287229 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102286565 | ATCAGAATCACTTGA[A/G]TCATTCGATTGAGAA | 51366 |
rs755652672 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102380384 | ACAAAGCTAGACTCA[-/A]AAAAAAAAAAAAAAC | 51366 |
rs755680852 | snp | A/C | 1.65378e-05 | 0.00287552 | missense, upstream-variant-2KB, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102304132 | CTCAACAGCAGAAAG[A/C]CTTTCTGCAAATGTA | 51366 |
rs755692010 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102366128 | TCACATACTCTACAA[A/G]GTGATGGTTTCCATA | 51366 |
rs755702939 | in-del | -/ATC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102335385 | AGTTAATAAAATGGT[-/ATC]ATATTATGGATTTTT | 51366 |
rs755713792 | snp | C/T | 1.75721e-05 | 0.00296407 | intron-variant | UBR5 | GRCh38.p7 | 8:102346860 | TCAGTAAAACCTCAC[C/T]TTGTCCTGTTGTCTG | 51366 |
rs755715776 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102305633 | TCGGCCTTTGGGCCA[C/T]AGTCTGCCAATCCTT | 51366 |
rs755733403 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102367049 | AAGTCTTGGAGTGGT[C/G]GTCTTGCCTATACCA | 51366 |
rs755753791 | snp | C/T | 1.65679e-05 | 0.00287814 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295696 | TAAAGTAGATCAAGA[C/T]GAGCAGATTTCTGTC | 51366 |
rs755756123 | snp | A/G | 1.66385e-05 | 0.00288426 | intron-variant | UBR5 | GRCh38.p7 | 8:102271121 | GGTATTGAATCAAAG[A/G]TACAAAATTTACCTA | 51366 |
rs755766897 | in-del | -/ACAAAGAGGG | | | intron-variant | UBR5 | GRCh38.p7 | 8:102355788 | AGAGAGAACAGAGGC[-/ACAAAGAGGG]GTTTACGGGGAGTGT | 51366 |
rs755772633 | snp | C/T | 0.000148826 | 0.008625 | intron-variant | UBR5 | GRCh38.p7 | 8:102272514 | TAAGCTGCTTGTTAT[C/T]TGTAGAGTACTTACT | 51366 |
rs755773521 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102265680 | TATAGGTAAAGAACC[A/G]TTCTTTGGCTGCTTT | 51366 |
rs755778221 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102395188 | CTTCAGGTAAGCTTT[C/T]CCCCTGCCCAAGACT | 51366 |
rs755799625 | in-del | -/AAAGACCTTAATGGTA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102331000 | GAAGATAATGAGAAT[-/AAAGACCTTAATGGTA]AAAGACCTTAATGGT | 51366 |
rs755823839 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102353899 | AGCTGGGCATGGTGG[C/T]GCATGCCTGTAGTCC | 51366 |
rs755828825 | snp | A/G | 1.64773e-05 | 0.00287026 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102289552 | TGGATTCCTGATGAT[A/G]TAGGATGACTGAGAC | 51366 |
rs755847718 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102332134 | GGAGACACGACAATC[A/G]AATTGACTGATGAGA | 51366 |
rs755858964 | snp | A/G | 1.65507e-05 | 0.00287664 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102261174 | TCTGCAACTACCAAC[A/G]TTCTGTGTTCTGCGT | 51366 |
rs755885720 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102408582 | GCATCTTGAGGAATA[A/G]TTCAGGACAAGGACA | 51366 |
rs755890167 | snp | C/T | 3.30262e-05 | 0.0040635 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285178 | CGCGCAGTCATCCTC[C/T]CTCTTCTCGCTGAAT | 51366 |
rs755892091 | snp | A/T | 1.69049e-05 | 0.00290726 | intron-variant | UBR5 | GRCh38.p7 | 8:102326695 | TAAATTGGTCAAATA[A/T]GCAGTAAAACAGCCC | 51366 |
rs755903234 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102385058 | GAGCCTAGTACAAAA[C/T]GTTAGCTGCTCCTGC | 51366 |
rs755906322 | snp | A/G | 1.68729e-05 | 0.00290451 | intron-variant | UBR5 | GRCh38.p7 | 8:102285374 | TAGTTAAAACTATCC[A/G]AATAGAGCTAAATTC | 51366 |
rs755910352 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102306544 | CAGCAAGCTCCAGTT[C/T]ATGAGGAGCTTAATA | 51366 |
rs755923518 | in-del | -/CTTC | 1.68023e-05 | 0.00289843 | frameshift-variant, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102293718 | AATGGTGCAGTTGGA[-/CTTC]CGAGCAATCCCCATT | 51366 |
rs755934596 | in-del | -/AC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102396650 | CACACATATATATAT[-/AC]ACACACACACACACA | 51366 |
rs755978380 | snp | C/T | 1.76272e-05 | 0.00296872 | intron-variant | UBR5 | GRCh38.p7 | 8:102311929 | AAAAATTGTTATACA[C/T]CTTATCTCTAATAAA | 51366 |
rs755981360 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102403370 | TGGGCAACACAGAGA[C/G]ACTCCATCTCTACAA | 51366 |
rs755994183 | snp | C/T | 3.29468e-05 | 0.00405861 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102277076 | AGATGGCCCTGGTTT[C/T]GAACTCTCAGTTTCT | 51366 |
rs756005752 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102386157 | AATGGAGACCAGGTG[C/T]AGTGACTCACGCCTG | 51366 |
rs756018289 | snp | A/G | 0.000215355 | 0.0103745 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102298889 | GGGCTGGAGAACCAC[A/G]CTGTCACATAACAAT | 51366 |
rs756024637 | snp | C/T | 1.76871e-05 | 0.00297375 | intron-variant | UBR5 | GRCh38.p7 | 8:102261876 | AGCAGTTTAACCAAA[C/T]TCTCTTGCCAGAATC | 51366 |
rs756029212 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102375508 | ACATTATAATTCAAA[G/T]GGTGCTATAAGAGTA | 51366 |
rs756046296 | snp | C/T | | | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295514 | TGTCTGTACTAAGAA[C/T]AGTAAGAGGTGCTCT | 51366 |
rs756053136 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102392344 | AAAATTTACTGAATC[C/T]AGAAGGTACTATCTA | 51366 |
rs756059177 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102330530 | ACCAAATTTGGAATT[A/C]TCCAAGTTAGCAATT | 51366 |
rs756081811 | snp | A/G | 1.6886e-05 | 0.00290564 | intron-variant | UBR5 | GRCh38.p7 | 8:102329449 | ATTGCCAAATCTACT[A/G]ATTTGAACACTGTCA | 51366 |
rs756087820 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102369061 | AAAAATTTTCCCAAA[A/C]ATATTTGACAAGGGG | 51366 |
rs756103523 | snp | C/T | 1.66286e-05 | 0.0028834 | intron-variant | UBR5 | GRCh38.p7 | 8:102298979 | GGAAGGACCTGTAAT[C/T]AAGCAGATTCATTTG | 51366 |
rs756107929 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102280574 | AAAAAGGTCGCTAAT[A/G]TATCTAACCAATTTC | 51366 |
rs756108024 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102329490 | TTCATCAGATCTAGA[G/T]TAATTATGTAAACAC | 51366 |
rs756126623 | snp | C/T | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102342547 | TCTTCTTATCCAAGT[C/T]TGGCTCTCCTTCCTT | 51366 |
rs756159219 | snp | C/G | 1.65597e-05 | 0.00287743 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102287545 | AGCTGCTGCTAACAA[C/G]TCCAGCTCCATATCA | 51366 |
rs756168058 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102300916 | ATAAAACCTTACAAC[A/G]GCTACAAAATTAATA | 51366 |
rs756172163 | snp | A/C | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102313857 | CCACTTCCCGAAGAG[A/C]CCACTGCTCTTCATT | 51366 |
rs756183671 | snp | A/G | 4.94507e-05 | 0.00497221 | intron-variant | UBR5 | GRCh38.p7 | 8:102266927 | TGTGATTATCAGCAC[A/G]TGAATAAAATGTTCC | 51366 |
rs756194020 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102347474 | AGATGAGGTCTTGCT[A/G]TGTTGCCCAGGCTAG | 51366 |
rs756197695 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102313350 | AAGAGTGAAATTAAT[A/G]GCACTCAAATTGATG | 51366 |
rs756199153 | snp | A/G | 1.65828e-05 | 0.00287943 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295231 | TCCTGCGACCCAAAC[A/G]TAATCATAGATTTCA | 51366 |
rs756210317 | snp | A/C | 1.64792e-05 | 0.00287042 | intron-variant | UBR5 | GRCh38.p7 | 8:102268936 | ACTGAAAGTAAGTAG[A/C]TGATGTTTAAACTGA | 51366 |
rs756218871 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102312333 | GCTGAATAACTTCTT[A/T]ACACTTACCTGCAAT | 51366 |
rs756219975 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102391818 | AGACAGTTAGGCATT[C/G]TAAGTCACAGGATGA | 51366 |
rs756220525 | snp | A/G | 1.6679e-05 | 0.00288777 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102257653 | TTGTCGTTCTGTCAT[A/G]CTCATCTTCTCTACT | 51366 |
rs756220806 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102402584 | TTAAGGCTTAAAAAA[C/T]CATCTTCCTCCACTT | 51366 |
rs756225174 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102362617 | CAGACAAAAATGTTA[C/T]ACATACTCCAAAAAT | 51366 |
rs756279570 | snp | A/G | 1.64893e-05 | 0.0028713 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102254410 | AATGCAAGTATTTGC[A/G]GTAGGAAGATGTTGG | 51366 |
rs756290784 | snp | C/G | 1.75486e-05 | 0.0029621 | intron-variant | UBR5 | GRCh38.p7 | 8:102314722 | CCTATTTTCACAAAT[C/G]CATACAACAAATAAA | 51366 |
rs756309762 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102267045 | ATTCCAGATAACGGA[A/G]ACTTCTAGAATTTAG | 51366 |
rs756321840 | snp | A/G | 1.65288e-05 | 0.00287474 | intron-variant | UBR5 | GRCh38.p7 | 8:102295362 | ATAGTGACCAAAACA[A/G]AAATAAAACATATTG | 51366 |
rs756322286 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102302673 | GTATTCCATTCAATA[C/T]TGAAATTGCATCAGT | 51366 |
rs756344146 | snp | C/T | 3.29511e-05 | 0.00405887 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102305258 | TGTCGACAGGCCTCA[C/T]AGTCACAGCGCAGAA | 51366 |
rs756360119 | snp | A/G | 8.32771e-05 | 0.00645226 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102323458 | ATTGAAAATGCAACT[A/G]CTCCAGCATGATAAA | 51366 |
rs756379895 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102350747 | TCAAAGGACACAATC[A/G]ACAGACAACCTACAG | 51366 |
rs756409477 | snp | A/C/G | 4.9489e-05 | 0.00497414 | missense, synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295516 | TCTGTACTAAGAATA[A/C/G]TAAGAGGTGCTCTCC | 51366 |
rs756412138 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102379957 | TAGAAGCCAGTTAGG[C/T]CCACATTTTTAGTAG | 51366 |
rs756442143 | in-del | -/TT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102406936 | TGTGCAAAAACACAC[-/TT]TTTCTATGCCAACAC | 51366 |
rs756466704 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102290129 | CAGTTGACTGGATTA[C/T]AAAACAAAAAGGGGG | 51366 |
rs756470531 | in-del | -/AA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102300283 | AGGGAAGTGAAGTAC[-/AA]AAATGCCAATTCTGG | 51366 |
rs756478000 | snp | A/T | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102281421 | GGAAGAACATCAGAA[A/T]GCTCATCATTATGAG | 51366 |
rs756486696 | snp | A/G | 1.65318e-05 | 0.002875 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102297538 | AAGGAGAGTCATCAG[A/G]GTTGGTACCTGATGG | 51366 |
rs756500480 | snp | A/G | 1.73748e-05 | 0.00294739 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102296979 | AGTTCGACACTCAAA[A/G]ATATCCTAAAATTAA | 51366 |
rs756517212 | snp | A/C | 1.65081e-05 | 0.00287293 | intron-variant | UBR5 | GRCh38.p7 | 8:102275663 | TATTCCCTGAAATAC[A/C]TGCTTATCAGGCAGA | 51366 |
rs756520520 | snp | C/T | 1.68758e-05 | 0.00290476 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102293790 | TTCCACAGCGTAAGG[C/T]AGCAATGCTTGGAAT | 51366 |
rs756527799 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102289083 | GGCAGGAGAATCGCT[C/T]GAACCCGGGAGGCAG | 51366 |
rs756563814 | snp | A/C/T | 3.41812e-05 | 0.00413396 | intron-variant, splice-donor-variant | UBR5 | GRCh38.p7 | 8:102275514 | AAGAAAATCTAAATA[A/C/T]CTTTACCTCTAGTGA | 51366 |
rs756590838 | snp | C/T | 1.66029e-05 | 0.00288117 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102312242 | TTCCACCAGTTTTGA[C/T]AACCTGCATGACACA | 51366 |
rs756598732 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102262381 | ATTATGGGGAGCAGC[C/T]GGCTCTGAACTTAAT | 51366 |
rs756601127 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102356189 | GCGCGGTGGCTGACA[C/T]CTGTAATCCTAGCAC | 51366 |
rs756617105 | snp | A/T | 8.28933e-05 | 0.00643737 | intron-variant | UBR5 | GRCh38.p7 | 8:102293947 | CAAAATCAAAAAGGA[A/T]GCCTTACTTTTTCTT | 51366 |
rs756623071 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102387946 | CTCACATCCTTGTCT[C/T]ATGAGTAACAAGAAG | 51366 |
rs756648913 | snp | C/T | 1.64838e-05 | 0.00287083 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102327815 | AAACTATCCGCTCTC[C/T]TTGAAGTTCAGAGTA | 51366 |
rs756668652 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102370848 | CATAGCTCCCACATA[C/T]GAATGAGAACATGCA | 51366 |
rs756692258 | snp | C/G/T | 0.000263683 | 0.0114797 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102272546 | GTGTGGGTGCCTTTG[C/G/T]TGGCATTTTGGATAC | 51366 |
rs756702040 | snp | A/G | 0.000362486 | 0.0134578 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102329105 | CTTGTTATTTTCTGT[A/G]GCTACAGTTGCTCTT | 51366 |
rs756731958 | snp | C/T | 1.69545e-05 | 0.00291152 | intron-variant | UBR5 | GRCh38.p7 | 8:102281242 | TACTAAAGAAGACCA[C/T]ACCAAGCAAGTATTT | 51366 |
rs756759124 | in-del | -/GAC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102266020 | ATCTTCAAGCTGACT[-/GAC]ACTTTCCTCCAACAC | 51366 |
rs756761218 | snp | A/G | 3.32193e-05 | 0.00407536 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295746 | TTTACATTTCTCCCA[A/G]CAATCACAGTAGGCT | 51366 |
rs756763633 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102396880 | CCAGCAAATTTTTTT[A/G]TATTTTTAGTAGAGA | 51366 |
rs756765103 | snp | C/G | 1.64822e-05 | 0.00287068 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102347006 | GTCCGAATAACTCGA[C/G]TCTGCCGGCGGGAAT | 51366 |
rs756770222 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102386507 | ATCAAACCCCATGCA[A/G]AAGGGAAGAAAAGAT | 51366 |
rs756772063 | in-del | -/GGGGGT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102283351 | AAGGCGGGGGGGGGG[-/GGGGGT]GGGGGTGAGTAGGGG | 51366 |
rs756797139 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102368406 | CTTTCTAGCTCTTTA[C/T]AGGAGGGTTTTCTGT | 51366 |
rs756805741 | snp | A/C | 1.67522e-05 | 0.0028941 | intron-variant | UBR5 | GRCh38.p7 | 8:102293599 | TGTTACCTGGTAGCA[A/C]TTTACCTGCTAGACT | 51366 |
rs756817945 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102408795 | TCTGAGACAGCAGAA[A/C]CATTCTGGAATACAA | 51366 |
rs756824972 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102272841 | GCTTGAATTTTTCTA[C/T]GTACAATCTGAAAAT | 51366 |
rs756852623 | snp | C/T | 1.64868e-05 | 0.00287109 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102272688 | CTCTGTGTACAGCCA[C/T]TGGTGTAGTAGCACA | 51366 |
rs756855045 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102317261 | GCTTTTCTGACGGGC[A/T]TAGGAAATGGCACAC | 51366 |
rs756862511 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102307466 | TGTCTAAATAAAAGC[C/T]TACAGATAGTGCTCA | 51366 |
rs756866790 | snp | C/G | 3.40437e-05 | 0.00412561 | intron-variant | UBR5 | GRCh38.p7 | 8:102326705 | AAATAAGCAGTAAAA[C/G]AGCCCACTAAATAAA | 51366 |
rs756874485 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102260756 | ATTTTAAAATATAAA[A/G]ACAATTCTTTATCTG | 51366 |
rs756878323 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102354945 | ACCAGCCTGGGCAAC[A/G]TGGCAAAACCCTGCT | 51366 |
rs756879954 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102271655 | ATATTACCTATTATT[A/G]TTTTTAAATTCCTAA | 51366 |
rs756895761 | snp | C/G | 1.68832e-05 | 0.00290539 | intron-variant | UBR5 | GRCh38.p7 | 8:102285379 | AAAACTATCCAAATA[C/G]AGCTAAATTCGATAC | 51366 |
rs756904388 | snp | C/T | 3.50447e-05 | 0.00418582 | intron-variant | UBR5 | GRCh38.p7 | 8:102261899 | CCAGAATCAGAAAAG[C/T]GTATATTTGCTTTAC | 51366 |
rs756919712 | snp | C/T | 1.80945e-05 | 0.00300781 | intron-variant | UBR5 | GRCh38.p7 | 8:102311935 | TGTTATACATCTTAT[C/T]TCTAATAAACATCTA | 51366 |
rs756945456 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102386212 | AGGCGGGTGGATCAC[C/T]TGAGGTCAGGAGCTT | 51366 |
rs756975765 | in-del | -/TAAT | 3.43581e-05 | 0.00414462 | intron-variant | UBR5 | GRCh38.p7 | 8:102277238 | TGAAGGGAAAAAAAC[-/TAAT]TAGATTTTGTCCTCA | 51366 |
rs756980801 | snp | A/G/T | 3.30542e-05 | 0.00406524 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285596 | TATACTTAGGAATAA[A/G/T]GCCCATCAAGTCCGA | 51366 |
rs756990782 | in-del | -/A | 1.7513e-05 | 0.00295908 | intron-variant | UBR5 | GRCh38.p7 | 8:102265065 | AAATTGAAATGTTTT[-/A]AAAAAATTCAAACCC | 51366 |
rs756999257 | snp | A/C | 1.67882e-05 | 0.00289721 | intron-variant | UBR5 | GRCh38.p7 | 8:102299015 | AAACAACAATGAAGA[A/C]GACACAGTAAAAGAA | 51366 |
rs757020954 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102392532 | TAAGGAAAGCCTCCT[A/C]AAGAAAATACAGGAA | 51366 |
rs757033241 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102385124 | ACTGTTAAATGAGAC[A/G]CGTAAAAAGGAATTT | 51366 |
rs757038576 | snp | C/T | 1.65861e-05 | 0.00287972 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102312212 | TCCTTTGGAAACAGT[C/T]GGGAACCTTCGGTGT | 51366 |
rs757051728 | snp | C/T | 1.65938e-05 | 0.00288039 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295260 | CAAGGCATTCCAGTC[C/T]TGTAGAACACGCTCC | 51366 |
rs757070486 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102282705 | GGGTGGTGGCGACGG[A/G]AGGATCCAAATAAGA | 51366 |
rs757083842 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102332120 | CCCACCTGGTAATGG[A/G]AGACACGACAATCGA | 51366 |
rs757114476 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102393592 | AATGAGCTGAGATCA[C/T]GCCACTGCACCCCAG | 51366 |
rs757115830 | snp | A/G | 1.65839e-05 | 0.00287953 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102277189 | ACATTTTTGTTGGAA[A/G]AACCTATGAATATTT | 51366 |
rs757117634 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102256967 | CCGGGGCAATGTTCC[A/C]GGAGTACAGAAAGGA | 51366 |
rs757123167 | snp | G/T | 1.68539e-05 | 0.00290287 | intron-variant | UBR5 | GRCh38.p7 | 8:102299551 | CAATGTCACCATCTT[G/T]CAGTAAACAGAACAG | 51366 |
rs757130143 | snp | C/T | 1.64846e-05 | 0.0028709 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102278873 | TTAAACATTTCCCAC[C/T]ACTGGCAGATGAAGA | 51366 |
rs757132181 | snp | C/T | 1.64743e-05 | 0.00287 | intron-variant | UBR5 | GRCh38.p7 | 8:102268962 | ACTGAAATGCCTTCC[C/T]AATTGTACACATTAC | 51366 |
rs757168427 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102282908 | TACACACACTGCTAC[C/T]GAGACTGTCTTCCTT | 51366 |
rs757181293 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102350944 | AGCAAATGAAAAGAT[G/T]TTTAACACCATTAAT | 51366 |
rs757208760 | snp | A/G | 6.99215e-05 | 0.00591235 | intron-variant | UBR5 | GRCh38.p7 | 8:102361654 | ACATTAACAAACCAC[A/G]TGTACAGATCTTTTG | 51366 |
rs757210385 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102313484 | CTCAACTAGAACTAA[C/G]AGATCCAACAAATGG | 51366 |
rs757214594 | snp | C/T | 1.64773e-05 | 0.00287026 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102342555 | TCCAAGTTTGGCTCT[C/T]CTTCCTTGCTGGTAG | 51366 |
rs757223573 | snp | A/T | 1.70124e-05 | 0.00291649 | intron-variant | UBR5 | GRCh38.p7 | 8:102314738 | CATACAACAAATAAA[A/T]CTTACTGTATGGCAT | 51366 |
rs757227752 | snp | C/T | 0.000164726 | 0.0090739 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102289506 | CATCTCTGCCCCGAA[C/T]GGGCTGTGACTGGCT | 51366 |
rs757231858 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102381192 | TCAACATGGTGAAAC[C/T]CCGTTTCTATGAAAA | 51366 |
rs757234443 | in-del | -/AAC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102351106 | GGGATTGTAAAACGG[-/AAC]AACCACTTTCGGAAA | 51366 |
rs757240503 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102337664 | TATGTGTTGAATTCA[A/G]TTTCCTGAATTTTTT | 51366 |
rs757249799 | snp | C/T | 1.65143e-05 | 0.00287348 | intron-variant | UBR5 | GRCh38.p7 | 8:102295373 | AACAAAAATAAAACA[C/T]ATTGCTTCCCACAAG | 51366 |
rs757255142 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102405363 | AATAAAAGGCTTAAA[A/C]ATAATACTCAGGGGA | 51366 |
rs757267841 | snp | C/T | 0.000103332 | 0.00718718 | intron-variant | UBR5 | GRCh38.p7 | 8:102345363 | ACAGCTAGCCTGTGA[C/T]CAAAATAAATATATA | 51366 |
rs757268212 | in-del | -/CCT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102396332 | CAGACATTAAATACA[-/CCT]CCTCATCTTACAAAT | 51366 |
rs757322748 | snp | A/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311391 | CCATTCCAAGACTAC[A/T]AATAGGTGGAAGATC | 51366 |
rs757323437 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102393683 | GCCTGTAATCCCAGC[A/T]CTTTGAGAGGCTGAG | 51366 |
rs757328953 | snp | A/G | 5.52425e-05 | 0.0052553 | intron-variant | UBR5 | GRCh38.p7 | 8:102257767 | CCAGTTGTTGTTATT[A/G]TCTGTAGAATATTAC | 51366 |
rs757349252 | in-del | -/T | 1.73012e-05 | 0.00294114 | intron-variant | UBR5 | GRCh38.p7 | 8:102299959 | TTTCATGACCTGCTC[-/T]TTTTGTTAAACACTA | 51366 |
rs757357652 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102386164 | ACCAGGTGCAGTGAC[C/T]CACGCCTGTAATCCC | 51366 |
rs757376006 | snp | C/T | 1.66153e-05 | 0.00288225 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102275538 | CTAGTGACAAATCTC[C/T]TGACTGCTGGTTTCT | 51366 |
rs757400277 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102351550 | CTCTTGTTATTTAAC[A/G]GGTATAAAGTTCCAA | 51366 |
rs757403842 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102407656 | TAACTTGGGAGGCTG[A/C]GGAAGGAGAATCGCT | 51366 |
rs757414374 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102314856 | CTTACTTTCAGGCCT[C/G]AGATAAGAAATAAGA | 51366 |
rs757418785 | snp | C/G/T | 0.000115361 | 0.00759397 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102281450 | AGACCGCATTAGAGA[C/G/T]AGAGCATAATTTAGG | 51366 |
rs757446388 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102326776 | TTCTCCAGTATTTTC[A/G]CCTCAGAAAACTATT | 51366 |
rs757495532 | snp | C/T | 4.95823e-05 | 0.00497882 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102297563 | TGATGGGCAAACCAT[C/T]CCCATGAATACATCT | 51366 |
rs757503422 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102382579 | AATAATTTTTTTAAA[A/G]CCTGAAGATCAACAG | 51366 |
rs757524091 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102387924 | AGACCCTTAAAAACT[A/G]TCTAGTCTCACATCC | 51366 |
rs757548347 | in-del | -/TGTT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102371554 | GTACTTTGAGTACAC[-/TGTT]TGTCCATGCCTGATT | 51366 |
rs757563030 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102413070 | TGTGTTCTTTCGCTC[A/G]GATTCCCCTGGGGCA | 51366 |
rs757565004 | snp | C/G | 3.29669e-05 | 0.00405984 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102360178 | TGCCCCCGAGTTGCT[C/G]TTCAACTTTGACCTG | 51366 |
rs757612715 | snp | G/T | 6.62328e-05 | 0.00575431 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102293959 | GGATGCCTTACTTTT[G/T]CTTTTTGGATGAAGC | 51366 |
rs757614431 | snp | A/G | 3.29962e-05 | 0.00406165 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102275727 | CCAGGTTCTGCTCCA[A/G]CATCTTCCATGAATA | 51366 |
rs757622230 | snp | C/T | 1.6477e-05 | 0.00287024 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102329125 | CAGTTGCTCTTATGC[C/T]ATTTGCAGACAGGAG | 51366 |
rs757632264 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102327658 | TTTTAATTGAACTTC[C/T]CATGTTGGTATTCCA | 51366 |
rs757634805 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102364100 | AAAAGTCCACTAGGT[C/G]TCAAGTTCTCATCTA | 51366 |
rs757664667 | snp | C/T | 3.29544e-05 | 0.00405908 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102286448 | CATTGAACGGGGAGC[C/T]TGGGCAGCACCATTG | 51366 |
rs757667144 | snp | C/T | 3.30518e-05 | 0.00406507 | intron-variant | UBR5 | GRCh38.p7 | 8:102329237 | TTACTATTTTATATG[C/T]TGATATGTAGAGCTA | 51366 |
rs757673860 | snp | A/C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102277379 | ACCAACCTCAGATAA[A/C/T]TACTTTTTTTTTTTT | 51366 |
rs757735445 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102390780 | TACCATGTAGTCCAA[C/T]GCAAAATATCTGCAA | 51366 |
rs757735902 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102356963 | CTAAACTCAGTGAGC[A/G]AAAGTATGATGAGGA | 51366 |
rs757747024 | in-del | -/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102395887 | ACTCTTAATCCATTA[-/G]AAATCAAAGGTAAAC | 51366 |
rs757770176 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102388751 | AAGTCTCAGAATACA[C/T]CAAATATTTCACATT | 51366 |
rs757771885 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102377851 | GAGACAGCAATAGAT[A/T]TCAGTATTGTTTTTC | 51366 |
rs757778490 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102264877 | ACAATGCCCGCTAGT[A/G]TTTTTTTATTTTTAG | 51366 |
rs757799353 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102297903 | ACTCCTGGCTCTATT[C/T]AGCAAATTATAGACC | 51366 |
rs757799449 | snp | A/T | 1.6596e-05 | 0.00288058 | intron-variant | UBR5 | GRCh38.p7 | 8:102312322 | AATATTCACTTGCTG[A/T]ATAACTTCTTTACAC | 51366 |
rs757801270 | in-del | -/TT | | | intron-variant, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102258726 | GCTCACCATGAAAAA[-/TT]TTTGTTTGTATTCAT | 51366 |
rs757814282 | snp | A/T | 1.74193e-05 | 0.00295116 | intron-variant | UBR5 | GRCh38.p7 | 8:102261905 | TCAGAAAAGTGTATA[A/T]TTGCTTTACCTGTCC | 51366 |
rs757830480 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102308783 | GCATTGTAAATTGCA[C/T]ATTTTTTAAAAAGGC | 51366 |
rs757856383 | snp | A/G | 1.69286e-05 | 0.0029093 | intron-variant | UBR5 | GRCh38.p7 | 8:102300176 | CATGAACAAAATCAG[A/G]GCTCACTACCATATC | 51366 |
rs757856481 | snp | A/G | 1.6577e-05 | 0.00287893 | intron-variant | UBR5 | GRCh38.p7 | 8:102312489 | TACTTTTAGCACCTG[A/G]AAGTATAGGCAAATT | 51366 |
rs757858347 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102359104 | TTTTACTTTACCTAC[C/T]AATTTGTGGTCTGGA | 51366 |
rs757872409 | snp | A/G | 9.2262e-05 | 0.00679135 | intron-variant | UBR5 | GRCh38.p7 | 8:102275495 | CATACTACAGGTATA[A/G]TATAAGAAAATCTAA | 51366 |
rs757888487 | snp | C/T | 2.18138e-05 | 0.00330249 | intron-variant | UBR5 | GRCh38.p7 | 8:102312106 | ATGGAATATAGGATA[C/T]GCCAGCTGAAGAAGT | 51366 |
rs757910521 | snp | A/C/G | 4.94477e-05 | 0.0049721 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102327809 | GTAAAGAAACTATCC[A/C/G]CTCTCCTTGAAGTTC | 51366 |
rs757914830 | snp | C/T | 1.65116e-05 | 0.00287324 | intron-variant | UBR5 | GRCh38.p7 | 8:102360567 | TAAATACATATTAAA[C/T]AGAAAGGACATAATA | 51366 |
rs757927185 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102307640 | ATCTTCAGTTCCTCA[C/T]CTCTCATTTTCTCCT | 51366 |
rs757932109 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102386334 | ACCTGGGAGGCTGAG[G/T]CAGGAGAATCGTTTG | 51366 |
rs757939620 | in-del | -/AA | 1.79674e-05 | 0.00299722 | intron-variant | UBR5 | GRCh38.p7 | 8:102262107 | ACTCAGTTATGAAAG[-/AA]ACAGCATCTTCATTC | 51366 |
rs757969871 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102335851 | ACCGCGCCTGGCCCA[A/C]GTGCAGATATGCATG | 51366 |
rs757972853 | snp | G/T | 1.68858e-05 | 0.00290561 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102293735 | GAGCAATCCCCATTC[G/T]GACAGGAACAATCAG | 51366 |
rs757983990 | snp | A/G | 6.67022e-05 | 0.00577466 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102262047 | CATTACAGGATCAAA[A/G]AAAGCAAAATCATGC | 51366 |
rs757989367 | snp | C/T | 1.65274e-05 | 0.00287462 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285598 | TACTTAGGAATAAGG[C/T]CCATCAAGTCCGAGA | 51366 |
rs757991344 | snp | A/C | 1.66065e-05 | 0.00288149 | intron-variant | UBR5 | GRCh38.p7 | 8:102293938 | TATCTAAACCAAAAT[A/C]AAAAAGGATGCCTTA | 51366 |
rs758008421 | snp | A/T | 1.66183e-05 | 0.00288251 | intron-variant | UBR5 | GRCh38.p7 | 8:102312307 | CACGGAGTCAGTTCC[A/T]ATATTCACTTGCTGA | 51366 |
rs758021069 | snp | C/T | 1.6884e-05 | 0.00290547 | intron-variant | UBR5 | GRCh38.p7 | 8:102277219 | TACATTTAAAAGTTA[C/T]AAATGAAGGGAAAAA | 51366 |
rs758030109 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102260879 | CTAAAACAGTCATTT[G/T]GGTACCATAAGCACC | 51366 |
rs758057166 | snp | C/T | 1.75176e-05 | 0.00295947 | intron-variant | UBR5 | GRCh38.p7 | 8:102361665 | CCACGTGTACAGATC[C/T]TTTGTAAACAAATAC | 51366 |
rs758068418 | snp | A/G | 1.70749e-05 | 0.00292184 | intron-variant | UBR5 | GRCh38.p7 | 8:102299571 | AAACAGAACAGTAGG[A/G]TGTATATCATTATAG | 51366 |
rs758079071 | snp | A/C | 1.73975e-05 | 0.00294931 | intron-variant | UBR5 | GRCh38.p7 | 8:102285809 | AGGACAACCACAATG[A/C]GCTAATGTCAGTTGC | 51366 |
rs758080850 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102344407 | CAAGCTCTTCCTCCC[C/G]GGTTCATGCCATTCT | 51366 |
rs758104317 | snp | A/C | 6.59446e-05 | 0.00574177 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102278902 | GAATAAAGACCCTGA[A/C]TTGGACGGCCAAAAA | 51366 |
rs758111964 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102376944 | ATTAAAATATTCACA[A/G]AAGTAGGGGTCTGTT | 51366 |
rs758119564 | snp | C/T | 3.29913e-05 | 0.00406135 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102300074 | GGATCCTGGTGGTCA[C/T]TGGATGAAGCTCCAG | 51366 |
rs758128233 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102387548 | CCCGAAACCTCACCT[C/T]TACTAAAAACACAAA | 51366 |
rs758187137 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102336411 | CTTTTGAAGTTTGAG[-/T]TTTTGGTGTGAAATC | 51366 |
rs758192449 | snp | A/C | 3.31433e-05 | 0.0040707 | intron-variant | UBR5 | GRCh38.p7 | 8:102270027 | AGAGGTAACTAAGTA[A/C]ACAGTACACACTGGT | 51366 |
rs758230931 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102406087 | TTTTCTTCACAAGTG[G/T]CTGTTTATTCCTAGG | 51366 |
rs758245165 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102382691 | TTTTCAGGAGGAAAA[C/T]GTAGAGTTATTGCAA | 51366 |
rs758278656 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102333324 | TTTTTATTGTTTTTA[C/T]GAAGTACGAATTGCT | 51366 |
rs758295798 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102396709 | ACACATATATATATA[-/T]ATTTTTTTTTTTCTT | 51366 |
rs758298763 | snp | C/T | 3.314e-05 | 0.00407049 | intron-variant | UBR5 | GRCh38.p7 | 8:102270202 | TAAGAGAAGGAAAAC[C/T]ATTATGACTTCATTT | 51366 |
rs758301627 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102394806 | GCATTGGTTCCATTA[A/C]TCTAAGCCTAACCAA | 51366 |
rs758308707 | in-del | -/T | 3.74329e-05 | 0.00432609 | intron-variant | UBR5 | GRCh38.p7 | 8:102323541 | GACATAACTTTAAAA[-/T]ATATATATAATATTT | 51366 |
rs758317610 | snp | C/T | 1.65203e-05 | 0.002874 | intron-variant | UBR5 | GRCh38.p7 | 8:102288296 | TTATTTGTAGACAAT[C/T]AAAGCTAGTTAACTA | 51366 |
rs758330790 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102313532 | CGTATCTCTATGCAA[C/T]TTTTCTACAAAACTA | 51366 |
rs758364844 | snp | A/G | 3.3e-05 | 0.00406189 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102259074 | CTAAAATCTTCTGCC[A/G]TTAAATCTTCTAATG | 51366 |
rs758367438 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102304248 | GTCCACTAAACACTA[A/G]TCTCTATATATTTAG | 51366 |
rs758368303 | snp | A/G | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311399 | AGACTACTAATAGGT[A/G]GAAGATCCAGCCAAT | 51366 |
rs758375448 | snp | A/G | 1.68838e-05 | 0.00290544 | intron-variant | UBR5 | GRCh38.p7 | 8:102346185 | TAAATTCCACTCCCC[A/G]GTCGAAAGAGCACTC | 51366 |
rs758381375 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102256352 | GGAAATAGATTAAAA[C/T]AGATGACTTAGAACT | 51366 |
rs758390848 | snp | A/G | 1.6476e-05 | 0.00287014 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102289527 | GTGACTGGCTGATGC[A/G]CCTCTGCTGTGGATT | 51366 |
rs758439050 | snp | A/G | 1.64936e-05 | 0.00287168 | intron-variant | UBR5 | GRCh38.p7 | 8:102360193 | GTTCAACTTTGACCT[A/G]GGGGAAAGCAAGAGG | 51366 |
rs758445507 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102353972 | GGAGGCGGAGGCTGC[-/A]ATAAGCCAAAATCAT | 51366 |
rs758445655 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102326174 | CTCATGCTGACAACA[A/T]CCTCATAGAGCAGTA | 51366 |
rs758454498 | snp | C/T | 1.84875e-05 | 0.0030403 | intron-variant | UBR5 | GRCh38.p7 | 8:102298350 | ACAGAAGAGAATCTA[C/T]CCAAACTGAATGTAA | 51366 |
rs758467838 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102388217 | CCAATAAACTTTACA[G/T]GCAAACAGATGTGTC | 51366 |
rs758471168 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102340806 | TGCTATTTTAAATTT[A/G]GTATTTAATGGAAAA | 51366 |
rs758476700 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102299950 | ATTATTTCCTTTCAT[G/T]ACCTGCTCTTTTTGT | 51366 |
rs758477057 | snp | G/T | 1.65707e-05 | 0.00287838 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285146 | TGCCTTCAAGTGTTC[G/T]TAAGCTAGCTTCTTC | 51366 |
rs758503407 | snp | G/T | 1.64762e-05 | 0.00287016 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102329150 | CAGGAGGACTATCTT[G/T]TCATTGGTTAACCCC | 51366 |
rs758521229 | in-del | -/AA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102380383 | AACAAAGCTAGACTC[-/AA]AAAAAAAAAAAAAAC | 51366 |
rs758528804 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102339884 | ATGGATCAGAGGCAA[A/G]CCAATTCCAAGTTTA | 51366 |
rs758530071 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102401862 | CTTAAGGAAAACACC[C/T]AAGGATTTCCTGGAG | 51366 |
rs758543874 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102292071 | TTATTAAGAACATAA[C/G]AAGAACATTTTCAAG | 51366 |
rs758556351 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102339428 | CAGCTACTCAGGAGG[C/T]TGAGGCAGCAGAATT | 51366 |
rs758563713 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102328869 | CCTCCCAAAGTGCTC[A/G]GATTACGGGCGTGAG | 51366 |
rs758596582 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102310075 | CTATCACAACAAACC[A/G]CAACATGTTTAAAAC | 51366 |
rs758598515 | in-del | -/CAC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102370988 | TCCACTGTATATATA[-/CAC]CACATTTTTAACCAG | 51366 |
rs758618409 | snp | C/G | 3.30087e-05 | 0.00406242 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102275747 | TTCCATGAATACCCT[C/G]CCGAACAGTTCTAAA | 51366 |
rs758636830 | snp | C/G | 1.68809e-05 | 0.0029052 | intron-variant | UBR5 | GRCh38.p7 | 8:102275859 | GGGAAGGGGTGGGGG[C/G]GAGAAATAATTTAGC | 51366 |
rs758646033 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102305038 | GTTACATTTTCAAAA[C/T]TGCCTAAAACTCCCT | 51366 |
rs758655637 | snp | A/G | 1.65209e-05 | 0.00287405 | intron-variant | UBR5 | GRCh38.p7 | 8:102329264 | GCTATTCAATGCAAG[A/G]TTTCATAAAATAAAA | 51366 |
rs758657842 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102372840 | GATTAGAAATTCTTA[C/T]ATTGTACCACAAATA | 51366 |
rs758660908 | snp | C/G | 1.70295e-05 | 0.00291796 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102294103 | CTAGTGTACCTAGTA[C/G]AGTATCTAAAAGCTT | 51366 |
rs758674450 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102299123 | GCTCTGCAAGGAGCA[A/G]TTACAATTTTTTTTT | 51366 |
rs758677927 | snp | G/T | 1.70968e-05 | 0.00292371 | intron-variant | UBR5 | GRCh38.p7 | 8:102298817 | AAGCTAAGCTAAATC[G/T]TCACATGAAAAATAT | 51366 |
rs758690797 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102311080 | GATTTATATCTCTCC[C/G]CTTTGTGCTCCTACA | 51366 |
rs758701766 | snp | C/T | 4.96257e-05 | 0.004981 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295063 | TTGCTGATTGAGGTA[C/T]ACTTGCTCTTCTGGC | 51366 |
rs758716802 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102400668 | AACTAGACTGTGACC[C/T]TACAAGCACCGAAAT | 51366 |
rs758724862 | snp | A/C | 0.000101237 | 0.00711394 | splice-donor-variant | UBR5 | GRCh38.p7 | 8:102265098 | GATTAAAGTTCTTTT[A/C]CCTGCCAATGTTTCT | 51366 |
rs758727645 | snp | A/G | 1.64746e-05 | 0.00287002 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102313819 | CTTGCCAACAGGAAC[A/G]TTCTTGACATCTTCC | 51366 |
rs758773445 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102252971 | AAGAAAACAGTGTTA[C/T]TATGCCACTGAATAA | 51366 |
rs758780302 | snp | A/G | 1.66699e-05 | 0.00288698 | intron-variant | UBR5 | GRCh38.p7 | 8:102312509 | ATAGGCAAATTCAAT[A/G]AACATTAGCAATAGC | 51366 |
rs758783054 | in-del | -/A | 0.000101728 | 0.00713116 | intron-variant | UBR5 | GRCh38.p7 | 8:102326701 | GGTCAAATAAGCAGT[-/A]AAACAGCCCACTAAA | 51366 |
rs758792412 | in-del | -/GTATTTAGCTCTTAG | 1.66291e-05 | 0.00288345 | intron-variant | UBR5 | GRCh38.p7 | 8:102360708 | TCCAAGTAAAAATGT[-/GTATTTAGCTCTTAG]GTATTAAAATTTGAA | 51366 |
rs758810936 | in-del | -/AATT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102323100 | TAATAATAATAAATT[-/AATT]AATTAATTAATTAAT | 51366 |
rs758839781 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102264962 | GTGATCCTCCCAGTT[C/T]AGTCTCCCAAAGTGC | 51366 |
rs758841674 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102315287 | CATTAGACCATTAAT[A/T]TCATAGAGTTCCAAG | 51366 |
rs758852240 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102317242 | ACTCCCACCTGAATA[A/C]TGCGCTTTTCTGACG | 51366 |
rs758864526 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102334843 | GCAGAGCTTGCAAGG[A/G]GCCGAGATCGTGCCA | 51366 |
rs758878419 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102335829 | GCTAGGATTACAGGC[A/G]TGAGCCACCGCGCCT | 51366 |
rs758885576 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102367302 | TGCCAACTGTTTCAC[A/G]TTATCACTGATATCA | 51366 |
rs758886288 | snp | C/G/T | 4.99264e-05 | 0.00499607 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102361199 | CCAATACATTCAAAG[C/G/T]GGGGTGGCTGAGAGA | 51366 |
rs758890504 | snp | C/T | 0.00016494 | 0.00907981 | intron-variant | UBR5 | GRCh38.p7 | 8:102266897 | TTTATTGAAATTTCC[C/T]TGTAATTTAAATTCT | 51366 |
rs758892233 | snp | A/G | 1.74543e-05 | 0.00295412 | intron-variant | UBR5 | GRCh38.p7 | 8:102346876 | TTGTCCTGTTGTCTG[A/G]CATTAAGTGTTCTAC | 51366 |
rs758918338 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102252627 | AAATAGCATTTAGAC[A/G]TAAAAACCAATGTCT | 51366 |
rs758954103 | snp | C/T | 1.64917e-05 | 0.00287151 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102360652 | GAAAAACCAATCCTG[C/T]AAACTCTACCATCCT | 51366 |
rs758978476 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102279610 | AACTCACTGACAAAT[C/T]CAAACAGAGGAGATG | 51366 |
rs758989674 | snp | A/C | 2.07488e-05 | 0.00322087 | intron-variant | UBR5 | GRCh38.p7 | 8:102298502 | TCCCTAAAATAAGAA[A/C]AATTATATGTAAAAA | 51366 |
rs758995424 | snp | C/T | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102305115 | TTTCTTTATTGCTGG[C/T]TGGAAAGCAAACTGA | 51366 |
rs758995910 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102401516 | CTCAGCTCTCAAAAG[C/T]AGCAGAAAGATGAAC | 51366 |
rs759009740 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102348916 | TGGCTAAATAAAAAA[C/T]TGTTTAAATAGTTTC | 51366 |
rs759011106 | snp | A/T | 1.64825e-05 | 0.00287071 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102312447 | ACTGGAGGTTCCTGG[A/T]AATTTTACAGCAACA | 51366 |
rs759015401 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102358589 | CATATACTGTGTGCC[A/T]AGGACCATTAAAAGA | 51366 |
rs759036013 | snp | A/G/T | 3.35944e-05 | 0.00409833 | intron-variant | UBR5 | GRCh38.p7 | 8:102294974 | TAATACACATTCAAA[A/G/T]AACTTACCAAAATAT | 51366 |
rs759036640 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102279560 | AGATACCCACCACCC[A/G]AATACAGTTAGATTC | 51366 |
rs759062249 | snp | C/T | 1.64784e-05 | 0.00287035 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102286530 | TCCTGTTCTATGTCG[C/T]CACTCTGACTACTAC | 51366 |
rs759071919 | snp | C/T | 1.65594e-05 | 0.0028774 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102294072 | CCAGGTGTATATTTG[C/T]TTTGGAGTTCTTTCA | 51366 |
rs759077533 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102293143 | CCAGCAGAATTGGCA[A/T]CACCTGAGAACTTGA | 51366 |
rs759100029 | snp | A/G | 3.43236e-05 | 0.00414254 | intron-variant | UBR5 | GRCh38.p7 | 8:102265082 | AAAAATTCAAACCCA[A/G]GATTAAAGTTCTTTT | 51366 |
rs759101950 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102365192 | CTCACTGGCCAGGCA[C/G]AGTGGCTCATGCCTG | 51366 |
rs759103381 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102252393 | TAGGAAGACTTAAGA[C/T]ATTGTGCATTATTTT | 51366 |
rs759105633 | snp | A/G/T | 8.26199e-05 | 0.00642681 | intron-variant | UBR5 | GRCh38.p7 | 8:102329222 | AAGCATAAAAAAAAA[A/G/T]TACTATTTTATATGT | 51366 |
rs759111278 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102391397 | AAAAATGAATATACA[C/T]TGAGTATTGGATGAT | 51366 |
rs759131459 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102373766 | ATGCCATTAGATTCT[A/G]GAGAGTTTCTTTGTA | 51366 |
rs759156989 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102340858 | TTTGTTTCACATACC[A/G]CTCTTCTTCCATTCA | 51366 |
rs759158927 | snp | A/C | 1.66297e-05 | 0.0028835 | intron-variant | UBR5 | GRCh38.p7 | 8:102329406 | TGTTCCATCCTATAA[A/C]GTAAAATACAATACT | 51366 |
rs759182735 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102252340 | AAAAAAAAATCTTTT[A/C]CTATTATTAGAAGTA | 51366 |
rs759186337 | snp | A/G | 1.66568e-05 | 0.00288585 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102265263 | GACTAGAGCCATGGC[A/G]CTTTCGGTTTTCCTG | 51366 |
rs759205408 | snp | C/T | 1.65616e-05 | 0.00287759 | intron-variant | UBR5 | GRCh38.p7 | 8:102295162 | AGGTCTACACTAACG[C/T]AGGAAATACATAAAT | 51366 |
rs759210292 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102408391 | ATAGTATCTTACCTT[G/T]TGTTATGACACCTGA | 51366 |
rs759212451 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102399009 | ATATAAATGGCAAAC[A/T]GGTATATGATGAAAA | 51366 |
rs759222166 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102253460 | ATTTTCCAAAATGTA[C/T]CTTCAATAATCATGA | 51366 |
rs759230411 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102316835 | TATTATTACTGCCAC[A/G]AAACACCTGCAAAGG | 51366 |
rs759246514 | snp | A/G | 3.35824e-05 | 0.00409757 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102286601 | TTCAGAAAAGAAGGC[A/G]GGAACACTGCTTGCT | 51366 |
rs759254801 | snp | A/G | 1.64982e-05 | 0.00287208 | intron-variant | UBR5 | GRCh38.p7 | 8:102313789 | GTAATTAAGTTTTAG[A/G]TATCTTGAACAAACC | 51366 |
rs759289912 | snp | A/G | 1.64814e-05 | 0.00287061 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102346965 | GGGGCTGACTGCCCA[A/G]AAGCCCAGACCCTCG | 51366 |
rs759298747 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102380014 | AGTAACCATTAAAAT[A/G]ATGGAAATATAGTCT | 51366 |
rs759300325 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102400964 | TCATCAATCAATGTT[A/C]AGACAAAGAAAAGAG | 51366 |
rs759303021 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102298668 | GTGTACACTACATGA[C/T]GTTGAGACAGCCTCT | 51366 |
rs759303374 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102311615 | GAAACCTAGTATTCA[A/C]ATGTGCTAAATATTC | 51366 |
rs759306901 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102336470 | CAAGGAGCTTTCCTT[A/G]TATTTTCTCATAGTT | 51366 |
rs759333681 | in-del | -/TTC | 1.64787e-05 | 0.00287038 | cds-indel, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102342531 | CTTTGAACAGGTGTA[-/TTC]TTCTTATCCAAGTTT | 51366 |
rs759344284 | snp | A/G | 1.64955e-05 | 0.00287184 | intron-variant | UBR5 | GRCh38.p7 | 8:102287390 | GAATACACACACACA[A/G]CCTTAGCATAAGCAA | 51366 |
rs759357219 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102294197 | TTATAAGTTCTAACA[-/T]TTTTTTAAGTATTAA | 51366 |
rs759372671 | snp | C/T | 3.37308e-05 | 0.00410661 | intron-variant | UBR5 | GRCh38.p7 | 8:102280350 | GGGGAACTACTGAGG[C/T]AGCCATTTCTTGAAG | 51366 |
rs759382593 | in-del | -/ATA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102296856 | AAATCTAAACAGCTT[-/ATA]ATATTAAACTAAAGA | 51366 |
rs759388266 | snp | A/G | 1.65444e-05 | 0.00287609 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295659 | TGGCAGAGTAACCAG[A/G]TTAGTAGCAGTGAGC | 51366 |
rs759394728 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102335702 | TACAGGCATGTGCCA[C/T]CATGCCCAGCTAGTT | 51366 |
rs759418604 | snp | C/G | 1.71149e-05 | 0.00292526 | intron-variant | UBR5 | GRCh38.p7 | 8:102261305 | GCAATTTTGTCAAAG[C/G]AGTAAAACATTACTG | 51366 |
rs759420226 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102355692 | CACTGGCATCAAGTT[C/G]GTCAGGAGGCACTAT | 51366 |
rs759458351 | snp | A/G | 4.99588e-05 | 0.00499769 | intron-variant | UBR5 | GRCh38.p7 | 8:102272490 | GTTTGAGGAACAAGG[A/G]AAGAATTTTAAGCTG | 51366 |
rs759476843 | snp | G/T | 1.64874e-05 | 0.00287113 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102272665 | CTCATCCTTAAATGT[G/T]ACTTTTACTCTGTGT | 51366 |
rs759478915 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102354562 | TCACCTTACTATTTA[G/T]TAAACAAAAATAAAC | 51366 |
rs759488853 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102287338 | AATGCTTAGCTACCC[C/T]TGCGTATATCACACA | 51366 |
rs759509369 | in-del | -/AGGAAA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102373200 | AGCTCCGTTCGAAAC[-/AGGAAA]AGGAAAAGAATGCAC | 51366 |
rs759530470 | snp | C/G | 1.662e-05 | 0.00288266 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102347078 | CTTCCACCCACTCCA[C/G]AACTCCAGCGGCTTC | 51366 |
rs759570950 | snp | G/T | 1.66371e-05 | 0.00288414 | intron-variant | UBR5 | GRCh38.p7 | 8:102272790 | ATTAAAACACATCAA[G/T]AAGTCAAAAAGTAGT | 51366 |
rs759588590 | snp | A/G | 1.65671e-05 | 0.00287807 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102293679 | ACTGCCCTGCATGGC[A/G]TCTATGCTAGTACTA | 51366 |
rs759592991 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102261561 | CAAAAATTAGGTGGG[C/T]GTGGTGGCGCGTACC | 51366 |
rs759631066 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102331721 | CTTCTCTTTAAACTC[C/T]TCAAATGATTTGCCT | 51366 |
rs759657342 | snp | C/T | 1.65452e-05 | 0.00287616 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102327754 | CACCACCAATATAAA[C/T]TGTTTTCCAGCTGAG | 51366 |
rs759675726 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102307140 | GTATACTAAATGGCA[C/T]CACTAGCACTTGGAG | 51366 |
rs759678954 | in-del | -/TC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102261816 | GTACACACACGTTCA[-/TC]TCTTTCATTCCCTAA | 51366 |
rs759690709 | snp | C/T | 1.90246e-05 | 0.00308414 | missense, intron-variant | UBR5 | GRCh38.p7 | 8:102361585 | TAAAACTCTTACCTG[C/T]TTAAATTATATTTGT | 51366 |
rs759695045 | snp | C/T | 1.66183e-05 | 0.00288251 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285707 | AAGCAGCTGCTGCAG[C/T]TGCAGCACTTGTACT | 51366 |
rs759699466 | in-del | -/AAAA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102371277 | TATCCTTTTTTTTTA[-/AAAA]AAAAAAAAAAAAAAA | 51366 |
rs759704435 | snp | C/T | 1.64999e-05 | 0.00287222 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102261977 | CCATTGCTGAGAAAA[C/T]AGCATCAGCATCTGA | 51366 |
rs759704991 | snp | C/T | 1.6582e-05 | 0.00287936 | intron-variant | UBR5 | GRCh38.p7 | 8:102278798 | CCTTAATAAATGTTA[C/T]ATTGCAAAAAAACTT | 51366 |
rs759720493 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102342203 | TGCTGATGTGTTATC[C/T]AGAACTAACATCCTA | 51366 |
rs759728209 | snp | A/G | 1.67077e-05 | 0.00289026 | intron-variant | UBR5 | GRCh38.p7 | 8:102285493 | ATAGTGGAATGGGAA[A/G]CTTTTCAGTGGTTTC | 51366 |
rs759739729 | snp | A/T | 1.67413e-05 | 0.00289316 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102312169 | GCTAATATTTCTGTT[A/T]TTTCAGGTATACAAA | 51366 |
rs759741568 | snp | A/G | 4.96619e-05 | 0.00498282 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102298953 | TTGGATTCTACTACA[A/G]ATGGCTCTGTGGAAG | 51366 |
rs759742618 | snp | G/T | 1.64914e-05 | 0.00287149 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102277159 | TCATTACATTTTTCA[G/T]ATTGGCAGCATAAGA | 51366 |
rs759745669 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102355619 | CCAAGAGAAACAATC[A/G]GAATTTAACTGCTTA | 51366 |
rs759765253 | snp | A/G | 1.6557e-05 | 0.00287719 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102361187 | TAGTAGCCTGTTCCA[A/G]TACATTCAAAGGGGG | 51366 |
rs759774937 | in-del | -/AATT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102257228 | GTACCCACATATCAC[-/AATT]AAGCTACTCTCTTCC | 51366 |
rs759780884 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102375222 | AAAAATTAGTCAGGG[A/G]TGGTGGTGCACACCA | 51366 |
rs759820907 | snp | A/G | 4.94572e-05 | 0.00497254 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102288156 | AATAACCTGCATACC[A/G]TCTTCATCATGCTCA | 51366 |
rs759833723 | snp | C/T | | | intron-variant, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102258913 | ACAGGCCTTAAGAAC[C/T]AGAAACTCAGAAAAT | 51366 |
rs759837558 | in-del | -/AA | 0.00427195 | 0.0460188 | intron-variant | UBR5 | GRCh38.p7 | 8:102275623 | TTCAGTTAGGATCTT[-/AA]AAAAAAAAAAATGCA | 51366 |
rs759865943 | snp | A/G | 1.65304e-05 | 0.00287488 | intron-variant | UBR5 | GRCh38.p7 | 8:102267059 | AGACTTCTAGAATTT[A/G]GCGTATAATTTAAAT | 51366 |
rs759877167 | in-del | -/ATT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102347155 | GATTGCTTGGTTTTC[-/ATT]ATTATTATTTTCAGC | 51366 |
rs759881417 | in-del | -/GCAGCTGCT | 1.65996e-05 | 0.00288089 | cds-indel, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285694 | TTGCTAGCTTCCAAA[-/GCAGCTGCT]GCAGCTGCAGCACTT | 51366 |
rs759883179 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102302092 | AATTCAATATTAAAT[A/G]AGGGGGCCATTCCTT | 51366 |
rs759889289 | snp | A/T | 1.64852e-05 | 0.00287094 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102342628 | GTTCACGTAAACGTA[A/T]AACGGATTCACGTTC | 51366 |
rs759901170 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102352425 | ATTTTTAAAAACATT[C/T]AAGAGCTAAATATGT | 51366 |
rs759925235 | snp | A/C | 1.67335e-05 | 0.00289248 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102300007 | GCTCTTACCAGGATC[A/C]ATCGCAGGAGGGTCA | 51366 |
rs759951064 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102332838 | AGGCCAATATCATAC[G/T]CATGACTATATTACC | 51366 |
rs760014628 | snp | C/T | 6.59391e-05 | 0.00574153 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295434 | GGACTGGCTGTTTTT[C/T]GGTTACGATCTTCCC | 51366 |
rs760022842 | in-del | -/GGGGGG | | | intron-variant | UBR5 | GRCh38.p7 | 8:102283342 | TAGGAAGGGGAAGGC[-/GGGGGG]GGGGGGGGGTGAGTA | 51366 |
rs760036853 | snp | C/T | 1.64757e-05 | 0.00287012 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102288234 | TTCATCATGATGATC[C/T]TCTTCTCCAGCCACA | 51366 |
rs760056976 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102325437 | TAATAAAAAACTACC[A/C]TTTTGTCTAAGTTTT | 51366 |
rs760058027 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102404710 | GTCGGGAGTTCGAGA[C/T]CAGCCTGACCAACAT | 51366 |
rs760059144 | snp | C/T | 1.65416e-05 | 0.00287586 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102323355 | CATGTTTTTCAAGCT[C/T]TCAGGAGATCTAAGT | 51366 |
rs760071947 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102337860 | TCAGCAACATATTAT[C/G]AAATTTCTAATCTAG | 51366 |
rs760079392 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303517 | TAAATTTTTTTCCTA[A/C]AGAAAGAAAACTATA | 51366 |
rs760082662 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102252441 | TAACTATTAAAAATA[A/C]ATTCACAATTAGGGT | 51366 |
rs760089982 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102255598 | ATGACCTCACTGCTG[A/G]ATCTCTAAGAAGTTG | 51366 |
rs760103245 | snp | A/G | 1.64803e-05 | 0.00287052 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102342513 | TCTCCTAGAGATACT[A/G]GACTTTGAACAGGTG | 51366 |
rs760115624 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102311954 | AATAAACATCTACAA[A/T]ATTTTAACTTCTCTG | 51366 |
rs760121047 | snp | G/T | 2.16354e-05 | 0.00328896 | intron-variant | UBR5 | GRCh38.p7 | 8:102257748 | GTAAATAAAATATAC[G/T]ATACCAGTTGTTGTT | 51366 |
rs760123191 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102393425 | GCGGATCACGAGGTC[A/G]AGAGTTCGAGACCAG | 51366 |
rs760125551 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102269595 | CAAAAAACATAACTA[A/G]TTTGTGTTTCATATC | 51366 |
rs760128414 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102252655 | TCTCACTTTGTAAAA[C/T]AACCTTTGGCTAATT | 51366 |
rs760130547 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102281987 | TATCCTGGGCAACAT[A/G]GTGAAACCCTGTCTC | 51366 |
rs760144165 | snp | A/G | 1.64887e-05 | 0.00287125 | intron-variant | UBR5 | GRCh38.p7 | 8:102267037 | CCTTTCACATTCCAG[A/G]TAACGGAGACTTCTA | 51366 |
rs760147989 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102385707 | CAGGAACAAGCTACT[C/G]CACCCAGCTAATCCC | 51366 |
rs760158433 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102348497 | TAGAAAGGGCATGAC[A/G]TCTACATCTTCTCTT | 51366 |
rs760158916 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102267390 | TGATTCTAGAACACC[A/G]ATAAATTCACTGTTT | 51366 |
rs760170654 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102345877 | ACCATCCTGGCTAAC[A/G]TGGTGAAACCCCGTC | 51366 |
rs760185438 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102353580 | GGGATCTTAGAACAG[-/A]AAAAGGGCATTATGA | 51366 |
rs760188972 | snp | A/C/T | 3.36096e-05 | 0.00409926 | intron-variant | UBR5 | GRCh38.p7 | 8:102280515 | AGTATTTGTATAATA[A/C/T]GAACAGGAGCAAAAG | 51366 |
rs760196546 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102350150 | CCATGTTTGTGCCAC[C/T]GCACTCCAGCCTGGG | 51366 |
rs760216383 | snp | C/T | 5.33433e-05 | 0.00516418 | utr-variant-3-prime, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102254300 | TACACACTTTTTATA[C/T]TCTACACAAAACCAA | 51366 |
rs760228803 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102312820 | CGGTCTGACAGAACT[C/T]TCTTGAAAATGGCAA | 51366 |
rs760229040 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102399142 | TTACTCAAGGTCATA[C/T]CATCATATGGCCAGT | 51366 |
rs760256110 | snp | A/G | | | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102300037 | AGGAACCCAACTAGG[A/G]GGAGCTATGGGGGGT | 51366 |
rs760262126 | snp | A/T | 1.64811e-05 | 0.00287059 | intron-variant | UBR5 | GRCh38.p7 | 8:102313801 | TAGATATCTTGAACA[A/T]ACCTTGCCAACAGGA | 51366 |
rs760280538 | in-del | -/A | 1.6684e-05 | 0.00288821 | intron-variant | UBR5 | GRCh38.p7 | 8:102311718 | TCACTTTTCAAAAGC[-/A]AAAAATGAGCCTCTA | 51366 |
rs760308015 | snp | A/G | 1.81684e-05 | 0.00301395 | intron-variant | UBR5 | GRCh38.p7 | 8:102254523 | AGTAAACCTGAACAG[A/G]AATTTAACAGGTTAA | 51366 |
rs760311537 | snp | A/C | 1.66056e-05 | 0.00288141 | intron-variant | UBR5 | GRCh38.p7 | 8:102305061 | AACTCCCTTTAAAGA[A/C]CTTGCTATAGTTCTT | 51366 |
rs760314497 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102380191 | TTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGACC | 51366 |
rs760315651 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102362109 | AACGGTCTTATAGCA[C/G]AAAATTGAACAAACC | 51366 |
rs760322689 | snp | C/T | 3.29565e-05 | 0.00405921 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102346978 | CAAAAGCCCAGACCC[C/T]CGATCCCGTCCTGTC | 51366 |
rs760326805 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102392436 | AAATGTTTACAATAG[A/T]ATACTGGAAAAAACA | 51366 |
rs760330526 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102379431 | AGTCTTATTAGAATA[C/T]TATCAATAAATAATA | 51366 |
rs760334449 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102397449 | CGTAATCCCAGTACT[C/T]TGGGAGGCCAAGGCA | 51366 |
rs760370253 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102368126 | TTGACAACACACACA[C/G]AAAAAAAAATCACTA | 51366 |
rs760377438 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102273816 | TAAAATGTATAGTAT[A/G]TTTGGGGAGGTGGGA | 51366 |
rs760384963 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102321220 | AAATCACCTTAAGCT[A/G]ATAAGCAACTTCAGC | 51366 |
rs760436256 | snp | C/T | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102305204 | AGCATCTGTAGATTC[C/T]GCTCTAAAACAACCG | 51366 |
rs760436367 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102369339 | AGCAATGTGGAAATC[A/T]GAAACCTATTAATGA | 51366 |
rs760440241 | in-del | -/AT | 2.81053e-05 | 0.00374858 | intron-variant | UBR5 | GRCh38.p7 | 8:102298516 | AAATTATATGTAAAA[-/AT]ATATTAATTACTACT | 51366 |
rs760442438 | in-del | -/AAAG | | | intron-variant | UBR5 | GRCh38.p7 | 8:102284254 | AGGGGAGGCAGAAAA[-/AAAG]AAATGTGATTTGAGA | 51366 |
rs760443756 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102253746 | CTAGAGCTCAATGCA[C/G]TCAAACCGCAATAAA | 51366 |
rs760447343 | snp | C/T | 1.73815e-05 | 0.00294795 | intron-variant | UBR5 | GRCh38.p7 | 8:102347133 | TAGCATTTTAAACAA[C/T]CATTCTGATTGCTTG | 51366 |
rs760450186 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102301452 | GTTAATTATTTTATA[A/G]TATCAATGTCTTCTT | 51366 |
rs760453043 | snp | A/C/T | 4.92432e-05 | 0.00496182 | intron-variant | UBR5 | GRCh38.p7 | 8:102297034 | ATAAGTATGCATATA[A/C/T]CTCATCATAATAATT | 51366 |
rs760469908 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102324832 | AATGTTAAGACATGA[A/G]TATTTTACTTGTTCT | 51366 |
rs760481562 | snp | C/T | 1.66532e-05 | 0.00288554 | intron-variant | UBR5 | GRCh38.p7 | 8:102293863 | GAACAAAAAGAGAAA[C/T]ATCAGCAATCTATCT | 51366 |
rs760509388 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102294318 | TGAGTCCTAAATGTA[C/T]GATTTCTTATTTTTT | 51366 |
rs760523471 | snp | C/T | 1.6777e-05 | 0.00289624 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102293714 | GGGTAAATGGTGCAG[C/T]TGGACGAGCAATCCC | 51366 |
rs760534593 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102261752 | CCTCAGTCTGTCTCA[C/G]TAACTCTTGATCCAT | 51366 |
rs760556988 | snp | C/G | 1.65963e-05 | 0.0028806 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102312196 | CAAAGCTTTTTAGGA[C/G]TCCTTTGGAAACAGT | 51366 |
rs760559966 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102272461 | ACATATAGAAACCAT[A/G]ATTACCACTGTTGGT | 51366 |
rs760597254 | snp | A/G | 1.66493e-05 | 0.0028852 | intron-variant | UBR5 | GRCh38.p7 | 8:102272793 | AAAACACATCAAGAA[A/G]TCAAAAAGTAGTAAA | 51366 |
rs760600987 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102356569 | TCGAGACCGTCCTGG[A/C]CAACATGGCAAAACC | 51366 |
rs760608173 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102308132 | AAATTTCACCTGTCT[A/G]AAACCAAATTCCTGA | 51366 |
rs760613361 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102263002 | GACACAGGAGAATCA[C/G]TTGAACCTGGGAGAT | 51366 |
rs760633075 | snp | A/G | 1.90882e-05 | 0.00308929 | intron-variant | UBR5 | GRCh38.p7 | 8:102327916 | AGAATAAAATATTAG[A/G]ACTTTAAATAAAATC | 51366 |
rs760661546 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102283348 | GGGGAAGGCGGGGGG[G/T]GGGGGGGGTGAGTAG | 51366 |
rs760687431 | snp | C/T | 3.29962e-05 | 0.00406165 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102262004 | CTGAACTCTGAGACG[C/T]GAGGATTAGTTGCCG | 51366 |
rs760697424 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102370457 | AACTGATAGATATAT[C/T]TATGGGGTGCATGCA | 51366 |
rs760702350 | snp | C/G | 1.85679e-05 | 0.0030469 | intron-variant | UBR5 | GRCh38.p7 | 8:102262116 | TGAAAGAAACAGCAT[C/G]TTCATTCAATTAATT | 51366 |
rs760707183 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102388272 | AGCTACACATTTATT[G/T]CAACAATAATGCCCC | 51366 |
rs760714437 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102393354 | TGAATGTAAAAACGG[A/G]AACAACAGGCGGTGG | 51366 |
rs760716478 | snp | C/T | 6.67936e-05 | 0.00577861 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285739 | ATGGTACCACTCCGG[C/T]GTAAGTTTGAAGGAT | 51366 |
rs760729266 | in-del | -/ATGGTGCCTTCAA | 0.000115816 | 0.00760886 | intron-variant | UBR5 | GRCh38.p7 | 8:102360043 | CAGACCATCTGTAAG[-/ATGGTGCCTTCAA]CTGGCCACAACTTAC | 51366 |
rs760744999 | snp | A/T | 4.99355e-05 | 0.00499652 | intron-variant | UBR5 | GRCh38.p7 | 8:102312286 | TTTCAAACTCCATAA[A/T]AAACTCACGGAGTCA | 51366 |
rs760804588 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102282830 | GGTCACACCCACTGG[G/T]ATGGTTATAACAAAA | 51366 |
rs760805061 | snp | G/T | 1.64955e-05 | 0.00287184 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102278835 | TCTTACCTCTAGGCA[G/T]TTTCTATCCACTGTA | 51366 |
rs760816003 | snp | A/T | 1.75962e-05 | 0.00296611 | synonymous-codon, intron-variant | UBR5 | GRCh38.p7 | 8:102361614 | GTTCAGCTTCTCAGA[A/T]ACTTCTCGTAACCTT | 51366 |
rs760817843 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102405916 | CTTTAATATACCTTA[C/T]AAGATCTACGTCCAT | 51366 |
rs760819534 | snp | C/T | 6.80561e-05 | 0.00583296 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102345522 | CAGAATGAATGTCGG[C/T]ATCAAGGAGAGACAT | 51366 |
rs760823538 | snp | C/T | 1.65274e-05 | 0.00287462 | intron-variant | UBR5 | GRCh38.p7 | 8:102279033 | CTAACTTGTTTAATT[C/T]ACCTGCAACAGATGT | 51366 |
rs760825996 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102377431 | GTACAATACTGGCCA[G/T]GCGTGGTGGCTCACG | 51366 |
rs760830863 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102296390 | TCCTAAAACACCACA[A/G]ATGTTAGTGCTAGGT | 51366 |
rs760838067 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102376685 | ATTTTTTTGTATTTT[C/T]AGTAGAGACAGGGTT | 51366 |
rs760847140 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102376751 | CCTCGTGATCTGCCC[A/G]CCTAGGCTTCCCAAA | 51366 |
rs760886424 | snp | A/C | 1.66449e-05 | 0.00288482 | intron-variant | UBR5 | GRCh38.p7 | 8:102269995 | ATTCAAAAGCAAAAA[A/C]ATAACACAGCCAGTT | 51366 |
rs760889124 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102353119 | CTCTAACCAGCTCAC[C/T]ATCTATATAAAGATT | 51366 |
rs760900237 | snp | C/T | 8.55688e-05 | 0.00654042 | intron-variant | UBR5 | GRCh38.p7 | 8:102345387 | ATATATAAATAAATG[C/T]AAAATTACCTCGAGA | 51366 |
rs760907935 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102331914 | TTCTCCCTGTATTCA[A/T]ATTGTGCTTCACCTT | 51366 |
rs760912771 | snp | C/T | 1.65053e-05 | 0.0028727 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102342653 | ACGTTCACGCAACAG[C/T]TCAGAGTCTCTCTCT | 51366 |
rs760938874 | snp | A/T | 4.9527e-05 | 0.00497605 | missense, nc-transcript-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102412178 | GCCCTATTACCTGTC[A/T]TTGAGCTGGTCCTCG | 51366 |
rs760940800 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102269732 | CCAAAAGTAGTAATA[A/G]TTTGTTCAAATGAAG | 51366 |
rs760946699 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102407428 | CATGAGCCACTGGCC[A/G]GGCCTTAATCTTAAT | 51366 |
rs760962785 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303782 | CTAACTTCCTAGGAA[A/G]CAAGAATGATGAATT | 51366 |
rs760968359 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102325738 | AAATATTTAATAGTG[A/G]TAAAACCCCACATTC | 51366 |
rs760971442 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102393559 | GAGAATCGCTTGAAC[C/G]TGGGAGGTGGAGGTT | 51366 |
rs760971862 | snp | C/G | 2.28016e-05 | 0.00337643 | intron-variant | UBR5 | GRCh38.p7 | 8:102257753 | TAAAATATACTATAC[C/G]AGTTGTTGTTATTAT | 51366 |
rs760983669 | snp | C/T | 1.6507e-05 | 0.00287284 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102259038 | TGCACATTGACTTCA[C/T]CGCAGCCATTTACCA | 51366 |
rs760992357 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102268684 | TGGCAAGAACACAGT[A/G]TAATATGTATGGCCT | 51366 |
rs761010302 | snp | A/C | 1.67764e-05 | 0.00289619 | intron-variant | UBR5 | GRCh38.p7 | 8:102281534 | TCTATAAGAACAGAA[A/C]GGAAAATGTTTATTA | 51366 |
rs761041677 | in-del | -/TACCTT | 1.72487e-05 | 0.00293667 | intron-variant | UBR5 | GRCh38.p7 | 8:102275512 | ATAAGAAAATCTAAA[-/TACCTT]TACCTCTAGTGACAA | 51366 |
rs761081006 | snp | C/G | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311478 | TACCATTTCCATCTC[C/G]AAGAATAATGGGAGA | 51366 |
rs761084801 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102352542 | GATAGTGCCAGTTTA[A/G]GCCTATTGGCTAAGC | 51366 |
rs761161384 | snp | C/T | 3.32923e-05 | 0.00407983 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102314798 | CACTACACGTGGATG[C/T]TGGAGATGGTGGAGG | 51366 |
rs761188913 | snp | C/T | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102289500 | GTTCTTCATCTCTGC[C/T]CCGAACGGGCTGTGA | 51366 |
rs761205539 | snp | A/G | 1.67483e-05 | 0.00289377 | intron-variant | UBR5 | GRCh38.p7 | 8:102311695 | CACAAAAATGCCATT[A/G]TTGTCCTATCACTTT | 51366 |
rs761219166 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102327502 | TTGCAGGATTCTAAA[C/T]GACTTTTGTTTCTAC | 51366 |
rs761229079 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102288714 | AAAATAAAAAAATTA[C/T]ACCCACAGATCCCAA | 51366 |
rs761230413 | snp | G/T | 1.69341e-05 | 0.00290977 | intron-variant | UBR5 | GRCh38.p7 | 8:102259167 | ATACTTCATTTTCCA[G/T]GTAACATTTATTTAT | 51366 |
rs761232034 | in-del | -/AC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102392480 | ACTAAAGCTACACAA[-/AC]ACACACACACACACC | 51366 |
rs761247633 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102301815 | TCACAAACTCAATGG[C/G]TAATGGGTCAGAAAG | 51366 |
rs761253457 | in-del | -/TGAG | 6.63119e-05 | 0.00575774 | intron-variant | UBR5 | GRCh38.p7 | 8:102288127 | CTGATTTACTCATAC[-/TGAG]TAATTTCTCAAATAA | 51366 |
rs761256334 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102384134 | GAAAACGACACAGAA[C/T]TTTCTAAACAATCAA | 51366 |
rs761266396 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102363647 | AACTAAACTCATTCA[C/T]TTCCATTCCTTTGTT | 51366 |
rs761272087 | snp | A/G | 2.04648e-05 | 0.00319874 | intron-variant | UBR5 | GRCh38.p7 | 8:102257739 | ATGAAGAATGTAAAT[A/G]AAATATACTATACCA | 51366 |
rs761274479 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102383370 | TCAGCCAGAGTACTA[A/G]TAGCCTGGGAATACA | 51366 |
rs761282456 | snp | A/G | 1.64963e-05 | 0.00287192 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311321 | GCCATGATGATAACA[A/G]CAGCTTTCTTTTTGA | 51366 |
rs761285309 | snp | C/T | 1.66004e-05 | 0.00288096 | intron-variant | UBR5 | GRCh38.p7 | 8:102288120 | AAAGTACCTGATTTA[C/T]TCATACTGAGTAATT | 51366 |
rs761290232 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102325223 | ATATAAATAATGAAG[A/G]CCGATCAATAATGTT | 51366 |
rs761320649 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102321530 | AAGGTAATTTATAGA[C/T]TCAATGGTATCCCCA | 51366 |
rs761326850 | in-del | -/AAAGGA | 3.87289e-05 | 0.00440034 | intron-variant | UBR5 | GRCh38.p7 | 8:102297007 | TAAGAGTGTACTTTT[-/AAAGGA]ATAATTATAAGTATG | 51366 |
rs761327439 | snp | A/G | 1.65589e-05 | 0.00287736 | intron-variant | UBR5 | GRCh38.p7 | 8:102360030 | CAGGAAGATGATACA[A/G]ACCATCTGTAAGATG | 51366 |
rs761332021 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102259218 | AATTTTAGCAGCCTT[A/C]TCTAACAATGCTAGT | 51366 |
rs761352689 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102380535 | TAAGGGGAAAAAAGT[C/G]AGGTATCAGTAGCGA | 51366 |
rs761373189 | snp | C/T | 1.64757e-05 | 0.00287012 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102281372 | TGCTTGAAAAACATA[C/T]GCCACATGCTTCAAT | 51366 |
rs761385720 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303277 | ACCCATGAATACTTT[C/T]TGATAAATCTCACTT | 51366 |
rs761393805 | snp | C/T | 0.000214707 | 0.0103589 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102281492 | TGCAGACATCATTCC[C/T]TGACGGGCGCTAAGC | 51366 |
rs761394714 | snp | C/G | 1.65026e-05 | 0.00287246 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102262013 | GAGACGCGAGGATTA[C/G]TTGCCGCAAACTCTC | 51366 |
rs761404993 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102360321 | GATTTGACTTGGTAC[C/T]TACTAAACACGTAAT | 51366 |
rs761415814 | in-del | -/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102277687 | AACCAGCCTTACCCA[-/C]CCCCCTCCTTTAAAT | 51366 |
rs761472650 | snp | A/G | 1.64808e-05 | 0.00287057 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102327788 | AGGTGTAAAGGGCAC[A/G]GCAATGTAAAGAAAC | 51366 |
rs761477693 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102382000 | ACAGATATTTCCATT[C/T]AATAGTGAGTCTTTG | 51366 |
rs761505270 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102309472 | TGTACAGTAATAACA[C/T]AAGCCCTCACATTCA | 51366 |
rs761527275 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102327307 | CACAACAAAGAAAAA[A/C]TGTAAGGTCACCTTC | 51366 |
rs761527917 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102398674 | TAATCCCAGGTACTC[A/G]GGAGGCTAAGGCAGG | 51366 |
rs761543484 | snp | C/T | 1.64806e-05 | 0.00287054 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102360141 | GAGAGTCGCTTGTCC[C/T]ACCAGGCCTTGACGT | 51366 |
rs761574860 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102273918 | ATGGTAAAAGAGACA[A/G]GAATGGACTTATATC | 51366 |
rs761587784 | snp | A/G | 1.65756e-05 | 0.00287881 | intron-variant | UBR5 | GRCh38.p7 | 8:102329045 | AGAAAAAAAGAAAAC[A/G]AGAATTAAAGCATGA | 51366 |
rs761588027 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102296473 | GTTGCTGAATGAAAG[A/T]CTGTTGCATTTAGTT | 51366 |
rs761600921 | snp | A/C | 5.00029e-05 | 0.0049999 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102286370 | CTTGCCTGCTGGTGT[A/C]GATGTACTGGAAGGG | 51366 |
rs761606096 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102308340 | CCTCTTGCTTCGTCT[A/G]TTTGATACCCTACAT | 51366 |
rs761649617 | snp | C/T | 1.66743e-05 | 0.00288736 | intron-variant | UBR5 | GRCh38.p7 | 8:102293894 | TTTCATATACATAAA[C/T]CACTATCACAAAAAC | 51366 |
rs761650789 | in-del | -/AAG | | | intron-variant | UBR5 | GRCh38.p7 | 8:102272788 | CTATTAAAACACATC[-/AAG]AAGTCAAAAAGTAGT | 51366 |
rs761652510 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102399630 | AGTTTTCTTTAAACT[A/G]TGTCTTCAAATCTAT | 51366 |
rs761686710 | snp | G/T | 1.65203e-05 | 0.002874 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102300046 | ACTAGGGGGAGCTAT[G/T]GGGGGTGAAACTGGA | 51366 |
rs761689021 | snp | C/T | 3.29848e-05 | 0.00406095 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102279093 | CAGAGGCACTTCAAA[C/T]GGATTTGGGGGTATA | 51366 |
rs761715258 | snp | A/G | 7.44907e-05 | 0.00610244 | intron-variant | UBR5 | GRCh38.p7 | 8:102264438 | AAGAAAATTTTTGCA[A/G]TTGTGAATACAATTA | 51366 |
rs761736516 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102274880 | TGCATTCCCAAACTG[C/T]TATCAATTAAAAAGG | 51366 |
rs761737763 | snp | C/T | 3.38181e-05 | 0.00411192 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285771 | AATATAAATCAAACC[C/T]GCTGAACTTGCTATA | 51366 |
rs761740218 | snp | A/G | 1.6489e-05 | 0.00287128 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295475 | TGGCCTGTATTGACA[A/G]TGCTCCACCGTCTGC | 51366 |
rs761753795 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102395118 | AGCTCTCCCACCAGC[A/C]TCTCTCAGCCTACCT | 51366 |
rs761763970 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102346740 | AGCCTGGGCAGCAGA[G/T]TGAGACTCCCTCTCA | 51366 |
rs761767500 | snp | A/G | 1.6486e-05 | 0.00287102 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102312403 | GAAGGGTCAGCATCT[A/G]GACCAGAGCTGTTCT | 51366 |
rs761771026 | snp | C/T | 1.65173e-05 | 0.00287374 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102294040 | TCATTGTCACAGCAA[C/T]AGCTTCTTCTCTACG | 51366 |
rs761789536 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102333250 | AATACAAAACAATCA[A/T]ATACATACACAAGGA | 51366 |
rs761804737 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102377565 | ACAAAAATTAGCCGG[A/G]CATTGTTGGACGCGC | 51366 |
rs761842866 | snp | A/C/T | 3.59215e-05 | 0.00423786 | intron-variant | UBR5 | GRCh38.p7 | 8:102264444 | ATTTTTGCAATTGTG[A/C/T]ATACAATTAGGTTCA | 51366 |
rs761899496 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102259394 | GATTTAACAATTTTA[A/C]AAGTTTTGTTAATAA | 51366 |
rs761925037 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102284683 | TAAACTCATCATAAA[C/T]GCATAAAGTCTAAAC | 51366 |
rs761931567 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102254093 | TAGACCCAGAAGTTG[G/T]TGACTAGCAAACCAA | 51366 |
rs761941996 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102269870 | CAGTTACCCTTCAGT[A/G]AACACTGCCTTATTC | 51366 |
rs761952460 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102270756 | ACTCCTGAACTCAGA[G/T]GATCCACCCACCTCG | 51366 |
rs761956858 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102394633 | TTTTTTCCCAATAAC[A/T]GTGAGGCATTTGAAC | 51366 |
rs761960657 | snp | A/G | 3.32939e-05 | 0.00407993 | intron-variant | UBR5 | GRCh38.p7 | 8:102326511 | ATTCTGAAGAGAAAC[A/G]AGGTCCCTTAAGACA | 51366 |
rs761966609 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102288658 | GGCAAGATTGCACCA[C/G]TGCATTCCAGCCTGG | 51366 |
rs761968237 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102353628 | AATAACCTATGGATG[A/C]CTTTAGTATCACCAC | 51366 |
rs761971665 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102377009 | TTGGAGACTGTTGCT[C/T]AGGACAGCCCCCTCT | 51366 |
rs761981099 | snp | A/G/T | 3.35251e-05 | 0.0040941 | intron-variant | UBR5 | GRCh38.p7 | 8:102305036 | CTGTTACATTTTCAA[A/G/T]ATTGCCTAAAACTCC | 51366 |
rs762006129 | in-del | -/ACC | 2.21889e-05 | 0.00333076 | intron-variant | UBR5 | GRCh38.p7 | 8:102257750 | AATAAAATATACTAT[-/ACC]ACCAGTTGTTGTTAT | 51366 |
rs762009211 | snp | A/G | 1.68431e-05 | 0.00290194 | intron-variant | UBR5 | GRCh38.p7 | 8:102279230 | ATAAAAAGATAAAAT[A/G]TTTTGTTTTTTAGGA | 51366 |
rs762014086 | snp | C/T | 1.67295e-05 | 0.00289214 | intron-variant | UBR5 | GRCh38.p7 | 8:102311704 | GCCATTGTTGTCCTA[C/T]CACTTTTCAAAAGCA | 51366 |
rs762015312 | in-del | -/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102315693 | ACAGCAAATACTCCT[-/G]GCTGCTCCACAAATG | 51366 |
rs762017618 | snp | A/G | 6.60469e-05 | 0.00574622 | intron-variant | UBR5 | GRCh38.p7 | 8:102295555 | ACAGAATGTTGTCGT[A/G]AGGAGGGAGGCTGAA | 51366 |
rs762026677 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102353717 | GACATGGGGTACATG[C/G]GAACTCTCAGTATGA | 51366 |
rs762028797 | snp | A/C | 1.64784e-05 | 0.00287035 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102346300 | TTCATCATCCCGGCT[A/C]AGTAAATTATTTACA | 51366 |
rs762037399 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102408177 | GAAACCAGGCAACAC[G/T]TAAAAAGTTAAAAGT | 51366 |
rs762045570 | snp | C/T | 0.00054728 | 0.016533 | intron-variant | UBR5 | GRCh38.p7 | 8:102259172 | TCATTTTCCATGTAA[C/T]ATTTATTTATATTAT | 51366 |
rs762049703 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102352709 | CCTGATCAGAAATAG[C/T]ATCCAAGTACACATC | 51366 |
rs762058949 | snp | A/T | 1.65291e-05 | 0.00287476 | intron-variant | UBR5 | GRCh38.p7 | 8:102360549 | AATATAATACCTAAG[A/T]GCTAAATACATATTA | 51366 |
rs762090410 | snp | C/T | 1.65004e-05 | 0.00287227 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102259052 | ACCGCAGCCATTTAC[C/T]AAAAGCCTAAAATCT | 51366 |
rs762092454 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102396165 | TAAATACCTATTAGA[C/G]TAAGTACAAAAAAAG | 51366 |
rs762104162 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102292024 | AGTTACTGTTATATG[A/G]GAGACATGGAAATAA | 51366 |
rs762142797 | snp | A/C/G | 0.000101084 | 0.00710865 | intron-variant | UBR5 | GRCh38.p7 | 8:102275856 | TAAGGGAAGGGGTGG[A/C/G]GGGGAGAAATAATTT | 51366 |
rs762144994 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303013 | CTGACATGAAAAAAA[A/G]ATGGCAGCACTGGCA | 51366 |
rs762149365 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102355289 | GCAGGACAGGAGTGA[C/G]GACCAAGGTCTCTGG | 51366 |
rs762168155 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102293352 | AAACTATCAAACAAA[C/T]AGAAAAGATAAATGA | 51366 |
rs762189077 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102392615 | TAGATACCAAAAAAA[-/A]AAAAAAACAAAAAAC | 51366 |
rs762199888 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102402868 | GAGCCTGAACTCATG[C/G]GGAAGAAAATAAAAA | 51366 |
rs762213211 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102328798 | TTTGTATTTTTAGTA[C/G]AGATGGGTTGGCTAG | 51366 |
rs762215111 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102260155 | AACTTGGTTTTTGCA[A/G]TATTCCAACATTACT | 51366 |
rs762228154 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102340676 | ATGGTATTTACTGAT[C/G]ACTATGATAATGCTT | 51366 |
rs762249645 | in-del | -/AC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102264569 | GAATCCTAAAAACAA[-/AC]ACAGAGAAATAAGAT | 51366 |
rs762256277 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102305958 | GCTGGTCTCAAACTC[C/T]TGGGCTCAAGTGATG | 51366 |
rs762271132 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102266412 | TACTTAGGTTCAAAT[C/T]GGAAGTCTCACCTTC | 51366 |
rs762276560 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102384298 | TCTTCAAAGGTGATA[A/G]AATATTAAAGGTATT | 51366 |
rs762276992 | snp | A/G | 3.31351e-05 | 0.00407019 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295035 | TGAAACAGTCCAGCC[A/G]AATTGTGCCACTTTG | 51366 |
rs762292885 | snp | C/G | 3.34454e-05 | 0.0040892 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311889 | AGAACAGCATGAACA[C/G]CTTCAGAAGCACATA | 51366 |
rs762306173 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311450 | ATGCAATCTTTGGCC[A/G]TTGGGTAGATGGTAC | 51366 |
rs762315395 | snp | A/G | 1.64779e-05 | 0.00287031 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102276983 | ATACCTGAAAGATGT[A/G]AGAGGTGGCCCTTCA | 51366 |
rs762338149 | snp | A/T | 1.65312e-05 | 0.00287495 | intron-variant | UBR5 | GRCh38.p7 | 8:102360680 | CCTAAAAGCAAAGAA[A/T]ACAGAAAAAATTATC | 51366 |
rs762363686 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102275259 | AAAAATTCATAGAGG[A/G]TGCTAGGGAACCAAA | 51366 |
rs762394242 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102289948 | CTAACTTTTAAGAGA[C/T]CTGACATGATTTCTA | 51366 |
rs762399098 | snp | A/T | 1.67579e-05 | 0.00289459 | intron-variant | UBR5 | GRCh38.p7 | 8:102329425 | AAATACAATACTATA[A/T]ATATAAAAATTGCCA | 51366 |
rs762407277 | snp | A/G | 1.7049e-05 | 0.00291962 | intron-variant | UBR5 | GRCh38.p7 | 8:102265289 | TCCTGCTAACAGAGA[A/G]TATCAGAGAGTAAGC | 51366 |
rs762408588 | snp | A/T | 1.6492e-05 | 0.00287154 | intron-variant | UBR5 | GRCh38.p7 | 8:102329080 | TTAATCAATGCAAAG[A/T]GTTTCATACCTTGTT | 51366 |
rs762413722 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102367995 | CTCAATTTTCAGACA[A/C]ATTTTTAAAAATCCA | 51366 |
rs762414417 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102363011 | TACCCGCCACCACAC[C/T]CGGCTAATTTTTGTA | 51366 |
rs762418276 | snp | A/G | 1.66117e-05 | 0.00288194 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102281518 | TAAGCAAGGTGGCAC[A/G]TCTATAAGAACAGAA | 51366 |
rs762443424 | snp | G/T | 3.63802e-05 | 0.00426483 | intron-variant | UBR5 | GRCh38.p7 | 8:102264443 | AATTTTTGCAATTGT[G/T]AATACAATTAGGTTC | 51366 |
rs762444285 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102401661 | TCCTACCAGGAATCG[C/T]CTCAGGTAGCAGGAA | 51366 |
rs762456546 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102296759 | TTATACATAAACTGA[C/T]TTAAACAAGGGAAAC | 51366 |
rs762460355 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102291230 | GCAATTTGGCAGACT[A/G]TGCAGAGAAACCACT | 51366 |
rs762464454 | snp | C/T | 4.96298e-05 | 0.00498121 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102297485 | CTCTGCTCCAGTCCA[C/T]GTAAAACTGCAAGTG | 51366 |
rs762484198 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102276264 | GGCTTCTTCACCACA[A/G]TGACAGTTCTCCTGA | 51366 |
rs762506321 | snp | A/T | 5.18211e-05 | 0.00508998 | intron-variant | UBR5 | GRCh38.p7 | 8:102285102 | TTAAGTTGGGGACGT[A/T]CTGTATATATGAAGA | 51366 |
rs762522335 | snp | G/T | 6.67256e-05 | 0.00577567 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102275827 | TAAAGCTACACTGTG[G/T]CCTGTAAGAAGTTTA | 51366 |
rs762525549 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102387355 | CTCACAGTCCATTAG[A/G]TTTTTAAAATATCTC | 51366 |
rs762575301 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102383154 | GGTAGGAGGAAGCCG[A/G]AAATGAACAGGTCAA | 51366 |
rs762594327 | snp | G/T | 0.000132466 | 0.00813728 | intron-variant | UBR5 | GRCh38.p7 | 8:102360232 | TGAAGACCAACATTT[G/T]TTACAACCCTGTTAT | 51366 |
rs762654675 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102388525 | GTTCTTCTTTTTTTC[A/G]TATCAGAAGAGTAAC | 51366 |
rs762677495 | snp | A/C | | | intron-variant, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102276906 | AGTCTATAAATGGTA[A/C]CTAGACATGGATATA | 51366 |
rs762679481 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102400110 | TTTGCATCTTCTTTT[G/T]AGTCTGTAATTATTT | 51366 |
rs762685448 | snp | A/C/T | 3.48835e-05 | 0.00417621 | intron-variant | UBR5 | GRCh38.p7 | 8:102265070 | TGAAATGTTTTAAAA[A/C/T]ATTCAAACCCAAGAT | 51366 |
rs762689321 | snp | A/T | 1.95681e-05 | 0.00312789 | intron-variant | UBR5 | GRCh38.p7 | 8:102329213 | ATTCTTTGAAAGCAT[A/T]AAAAAAAATTACTAT | 51366 |
rs762701761 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102371857 | CTCCCAAAGTGCTGG[A/G]ATTACAGGTGTGAGC | 51366 |
rs762708715 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102263330 | GGAGGTGGAGGTTGC[A/G]GTAAGCCGAGATCGT | 51366 |
rs762712479 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102398876 | TATTTACAAACTATC[C/T]ACCTGATAAGGGATT | 51366 |
rs762712634 | snp | C/T | 3.31066e-05 | 0.00406844 | intron-variant | UBR5 | GRCh38.p7 | 8:102313775 | TTATAATTCTGTTAG[C/T]AATTAAGTTTTAGAT | 51366 |
rs762715443 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102347926 | TATTTCTAATCACAA[C/T]TATAAAATGAACACA | 51366 |
rs762723102 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102365016 | TTTAAAGGATCTTCA[-/T]ACAATGTTTACGATA | 51366 |
rs762740682 | snp | C/T | 1.64808e-05 | 0.00287057 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102312428 | TGTTCTGACAGTTAG[C/T]ATTACTGGAGGTTCC | 51366 |
rs762757561 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102316059 | AAGTCTATAAATCTT[C/T]TTTAAAAAACCAAGA | 51366 |
rs762775346 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102397022 | GGTCTCATTTTTAAG[C/T]ATCTCTGTGAGAACA | 51366 |
rs762790151 | snp | A/G | 2.20631e-05 | 0.00332131 | utr-variant-3-prime, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102254267 | TCTACAAAATTTGCT[A/G]GTAATATTACACAGC | 51366 |
rs762790619 | snp | C/T | 1.71088e-05 | 0.00292474 | intron-variant | UBR5 | GRCh38.p7 | 8:102294933 | GCAAAGAAGAGTACT[C/T]GAAAAACATACTTTT | 51366 |
rs762791296 | snp | A/G | 0.000251132 | 0.0112028 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102304013 | TGGTTTTTTCCTCCA[A/G]TTAAAGTTTCCTGGT | 51366 |
rs762815076 | snp | A/T | 1.69338e-05 | 0.00290974 | intron-variant | UBR5 | GRCh38.p7 | 8:102346402 | AACTTGGGCCTGAAA[A/T]AAAAAATAAAAAGAA | 51366 |
rs762816444 | snp | C/T | 1.65996e-05 | 0.00288089 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102286378 | CTGGTGTAGATGTAC[C/T]GGAAGGGGCTGTACT | 51366 |
rs762824834 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102297747 | AGTGATATACAAAGA[A/T]GACATGCAAAGAAAT | 51366 |
rs762827661 | snp | C/T | 0.000147721 | 0.00859295 | intron-variant | UBR5 | GRCh38.p7 | 8:102271269 | AAATCAGAAATATAC[C/T]GTATTTAGATGAATG | 51366 |
rs762829146 | in-del | -/T | 3.3592e-05 | 0.00409815 | intron-variant | UBR5 | GRCh38.p7 | 8:102346207 | AGAGCACTCCAGAAA[-/T]GAGAAAAACATGACG | 51366 |
rs762842220 | snp | A/G | 1.65173e-05 | 0.00287374 | intron-variant | UBR5 | GRCh38.p7 | 8:102295565 | GTCGTGAGGAGGGAG[A/G]CTGAAAAGCTACTCA | 51366 |
rs762844114 | snp | C/T | 3.42454e-05 | 0.00413782 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102304218 | GTTTTAGAACTAATA[C/T]ACTGAGTATGTATAG | 51366 |
rs762871863 | snp | C/T | 3.29815e-05 | 0.00406075 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102279139 | ATGGAGTCTGAACGT[C/T]GGAAAAATGGATGGT | 51366 |
rs762901295 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102265010 | GCCACCGCACCCAGC[A/G]TACATACATTTTAAA | 51366 |
rs762911466 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102256302 | GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAC | 51366 |
rs762911518 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102354469 | GTAGCTCAAATCAAC[G/T]AAAAGCAGCTTATAC | 51366 |
rs762921785 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102366611 | ATTTAAGATAGTTTC[A/C]CATATAACTCTTAAA | 51366 |
rs762937076 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102407690 | ACCCAGGAGGTGGAC[A/G]TTGCATTGAGCCGAG | 51366 |
rs762937671 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102376046 | GGCAAAATTAGTGCC[-/A]AGACTGGTCCTACCG | 51366 |
rs762967272 | snp | C/T | 1.65405e-05 | 0.00287576 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295639 | AATCCCACTTGCCTG[C/T]TGTTTGGCAGAGTAA | 51366 |
rs762971505 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102396294 | CTCTACAGTCACACA[C/G]ATTCAAGGCTGAAAT | 51366 |
rs763006377 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102272322 | GAAAAACTAGTACAA[C/T]CACAAACATTTATCA | 51366 |
rs763022086 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102264112 | ATTTACCAATCACTT[-/A]ACTATTTGCCAGGTA | 51366 |
rs763032580 | snp | C/T | 1.65141e-05 | 0.00287346 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102293658 | TTCCACTGAAAATAA[C/T]TCTTCACTGCCCTGC | 51366 |
rs763048136 | snp | A/T | | | intron-variant, downstream-variant-500B, nc-transcript-variant | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102252081 | AAATAGTGAAATCAT[A/T]CCTTTAAAATACCCT | 51366 |
rs763057446 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102270799 | GCTGGAATTACAGGC[A/G]TGAGCCACCGCATGT | 51366 |
rs763059400 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102286033 | TTTGGCAGTATCTAC[A/C]GACATTCTTGGTTAT | 51366 |
rs763071754 | snp | C/T | 3.44039e-05 | 0.00414738 | intron-variant | UBR5 | GRCh38.p7 | 8:102261111 | AGACACAAATAGCCT[C/T]ATTGGATCACACAAC | 51366 |
rs763074467 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102259523 | ACAAACTCAAAAGCT[A/G]GATGCTTACTGAGAA | 51366 |
rs763083603 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102374197 | TCAATATTACTGAAA[C/T]GTATTTTTCATCCTT | 51366 |
rs763086375 | snp | C/T | 3.31691e-05 | 0.00407228 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102346929 | GCTCCTCTGGAATGA[C/T]AGATGCTGGAATAAC | 51366 |
rs763087454 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102260319 | GGCTGGTTGTGCAGA[C/T]AGAAAATGCCCATGG | 51366 |
rs763088639 | snp | C/T | 5.16276e-05 | 0.00508046 | intron-variant | UBR5 | GRCh38.p7 | 8:102293562 | CAAACACGACATTTC[C/T]AGAGAAGGATTAATC | 51366 |
rs763097929 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102384518 | CTAATGTGGGCAACA[C/T]AATGAGACCCCGTCT | 51366 |
rs763100378 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102316676 | CCAAAAAACGTTTAC[C/T]AATTCTTTACAGATA | 51366 |
rs763127951 | in-del | -/TTAA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102301196 | AATTGCAATTATTAT[-/TTAA]TTAATTGAGGATAAA | 51366 |
rs763139033 | snp | G/T | 1.6483e-05 | 0.00287076 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102272627 | GTATAAAAACTTCGT[G/T]CTACACCACTGCCCT | 51366 |
rs763153627 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102353714 | CTAGACATGGGGTAC[A/G]TGGGAACTCTCAGTA | 51366 |
rs763154163 | snp | C/T | 5.08177e-05 | 0.00504046 | intron-variant | UBR5 | GRCh38.p7 | 8:102261291 | AGTGCTATTTAAAGG[C/T]AATTTTGTCAAAGCA | 51366 |
rs763165375 | snp | C/T | 1.65449e-05 | 0.00287614 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102298946 | TCGATCCTTGGATTC[C/T]ACTACAGATGGCTCT | 51366 |
rs763166279 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102397347 | CCAGCCATCTTTGTA[C/T]TCCAGTGTATACACA | 51366 |
rs763170792 | snp | A/G | 1.64974e-05 | 0.00287201 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311759 | AGTGAAAATGGCTAC[A/G]TTCCTCTCATTCTGA | 51366 |
rs763172883 | snp | A/G | 1.6543e-05 | 0.00287597 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102326631 | CTAGCTTTCTCTAAC[A/G]TTTTCTTCCTTTGAC | 51366 |
rs763183344 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102367706 | TGCACTCTGTATTAC[G/T]ACAAACATTAGGAGC | 51366 |
rs763183966 | snp | C/T | 6.64971e-05 | 0.00576577 | synonymous-codon, nc-transcript-variant, intron-variant | UBR5 | GRCh38.p7 | 8:102285267 | AGAACCATAACGTAA[C/T]TGAGCTTCAGTAGAA | 51366 |
rs763195485 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102356909 | GGCCAACACCACAGT[A/G]ACAACTGATTCAGAC | 51366 |
rs763267203 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102344382 | GCAGTGGTACCACCT[C/G]AGCTCACTGCAAGCT | 51366 |
rs763289724 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102331688 | CAAATCAATGCTCAA[C/T]GTACGTAATCAGTCC | 51366 |
rs763290122 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102268498 | TGAGAGCCACCGCAC[C/T]CGGCCTTATCTTCCT | 51366 |
rs763293810 | snp | C/T | 1.65269e-05 | 0.00287457 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102361175 | CACACTGTTTAATAG[C/T]AGCCTGTTCCAATAC | 51366 |
rs763298713 | snp | C/T | 3.3987e-05 | 0.00412218 | intron-variant | UBR5 | GRCh38.p7 | 8:102311901 | ACACCTTCAGAAGCA[C/T]ATAAATGAGAAGAAA | 51366 |
rs763304275 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102391575 | TATATACACACATAT[-/T]TTGCAAATATAGCAA | 51366 |
rs763311849 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102330049 | TCATTCGTTCACTTT[C/T]ATGTTGACATACATG | 51366 |
rs763314944 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102363633 | GTTCACTGGCATGCA[A/G]CTAAACTCATTCATT | 51366 |
rs763325182 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102268312 | ACCTCGTGATCCACC[C/T]GCTTTGGCCTCCCAA | 51366 |
rs763350920 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102370772 | ACCATTCTTTCTACT[C/T]TATACCTCTATGAGA | 51366 |
rs763364004 | in-del | -/T | | | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102413468 | AACGGAAAATTATTA[-/T]TTTTTTTTTTTTTTT | 51366 |
rs763365990 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102392617 | GATACCAAAAAAAAA[A/C]AAAAACAAAAAACAA | 51366 |
rs763376819 | snp | C/G | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102277018 | CAGTAAGTCCTATTT[C/G]TGCTAGTAAGCTACT | 51366 |
rs763379893 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102343515 | ATTAGCTATTCCATA[A/T]GGTTCAAACTAAAAG | 51366 |
rs763384574 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102404420 | AATAATTTCTTATAG[C/T]CAAGTTCAATTGACT | 51366 |
rs763403510 | snp | A/G | 1.64866e-05 | 0.00287106 | intron-variant | UBR5 | GRCh38.p7 | 8:102287413 | ATAAGCAAGAAAGTA[A/G]TTGGGATAAGGCAAC | 51366 |
rs763411995 | in-del | -/AA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102296777 | AAACAAGGGAAACGT[-/AA]GTAACCTCATGCTTT | 51366 |
rs763412573 | snp | G/T | 1.64798e-05 | 0.00287047 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102342525 | ACTGGACTTTGAACA[G/T]GTGTATTCTTCTTAT | 51366 |
rs763424832 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102375091 | TTTGGCCGGGCACGG[C/T]GGCTCACACCTGCAA | 51366 |
rs763433246 | in-del | -/CAAAA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102257927 | CTGACTCAATATGAC[-/CAAAA]CAAATGAACCACCAG | 51366 |
rs763436773 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102294941 | GAGTACTTGAAAAAC[A/G]TACTTTTCATGTACT | 51366 |
rs763439221 | snp | C/T | 1.66358e-05 | 0.00288402 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102299475 | GTGGAGGTGCTTGGT[C/T]CTTGACCAGTACCGG | 51366 |
rs763488757 | snp | G/T | 1.76871e-05 | 0.00297375 | utr-variant-3-prime, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102254301 | ACACACTTTTTATAC[G/T]CTACACAAAACCAAA | 51366 |
rs763489024 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102312940 | GACTTTTTTAAGTTA[C/T]TTGATTTTAACAAAT | 51366 |
rs763490290 | snp | C/T | 3.31906e-05 | 0.0040736 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295309 | CTTGGAGGCTCTAAA[C/T]CATGATCTGGCATAT | 51366 |
rs763499794 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102350366 | CAGTATGGGTATGGG[C/T]ATAACGACAAAAAAG | 51366 |
rs763519776 | in-del | -/GGACAAGAA | 1.64773e-05 | 0.00287026 | cds-indel, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102286526 | GTCTCCTGTTCTATG[-/GGACAAGAA]TCGTCACTCTGACTA | 51366 |
rs763524044 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102379489 | CAATTCACACTTGGA[A/C]CATACAGTTCCTTTG | 51366 |
rs763525200 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102267446 | TCAATATTGTACATT[A/G]GTTGCATTCAACAGA | 51366 |
rs763528288 | snp | A/G | 1.64901e-05 | 0.00287137 | intron-variant | UBR5 | GRCh38.p7 | 8:102287406 | CCTTAGCATAAGCAA[A/G]AAAGTAGTTGGGATA | 51366 |
rs763536008 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102253757 | TGCAGTCAAACCGCA[A/G]TAAAAGTGGTTTTTA | 51366 |
rs763539428 | snp | G/T | 2.15845e-05 | 0.00328509 | intron-variant | UBR5 | GRCh38.p7 | 8:102254556 | TTTAACTCTTAACTC[G/T]GGCAGTATATACACA | 51366 |
rs763564662 | in-del | -/TAATATAAAGTTCTCAACCAGGGGAAATCTGACCCCCA | 1.64775e-05 | 0.00287027 | frameshift-variant, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102286527 | TCTCCTGTTCTATGT[lengthTooLong]CGTCACTCTGACTAC | 51366 |
rs763575548 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102401851 | AAACACAATCACTTA[A/T]GGAAAACACCTAAGG | 51366 |
rs763652408 | in-del | -/T | 0.000131863 | 0.00811875 | frameshift-variant, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102277121 | CTGTTCTTCCCCTTC[-/T]TTTTTTTGCCGGTTT | 51366 |
rs763654154 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102252539 | AGAGGTTAAGGTGAT[A/G]TATAAATTTTATATC | 51366 |
rs763657381 | snp | A/G | 1.81408e-05 | 0.00301165 | intron-variant | UBR5 | GRCh38.p7 | 8:102296869 | TTATAATATTAAACT[A/G]AAGAAAACTAGAATT | 51366 |
rs763658265 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102267397 | AGAACACCAATAAAT[G/T]CACTGTTTACTCCAG | 51366 |
rs763659048 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102286958 | CTGAGGTGGGAGGAC[G/T]GCTTGAGCTCAGGAG | 51366 |
rs763663037 | snp | A/G | 1.65647e-05 | 0.00287786 | intron-variant | UBR5 | GRCh38.p7 | 8:102313945 | AAAATGGTAAGTACC[A/G]AAAAGAAAATGTAAA | 51366 |
rs763665820 | snp | C/T | 1.94131e-05 | 0.00311548 | intron-variant | UBR5 | GRCh38.p7 | 8:102254539 | AATTTAACAGGTTAA[C/T]ATTTAACTCTTAACT | 51366 |
rs763668944 | snp | A/T | 3.3054e-05 | 0.00406521 | intron-variant | UBR5 | GRCh38.p7 | 8:102305073 | AGACCTTGCTATAGT[A/T]CTTAATCTCACCCTC | 51366 |
rs763670948 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102317201 | TCAAGGAAAGGGGTG[A/G]CAGACAGCACCTGGA | 51366 |
rs763698188 | snp | A/G | 1.64781e-05 | 0.00287033 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102281354 | CTTAATCCAGTATAT[A/G]AGTGCTTGAAAAACA | 51366 |
rs763708266 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102368229 | AACTCCCCATTTTGT[C/G]CTTAATTTTTTTCAT | 51366 |
rs763729735 | snp | C/T | 4.94303e-05 | 0.00497119 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102346984 | CCCAGACCCTCGATC[C/T]CGTCCTGTCCGAATA | 51366 |
rs763729809 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102324833 | ATGTTAAGACATGAA[C/T]ATTTTACTTGTTCTG | 51366 |
rs763753963 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102382536 | ACACACAAAAAGAAA[A/G]CACAAACCCTGATTA | 51366 |
rs763754133 | snp | C/T | 1.65669e-05 | 0.00287805 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295704 | ATCAAGACGAGCAGA[C/T]TTCTGTCCAGCAATA | 51366 |
rs763770305 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102369370 | ACTTTGAATAACTCA[A/G]GTATGATTTTGTCAT | 51366 |
rs763782870 | snp | A/T | 1.7668e-05 | 0.00297215 | intron-variant | UBR5 | GRCh38.p7 | 8:102347143 | AACAATCATTCTGAT[A/T]GCTTGGTTTTCATTA | 51366 |
rs763783981 | snp | A/T | 1.67019e-05 | 0.00288975 | intron-variant | UBR5 | GRCh38.p7 | 8:102272807 | AGTCAAAAAGTAGTA[A/T]ATTCAATGTTGGAAA | 51366 |
rs763789006 | snp | C/G | 0.000135323 | 0.00822453 | intron-variant | UBR5 | GRCh38.p7 | 8:102326696 | AAATTGGTCAAATAA[C/G]CAGTAAAACAGCCCA | 51366 |
rs763793050 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102380267 | CACATGGTGGTACAC[A/G]CCTGTAGTCCCAGCT | 51366 |
rs763801685 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102363967 | CCTGGTGAGACCCCT[-/A]AACCACATCTGAAAT | 51366 |
rs763820621 | snp | G/T | 1.64773e-05 | 0.00287026 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102272580 | CTAGATTTGGCAATT[G/T]TTCATTTGATAAAAA | 51366 |
rs763845568 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102294401 | TATGAAATCAGAAGA[A/G]GAAAACATAAACTCA | 51366 |
rs763848908 | snp | A/G | 1.64868e-05 | 0.00287109 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102272684 | TTTACTCTGTGTACA[A/G]CCATTGGTGTAGTAG | 51366 |
rs763862244 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102260714 | TACAGTAGGACAAAG[A/G]ACTAAGATATATTAT | 51366 |
rs763895002 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102306145 | TATAGAACATATCAT[C/T]AGCTTTCTGACAAAT | 51366 |
rs763900847 | in-del | -/T | 1.75246e-05 | 0.00296007 | intron-variant | UBR5 | GRCh38.p7 | 8:102346435 | GCTATGGTAATTTTC[-/T]TTTGATTAAATTCTT | 51366 |
rs763909800 | snp | A/T | 1.65828e-05 | 0.00287943 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285539 | CTGCATCTTGGTAAG[A/T]CAATTTCACAGCTGC | 51366 |
rs763909937 | snp | A/G | 1.64863e-05 | 0.00287104 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102327775 | TCCAGCTGAGCGCAG[A/G]TGTAAAGGGCACAGC | 51366 |
rs763924267 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102307441 | AAGCTAAGCTAAGAA[C/T]GAGTCTGGGTGTCTA | 51366 |
rs763970037 | snp | A/C | 3.53763e-05 | 0.00420558 | intron-variant | UBR5 | GRCh38.p7 | 8:102261878 | CAGTTTAACCAAATT[A/C]TCTTGCCAGAATCAG | 51366 |
rs763981304 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102335635 | CACACTGCAACCACC[A/G]TCCCCCAAGTTCAAG | 51366 |
rs763986573 | snp | A/G | 3.29951e-05 | 0.00406159 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102262005 | TGAACTCTGAGACGC[A/G]AGGATTAGTTGCCGC | 51366 |
rs763988629 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102397485 | ATCACCTGAGGTCAG[A/G]AGTCAGGAGTTCGAG | 51366 |
rs763988731 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102411525 | CAAATTTAATAATAA[C/T]AACAATAATCATGGC | 51366 |
rs763990115 | snp | C/G | | | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102299518 | TAAGAGATCCCACAG[C/G]GGGGGCCAGGATAAA | 51366 |
rs764038897 | snp | C/T | 1.65941e-05 | 0.00288041 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102312198 | AAGCTTTTTAGGAGT[C/T]CTTTGGAAACAGTCG | 51366 |
rs764048914 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102308220 | ACTTCCTCTATCAGA[A/G]GAGACATCTTAAACT | 51366 |
rs764051872 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102273844 | GGAGGAGGTATGTAA[C/T]TAATACATACATATG | 51366 |
rs764060438 | snp | C/T | 1.65594e-05 | 0.0028774 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102300033 | GGTCAGGAACCCAAC[C/T]AGGGGGAGCTATGGG | 51366 |
rs764068978 | snp | G/T | 1.67307e-05 | 0.00289224 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285747 | ACTCCGGCGTAAGTT[G/T]GAAGGATCAATATAA | 51366 |
rs764071253 | snp | C/T | 1.65154e-05 | 0.00287358 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102277175 | ATTGGCAGCATAAGA[C/T]ATTTTTGTTGGAAGA | 51366 |
rs764083108 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102405046 | TTTAACATGTTAGAA[C/T]CCAATCAGCTTTATT | 51366 |
rs764097470 | snp | A/C | 4.98799e-05 | 0.00499374 | intron-variant | UBR5 | GRCh38.p7 | 8:102270003 | GCAAAAAAATAACAC[A/C]GCCAGTTAAGAGGTA | 51366 |
rs764102879 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102393365 | ACGGAAACAACAGGC[A/G]GTGGTTCACACTAGT | 51366 |
rs764105458 | snp | C/T | 1.70327e-05 | 0.00291823 | intron-variant | UBR5 | GRCh38.p7 | 8:102342728 | GATAAAAGTAAGCCA[C/T]TCTCTAGTAAAGACC | 51366 |
rs764107695 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102376767 | CCTAGGCTTCCCAAA[A/G]TGCTGGGATTACGGG | 51366 |
rs764109176 | snp | C/G | 4.99313e-05 | 0.00499632 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102361200 | CAATACATTCAAAGG[C/G]GGGTGGCTGAGAGAT | 51366 |
rs764119114 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102331981 | TTTAAATGTGTAAAT[A/C]TCATATCTCCAGACT | 51366 |
rs764120546 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102313440 | TTTTTCAGTACTCTG[A/G]AAGAATTTTAAATGT | 51366 |
rs764156963 | snp | C/G | 1.84194e-05 | 0.0030347 | intron-variant | UBR5 | GRCh38.p7 | 8:102323268 | ATGCAGAGCAAACAA[C/G]GAACTGGTGTCAAAG | 51366 |
rs764157841 | snp | C/T | 6.60273e-05 | 0.00574537 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102278839 | ACCTCTAGGCAGTTT[C/T]TATCCACTGTAACCT | 51366 |
rs764166124 | snp | C/T | 1.74705e-05 | 0.00295549 | intron-variant | UBR5 | GRCh38.p7 | 8:102361650 | CAAAACATTAACAAA[C/T]CACGTGTACAGATCT | 51366 |
rs764179724 | snp | A/G | 4.62802e-05 | 0.00481019 | intron-variant | UBR5 | GRCh38.p7 | 8:102257754 | AAAATATACTATACC[A/G]GTTGTTGTTATTATC | 51366 |
rs764187340 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102284209 | CATAACAAATACATA[A/G]ATATATATTTTATTT | 51366 |
rs764196752 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102394922 | ATTAACAAGGTATCC[A/T]TTTCTACAAGAACAT | 51366 |
rs764221348 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102268707 | TATGGCCTTTGCCAG[C/G]AGGGTATTCTGATAA | 51366 |
rs764230804 | in-del | -/AC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102392482 | TAAAGCTACACAAAC[-/AC]ACACACACACACCTC | 51366 |
rs764262005 | snp | A/G | 1.64906e-05 | 0.00287142 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102270132 | GCTAGGATTCCCTTC[A/G]GAGGCTGGTCTAAAG | 51366 |
rs764307865 | snp | C/T | 1.71443e-05 | 0.00292777 | intron-variant | UBR5 | GRCh38.p7 | 8:102345559 | CTCTATAAACAGAAA[C/T]AAACATCACTGCAGC | 51366 |
rs764309724 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303800 | AGAATGATGAATTTA[C/G]AACAAATTGAAAGAA | 51366 |
rs764328702 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102339223 | ATCATTAAAATAATT[G/T]TATTGGCTTACAAAA | 51366 |
rs764366022 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102351877 | TCCCAGCTACTTAGA[A/G]GGCTGAGGCAGGAGG | 51366 |
rs764372601 | snp | A/G | 1.64838e-05 | 0.00287083 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295442 | TGTTTTTCGGTTACG[A/G]TCTTCCCTGATTCGA | 51366 |
rs764390118 | snp | C/T | 1.71575e-05 | 0.0029289 | intron-variant | UBR5 | GRCh38.p7 | 8:102285110 | GGGACGTTCTGTATA[C/T]ATGAAGAATTTCATA | 51366 |
rs764401818 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102314634 | TAGAGATACAAATTA[C/T]ATAAAAAGATGTAAA | 51366 |
rs764407037 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102297389 | CTGAAAACTGTAAGT[C/G]TAGTGATAGTCATAG | 51366 |
rs764411261 | snp | A/C | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311480 | CCATTTCCATCTCGA[A/C]GAATAATGGGAGATT | 51366 |
rs764412292 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102393593 | ATGAGCTGAGATCAC[A/G]CCACTGCACCCCAGT | 51366 |
rs764422707 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102304874 | ATTACATATCCAGTT[A/T]GTATATATCATATAG | 51366 |
rs764438707 | snp | C/T | 3.30633e-05 | 0.00406578 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102323406 | CATATTCCAAACTGA[C/T]TCCATTAAGACACCA | 51366 |
rs764454872 | snp | G/T | 0.000134996 | 0.00821461 | intron-variant | UBR5 | GRCh38.p7 | 8:102281541 | GAACAGAAAGGAAAA[G/T]GTTTATTAGAAGAAT | 51366 |
rs764468983 | snp | A/T | 1.64811e-05 | 0.00287059 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102288259 | GCCACACCCTCCACC[A/T]CCTCAACCTAAATCC | 51366 |
rs764483041 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102383396 | ATACACCCAGAATCG[G/T]CGTGGGAGGGAGAAG | 51366 |
rs764487128 | snp | A/C | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102289501 | TTCTTCATCTCTGCC[A/C]CGAACGGGCTGTGAC | 51366 |
rs764493151 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102343021 | ATAAATTCAATTTAC[-/A]TATCAGAAAATATAC | 51366 |
rs764495769 | snp | A/C | 1.65053e-05 | 0.0028727 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102259039 | GCACATTGACTTCAC[A/C]GCAGCCATTTACCAA | 51366 |
rs764526524 | snp | C/G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102387889 | CAGAACTTATTCCTT[C/G/T]CCCTCTGTTAGACCT | 51366 |
rs764526973 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102327524 | TGTTTCTACTTTATA[C/G]TTTCATAAAACTTAT | 51366 |
rs764539795 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102299331 | TAATTCAGAGAATTA[C/G]ATGTTTTTCAAGCAA | 51366 |
rs764553176 | in-del | -/TTGTG | | | intron-variant | UBR5 | GRCh38.p7 | 8:102264235 | ACCCCCCAGCCCCAC[-/TTGTG]TTATCTACTCTGCTA | 51366 |
rs764572851 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102382508 | GAAATATAACACAAG[A/G]GTAGAGAGAGACACA | 51366 |
rs764584874 | snp | A/C | | | intron-variant, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102276955 | GAACAATAAAAACAA[A/C]GGGTCTTAGCAAATA | 51366 |
rs764587428 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102397103 | AAGACTCTCTGCAAG[A/G]CTCAGATATCCTATC | 51366 |
rs764591045 | snp | C/T | 2.55157e-05 | 0.00357172 | intron-variant | UBR5 | GRCh38.p7 | 8:102298510 | ATAAGAAAAATTATA[C/T]GTAAAAATATTAATT | 51366 |
rs764611761 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102257565 | TTACAAACTTAAAAG[A/G]CCATCATACATGGTA | 51366 |
rs764625195 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102289810 | TGATGCACATTATTT[A/G]TATGAGTCCATCCCA | 51366 |
rs764627199 | in-del | -/GC | 1.73978e-05 | 0.00294934 | intron-variant | UBR5 | GRCh38.p7 | 8:102261908 | GAAAAGTGTATATTT[-/GC]TTTACCTGTCCTCCA | 51366 |
rs764630878 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102358722 | CATGAAAACACAAAC[G/T]CAAAGAAAGTAATCA | 51366 |
rs764631855 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102400360 | CTCGCTAATCTATAA[C/T]CTCACTCTTCTCCAA | 51366 |
rs764634598 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102363812 | ATTCCAGACAATTAT[C/T]TGTAAAACTAAAGTA | 51366 |
rs764661308 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102328672 | GCTCACTGCAACCTC[C/T]ACCTCCCAGGTTCAA | 51366 |
rs764670903 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102369727 | ATCTTATGCTCAAAG[A/G]TATAGATTTAATACA | 51366 |
rs764695513 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102309744 | GTAAGTGCACTATGT[A/G]ATGTTTGTACAACAA | 51366 |
rs764767117 | in-del | -/TTT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102335201 | CTTATATGTGAAGTC[-/TTT]TTTTTTTTTTAAAGG | 51366 |
rs764778826 | snp | C/T | 3.29902e-05 | 0.00406128 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311322 | CCATGATGATAACAG[C/T]AGCTTTCTTTTTGAT | 51366 |
rs764806126 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102322955 | TGGGGTGGGGGGAGG[G/T]GGAGGGATAGCATTA | 51366 |
rs764813126 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102288721 | AAAAATTATACCCAC[A/G]GATCCCAAAGTTCAT | 51366 |
rs764815297 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102385523 | GACCTCTTCCAGAAT[G/T]TCTTGACTCTGTTTT | 51366 |
rs764816360 | snp | A/G | 1.66599e-05 | 0.00288611 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102296932 | ACCCTTGCACATTCC[A/G]TACAACAACACAGTG | 51366 |
rs764819050 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102326376 | TACTAATACTGAACC[A/G]CAATCTATACAGTAT | 51366 |
rs764820607 | snp | A/G | 2.04773e-05 | 0.00319973 | intron-variant | UBR5 | GRCh38.p7 | 8:102257740 | TGAAGAATGTAAATA[A/G]AATATACTATACCAG | 51366 |
rs764823601 | snp | A/G | 1.94778e-05 | 0.00312066 | intron-variant | UBR5 | GRCh38.p7 | 8:102275474 | TTTTAAAATTTATAT[A/G]AATAGCATACTACAG | 51366 |
rs764829660 | snp | C/T | 1.6566e-05 | 0.00287797 | intron-variant | UBR5 | GRCh38.p7 | 8:102360033 | GAAGATGATACAGAC[C/T]ATCTGTAAGATGGTG | 51366 |
rs764837273 | snp | A/G | 1.65195e-05 | 0.00287393 | intron-variant | UBR5 | GRCh38.p7 | 8:102275628 | TTAGGATCTTAAAAA[A/G]AAAAAAATGCATGAC | 51366 |
rs764839641 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102324954 | GCAATTTAGTGTCAA[G/T]CTTTTTTATTTAAAG | 51366 |
rs764850751 | in-del | -/AAAAAAAAC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102392615 | TAGATACCAAAAAAA[-/AAAAAAAAC]AAAAAACAAAAAACA | 51366 |
rs764853595 | snp | A/C | 3.31439e-05 | 0.00407073 | intron-variant | UBR5 | GRCh38.p7 | 8:102329046 | GAAAAAAAGAAAACA[A/C]GAATTAAAGCATGAA | 51366 |
rs764867858 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102350140 | AGTGAGCCATCCATG[-/T]TTGTGCCACTGCACT | 51366 |
rs764878642 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102360450 | TTAAAATTAAACTAG[-/A]AAAGCAATAGTTTCA | 51366 |
rs764879457 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102337799 | GATTCTTGTTGGAAG[A/T]AGGTTGGTATAAACA | 51366 |
rs764889684 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102270664 | AGCTGGGATTACAGG[A/C]ATGCGCCACCACACC | 51366 |
rs764926956 | snp | C/G/T | 7.4226e-05 | 0.00609168 | intron-variant | UBR5 | GRCh38.p7 | 8:102264439 | AGAAAATTTTTGCAA[C/G/T]TGTGAATACAATTAG | 51366 |
rs764936578 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102370626 | ACATACAACAAATTA[C/T]TGATAACTATAGTCA | 51366 |
rs764955163 | snp | A/T | 1.68556e-05 | 0.00290302 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102293726 | CAGTTGGACGAGCAA[A/T]CCCCATTCTGACAGG | 51366 |
rs764965867 | snp | A/C | 3.29701e-05 | 0.00406005 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102278897 | ATGAAGAATAAAGAC[A/C]CTGACTTGGACGGCC | 51366 |
rs764981201 | snp | A/G | 1.65089e-05 | 0.00287301 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102262019 | CGAGGATTAGTTGCC[A/G]CAAACTCTCATACAT | 51366 |
rs764982354 | snp | C/T | 3.36259e-05 | 0.00410022 | intron-variant | UBR5 | GRCh38.p7 | 8:102297655 | AGGAAAGGACTTAAT[C/T]AGCCATCCATTTTCT | 51366 |
rs764986524 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102308457 | GACCACATATATGAC[C/T]GTGGTACTATAAGAT | 51366 |
rs765003088 | in-del | -/T | 1.65278e-05 | 0.00287466 | intron-variant | UBR5 | GRCh38.p7 | 8:102313936 | ACAACAACAAAATGG[-/T]TAAGTACCAAAAAGA | 51366 |
rs765043340 | snp | A/G | 1.66131e-05 | 0.00288206 | intron-variant | UBR5 | GRCh38.p7 | 8:102293904 | ATAAATCACTATCAC[A/G]AAAACAGAGTGAAAA | 51366 |
rs765044763 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102345602 | AGCAACTGTAGACTG[A/C]TGAAAGAGCTCTAAA | 51366 |
rs765057532 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102388496 | ACTAATTAAACGGAT[G/T]ATGAAGCCGAGTGGT | 51366 |
rs765061645 | snp | G/T | 1.65192e-05 | 0.00287391 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102294042 | ATTGTCACAGCAATA[G/T]CTTCTTCTCTACGTC | 51366 |
rs765080818 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102334263 | TTCCTCTAGACTAGA[C/T]AGAAATAGATCCAGA | 51366 |
rs765101628 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102346848 | AACCCACCATATTCA[G/T]TAAAACCTCACCTTG | 51366 |
rs765110610 | in-del | -/TAACTA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102306271 | CAAAGTTGTTCATTT[-/TAACTA]TAACTAGAAAAAAGC | 51366 |
rs765110997 | snp | C/G | 1.65157e-05 | 0.0028736 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102300047 | CTAGGGGGAGCTATG[C/G]GGGGTGAAACTGGAT | 51366 |
rs765133167 | snp | A/C/G | 6.99171e-05 | 0.00591222 | intron-variant | UBR5 | GRCh38.p7 | 8:102361656 | ATTAACAAACCACGT[A/C/G]TACAGATCTTTTGTA | 51366 |
rs765136449 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102309505 | TACCACTCACTCACT[A/G]ACTTACCCAGAGCAA | 51366 |
rs765141720 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102284684 | AAACTCATCATAAAC[A/G]CATAAAGTCTAAACG | 51366 |
rs765160142 | snp | C/T | 1.67654e-05 | 0.00289524 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102304008 | GTACTTGGTTTTTTC[C/T]TCCAATTAAAGTTTC | 51366 |
rs765164666 | in-del | -/AC | | | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102414278 | GTCTGTTAATGAATT[-/AC]ACACACACACACACA | 51366 |
rs765171323 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102396908 | AGACGGAGTTTCACT[C/T]TGTTGGCCAGGATGG | 51366 |
rs765174874 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102257765 | TACCAGTTGTTGTTA[C/T]TATCTGTAGAATATT | 51366 |
rs765202615 | in-del | -/T | 0.000137193 | 0.00828116 | intron-variant | UBR5 | GRCh38.p7 | 8:102299405 | ATCCAAAGTGTGTCC[-/T]TTTTTTCTTCCAGAT | 51366 |
rs765208864 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102374556 | TTACATAACTATTCC[C/T]TCAGCCTTAGAATAA | 51366 |
rs765215903 | snp | C/G | 1.65157e-05 | 0.0028736 | intron-variant | UBR5 | GRCh38.p7 | 8:102295561 | TGTTGTCGTGAGGAG[C/G]GAGGCTGAAAAGCTA | 51366 |
rs765226617 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102287073 | ACCCAGCTACTCAGG[C/G]GGCTGAGGTAGGAGC | 51366 |
rs765230914 | snp | A/C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102333304 | ATAAGTCATAGAAAA[A/C/T]AATGTTTTTATTGTT | 51366 |
rs765248165 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102352849 | CCTATCTAAAAACAC[C/T]CAAATTCTTTTCTAT | 51366 |
rs765261522 | snp | C/T | 1.64914e-05 | 0.00287149 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102279109 | GGATTTGGGGGTATA[C/T]ACCCAAGGAATGTCA | 51366 |
rs765264181 | snp | A/G | 0.000183993 | 0.00958971 | intron-variant | UBR5 | GRCh38.p7 | 8:102345386 | AATATATAAATAAAT[A/G]CAAAATTACCTCGAG | 51366 |
rs765304885 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102297138 | AGGGCTACAGCAAAT[-/A]ATACAGTTTATGATA | 51366 |
rs765305292 | snp | A/T | 3.29962e-05 | 0.00406165 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102259055 | GCAGCCATTTACCAA[A/T]AGCCTAAAATCTTCT | 51366 |
rs765310785 | snp | C/T | 1.72931e-05 | 0.00294045 | intron-variant | UBR5 | GRCh38.p7 | 8:102345582 | ACTGCAGCATACACA[C/T]AAAGAGCAACTGTAG | 51366 |
rs765314564 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102366559 | CTCTCCAGGTCTTCC[A/G]TCTCAAATTAAATAC | 51366 |
rs765316245 | snp | C/T | 1.64844e-05 | 0.00287087 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311487 | CATCTCGAAGAATAA[C/T]GGGAGATTCCTATAA | 51366 |
rs765323002 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102377574 | AGCCGGGCATTGTTG[A/G]ACGCGCCTATAGTCC | 51366 |
rs765349023 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102394654 | GCATTTGAACTGAAT[C/T]ATCCATTCAAGCTTG | 51366 |
rs765405251 | snp | A/C | 1.72865e-05 | 0.00293989 | intron-variant | UBR5 | GRCh38.p7 | 8:102261101 | CCACACATTAAGACA[A/C]AAATAGCCTCATTGG | 51366 |
rs765419033 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102396188 | AAAAAAAGCAGAAGA[A/G]CAGGTCTGAGGCAGG | 51366 |
rs765425720 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102409527 | TAATCTTACTACTTT[C/T]ATTCCAAAGTATAAA | 51366 |
rs765428209 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102340694 | TATGATAATGCTTAA[C/T]AGTTTAATTAAAGGC | 51366 |
rs765438927 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102292036 | ATGAGAGACATGGAA[A/G]TAAAGTAGAAACAGA | 51366 |
rs765443109 | snp | C/T | 1.6489e-05 | 0.00287128 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102346342 | ATCAAGATTTGTTCT[C/T]TGAAGTTCTCGAATA | 51366 |
rs765446221 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102339679 | TATGGACACTAACAA[C/T]CATACTTAATATTTA | 51366 |
rs765493483 | snp | C/G | 3.32912e-05 | 0.00407976 | intron-variant | UBR5 | GRCh38.p7 | 8:102326513 | TCTGAAGAGAAACGA[C/G]GTCCCTTAAGACAGG | 51366 |
rs765504755 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102353651 | ATCACCACTCATTAA[C/T]TGTAACACATGTACC | 51366 |
rs765510400 | in-del | -/AT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102390184 | TCATCTGAATAGTAC[-/AT]GTTTGCTCAAAATAA | 51366 |
rs765537888 | snp | A/C | 1.65647e-05 | 0.00287786 | intron-variant | UBR5 | GRCh38.p7 | 8:102360693 | AAAACAGAAAAAATT[A/C]TCCAAGTAAAAATGT | 51366 |
rs765543493 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102383469 | AATCAGTAATCAGCC[C/T]CCATCCCAGAATGCT | 51366 |
rs765552004 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102384373 | TATTTTAAAGGTTAG[C/T]ATACATTAACAGAAA | 51366 |
rs765553855 | in-del | -/TG | | | intron-variant | UBR5 | GRCh38.p7 | 8:102407745 | GAGACAAAGCAAAAC[-/TG]TGTCTCAAAAAAGAA | 51366 |
rs765560647 | in-del | -/TG | | | intron-variant | UBR5 | GRCh38.p7 | 8:102309039 | GATAGCTACACAATG[-/TG]TGTGTGTGTGTGTGT | 51366 |
rs765582993 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102293445 | CTTGATAATACAGTT[A/G]TTGTAGAAAAATATT | 51366 |
rs765597153 | in-del | -/ACA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102368114 | AATATAATTATTTTG[-/ACA]ACACACACAGAAAAA | 51366 |
rs765598313 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102391571 | TATTTATATACACAC[A/G]TATTTTGCAAATATA | 51366 |
rs765608839 | snp | C/T | 3.3173e-05 | 0.00407252 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285144 | TCTGCCTTCAAGTGT[C/T]CGTAAGCTAGCTTCT | 51366 |
rs765619340 | in-del | -/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102317464 | TGGAGCCCACCACAG[-/C]CTCAAGGAGGCCAGC | 51366 |
rs765620425 | in-del | -/TTCT | | | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102253238 | TATATAAACTTCCAG[-/TTCT]TTAAGTCAAAATTTT | 51366 |
rs765621971 | snp | C/G | 1.65433e-05 | 0.002876 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102298936 | CATTCGCCTTTCGAT[C/G]CTTGGATTCTACTAC | 51366 |
rs765628590 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102328845 | GACCTCATGATCCAC[C/G]CACCTCAGCCTCCCA | 51366 |
rs765641961 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102277756 | TCCTAGCACTCTGGG[A/T]GGCTGAAGTGGCTGG | 51366 |
rs765648450 | snp | C/T | 1.68803e-05 | 0.00290515 | intron-variant | UBR5 | GRCh38.p7 | 8:102265096 | AAGATTAAAGTTCTT[C/T]TACCTGCCAATGTTT | 51366 |
rs765656590 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102365382 | AGGCAGGAGAATCGC[A/T]TGAACCCGGGAGGCA | 51366 |
rs765692104 | snp | A/G | 1.65622e-05 | 0.00287764 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295040 | CAGTCCAGCCGAATT[A/G]TGCCACTTTGCTGAT | 51366 |
rs765694797 | snp | C/G | 1.6588e-05 | 0.00287988 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285235 | GGATGTCCAGGATCA[C/G]CAGCAGATGCTAATG | 51366 |
rs765699682 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102277692 | CCTTACCCACCCCCC[-/T]TCCTTTAAATTCACT | 51366 |
rs765704625 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102266437 | ACCTTCTATGTGCAA[C/T]TGTTTCAATGCCAAC | 51366 |
rs765711216 | snp | A/G | 6.59033e-05 | 0.00573997 | missense, nc-transcript-variant, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102276988 | TGAAAGATGTGAGAG[A/G]TGGCCCTTCACTTTC | 51366 |
rs765724322 | snp | C/T | 6.6036e-05 | 0.00574575 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102286571 | ATCACTTGAGTCATT[C/T]GATTGAGAATCATCT | 51366 |
rs765745162 | snp | A/G | 8.28768e-05 | 0.00643673 | intron-variant | UBR5 | GRCh38.p7 | 8:102295185 | ACATAAATCTAAAAA[A/G]GTTTTAATGAATACG | 51366 |
rs765748531 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102348533 | CCAAACATGAACATC[A/T]AGAAGATTAAATCAA | 51366 |
rs765751568 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102329970 | AAAAACGATGTCAAA[C/T]CAAAAGATTCTTTCC | 51366 |
rs765757137 | snp | C/T | | | synonymous-codon, nc-transcript-variant, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102277067 | ATCATGAGCAGATGG[C/T]CCTGGTTTTGAACTC | 51366 |
rs765761076 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102371871 | GGATTACAGGTGTGA[C/G]CCACTGCACCCAGCC | 51366 |
rs765769951 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102390812 | ATGAAGTTGCGAATC[C/T]TGCAAAAGGTACAAG | 51366 |
rs765791693 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102400300 | AAAAAAAAAGAAAGG[C/T]AGAAAAACAATACAT | 51366 |
rs765827041 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102356747 | CCTGGGTGACAGAGC[A/G]AGACTCCGTCTCAAA | 51366 |
rs765864509 | snp | C/T | 1.65154e-05 | 0.00287358 | intron-variant | UBR5 | GRCh38.p7 | 8:102275652 | GCATGACAGATTATT[C/T]CCTGAAATACATGCT | 51366 |
rs765889841 | snp | A/G | 1.6519e-05 | 0.00287388 | intron-variant | UBR5 | GRCh38.p7 | 8:102329218 | TTGAAAGCATAAAAA[A/G]AAATTACTATTTTAT | 51366 |
rs765893478 | snp | C/T | 3.34538e-05 | 0.00408971 | intron-variant | UBR5 | GRCh38.p7 | 8:102297639 | TAGCAGTTCATCTTT[C/T]AGGAAAGGACTTAAT | 51366 |
rs765904883 | snp | A/G | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102313811 | GAACAAACCTTGCCA[A/G]CAGGAACATTCTTGA | 51366 |
rs765914130 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102264627 | CCCCCACACATAATA[C/T]GTATTAATATTTTGA | 51366 |
rs765925050 | in-del | -/TTAG | | | intron-variant | UBR5 | GRCh38.p7 | 8:102335548 | AATTTATTTATTTAT[-/TTAG]TTAGTTAGTTTTTTG | 51366 |
rs765935191 | snp | A/G | 3.31912e-05 | 0.00407363 | intron-variant | UBR5 | GRCh38.p7 | 8:102293940 | TCTAAACCAAAATCA[A/G]AAAGGATGCCTTACT | 51366 |
rs765943123 | snp | A/T | 1.64898e-05 | 0.00287135 | intron-variant | UBR5 | GRCh38.p7 | 8:102329082 | AATCAATGCAAAGTG[A/T]TTCATACCTTGTTAT | 51366 |
rs765969816 | in-del | -/AT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102396623 | TATCTAAATTCAAAT[-/AT]ATATATATATACACA | 51366 |
rs765987896 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102338266 | AGTATCAACTTGGCT[G/T]GTTTCACTGTGAACA | 51366 |
rs765991683 | snp | A/G | 0.000104586 | 0.00723064 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102412267 | CCTCCACTCGAGGGC[A/G]GCCCCCTCCCGCTCT | 51366 |
rs765998212 | snp | C/T | 1.6617e-05 | 0.00288239 | intron-variant | UBR5 | GRCh38.p7 | 8:102312309 | CGGAGTCAGTTCCAA[C/T]ATTCACTTGCTGAAT | 51366 |
rs766011779 | snp | C/T | 1.64817e-05 | 0.00287064 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102312434 | GACAGTTAGTATTAC[C/T]GGAGGTTCCTGGAAA | 51366 |
rs766013942 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102348697 | TGACCTAGAGAGAGG[-/T]TATTTTACTCTCAGT | 51366 |
rs766020767 | snp | A/G | 1.64914e-05 | 0.00287149 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102279144 | GTCTGAACGTCGGAA[A/G]AATGGATGGTTTTGG | 51366 |
rs766021134 | snp | C/T | 4.95839e-05 | 0.0049789 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102294054 | ATAGCTTCTTCTCTA[C/T]GTCCAGGTGTATATT | 51366 |
rs766025861 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102345710 | TTAAAGAACATCAAA[C/T]GCATAAATGTCGCCT | 51366 |
rs766026062 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102358324 | TCATCTCTGCTGTTA[G/T]AGTACAAAGACAGCC | 51366 |
rs766026605 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102327457 | AAAAGATTTAAAATA[C/T]CCCAAATGTTAACTG | 51366 |
rs766067130 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102310522 | GGGCTAATTTTTGTA[C/T]TTTCAGTAGAGATAG | 51366 |
rs766087549 | in-del | -/GAG | 1.71029e-05 | 0.00292424 | intron-variant | UBR5 | GRCh38.p7 | 8:102311908 | CAGAAGCACATAAAT[-/GAG]AAGAAAAATTGTTAT | 51366 |
rs766108507 | snp | C/T | 1.65833e-05 | 0.00287948 | intron-variant | UBR5 | GRCh38.p7 | 8:102270207 | GAAGGAAAACTATTA[C/T]GACTTCATTTCCTTT | 51366 |
rs766116732 | in-del | -/AT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102295857 | GTTGACATTATGAAG[-/AT]GTATAACTCACTGAA | 51366 |
rs766117876 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102270248 | TAAAAATATTAGCAC[A/C]ACTAGTAAAAAAGTT | 51366 |
rs766130149 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102287418 | CAAGAAAGTAGTTGG[C/G]ATAAGGCAACATACC | 51366 |
rs766138148 | snp | C/T | 1.67357e-05 | 0.00289268 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102304015 | GTTTTTTCCTCCAAT[C/T]AAAGTTTCCTGGTAA | 51366 |
rs766156149 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102285097 | CCATTTTAAGTTGGG[G/T]ACGTTCTGTATATAT | 51366 |
rs766188711 | snp | C/G | 0.000500022 | 0.0158038 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102286399 | GGGCTGTACTGGCTG[C/G]TCGCTGATGCTGGGT | 51366 |
rs766250313 | in-del | -/T | 3.49205e-05 | 0.0041784 | intron-variant | UBR5 | GRCh38.p7 | 8:102298518 | AATTATATGTAAAAA[-/T]ATTAATTACTACTTA | 51366 |
rs766255094 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102289036 | TGGGTGTGGTGGTGC[A/G]CGCCTGTAATCCCAG | 51366 |
rs766257048 | snp | A/G | | | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102298463 | CCACTTACAGCTGAC[A/G]TAAATGGGGTCATCC | 51366 |
rs766261218 | snp | A/T | 1.65209e-05 | 0.00287405 | intron-variant | UBR5 | GRCh38.p7 | 8:102295572 | GGAGGGAGGCTGAAA[A/T]GCTACTCAGCTGTGC | 51366 |
rs766274172 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102408343 | AGAGGTTAAATGACT[A/G]GGCTACCAGCGCAGA | 51366 |
rs766308737 | snp | A/G | 1.71669e-05 | 0.00292971 | intron-variant | UBR5 | GRCh38.p7 | 8:102293567 | ACGACATTTCCAGAG[A/G]AGGATTAATCAGAAT | 51366 |
rs766309350 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102377729 | AAAAAAGGTAAAATA[A/C]CTACAGCCCAAATAA | 51366 |
rs766312595 | snp | A/T | 3.30846e-05 | 0.00406709 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295648 | TGCCTGCTGTTTGGC[A/T]GAGTAACCAGATTAG | 51366 |
rs766348514 | snp | C/T | 4.94222e-05 | 0.00497078 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102305195 | AATGTCTGCAGCATC[C/T]GTAGATTCTGCTCTA | 51366 |
rs766370177 | snp | C/G | | | upstream-variant-2KB, nc-transcript-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102412873 | GTTGTCGGGCCACGA[C/G]GCTGTAAGGCGCGTG | 51366 |
rs766370379 | snp | G/T | 1.69789e-05 | 0.00291362 | intron-variant | UBR5 | GRCh38.p7 | 8:102261299 | TTAAAGGCAATTTTG[G/T]CAAAGCAGTAAAACA | 51366 |
rs766377275 | snp | A/G | 8.05121e-05 | 0.00634425 | intron-variant | UBR5 | GRCh38.p7 | 8:102271287 | ATTTAGATGAATGCA[A/G]ATTCAACTACCTTAA | 51366 |
rs766397558 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102367820 | AACCACAATCTCACA[A/C]AAATATATACACTCC | 51366 |
rs766398664 | snp | A/C | 1.66346e-05 | 0.00288393 | synonymous-codon, nc-transcript-variant, intron-variant | UBR5 | GRCh38.p7 | 8:102285276 | ACGTAATTGAGCTTC[A/C]GTAGAATCCATAATA | 51366 |
rs766418254 | snp | A/G | 1.65504e-05 | 0.00287662 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285150 | TTCAAGTGTTCGTAA[A/G]CTAGCTTCTTCTCGC | 51366 |
rs766432894 | in-del | -/AAT | | | intron-variant, downstream-variant-500B, nc-transcript-variant | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102252022 | CCTTTAAAATGTAAA[-/AAT]AATAGTATCTTTATG | 51366 |
rs766437018 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102267310 | TCAGAGGGAGCACTA[C/T]AGAAGAACAGAAAAA | 51366 |
rs766458378 | snp | C/T | 3.36922e-05 | 0.00410426 | intron-variant | UBR5 | GRCh38.p7 | 8:102298840 | AAAAATATATCAAAT[C/T]CTCTTACTTGGCAGA | 51366 |
rs766480303 | snp | A/C | 4.97063e-05 | 0.00498505 | intron-variant | UBR5 | GRCh38.p7 | 8:102326532 | CCTTAAGACAGGCTA[A/C]ATCCATCACTTACCT | 51366 |
rs766480941 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102375101 | CACGGTGGCTCACAC[A/C]TGCAATCCCAGCACT | 51366 |
rs766509015 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102259546 | ACTGAGAAATTATGA[C/T]GTGCCAGGAATTGTC | 51366 |
rs766511168 | in-del | -/ACA | 6.62685e-05 | 0.00575585 | intron-variant | UBR5 | GRCh38.p7 | 8:102360235 | AGACCAACATTTTTT[-/ACA]ACCCTGTTATTTCAA | 51366 |
rs766513098 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102272349 | ATCAAAATAAATGTG[A/T]CCGTAGAATAGCAAA | 51366 |
rs766523293 | in-del | -/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102398606 | GCCAACATGGTCAAA[-/C]CCTGTCTCTACTAAA | 51366 |
rs766523942 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102280138 | GGTAAACATAATACT[A/G]AGACAAATACAAGAA | 51366 |
rs766537470 | in-del | -/ATA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102331191 | AGTGAACAGGAGGCT[-/ATA]ATAAGTTTTGGGGGA | 51366 |
rs766580965 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102330110 | AAGCTTGGCTAATAA[A/C]TGTAAATAAATAATT | 51366 |
rs766587123 | snp | A/C | 3.31521e-05 | 0.00407123 | intron-variant | UBR5 | GRCh38.p7 | 8:102360698 | AGAAAAAATTATCCA[A/C]GTAAAAATGTGTATT | 51366 |
rs766595940 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102361265 | AAATACATCATAGGG[C/T]TTACTCTTAAATACA | 51366 |
rs766601131 | snp | A/T | 3.30469e-05 | 0.00406477 | intron-variant | UBR5 | GRCh38.p7 | 8:102329065 | TTAAAGCATGAAATG[A/T]TAATCAATGCAAAGT | 51366 |
rs766607803 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102362301 | AAACAGTCTTGAATG[C/T]AAAACACTATAATAG | 51366 |
rs766617189 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102306296 | TAGAAAAAAGCAGGT[G/T]GGAAAAGAGCATGTG | 51366 |
rs766625906 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102325769 | ATATAAACAATTTTT[-/A]TGGAAAATAGATTTT | 51366 |
rs766626611 | snp | A/G | 1.65463e-05 | 0.00287626 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102298947 | CGATCCTTGGATTCT[A/G]CTACAGATGGCTCTG | 51366 |
rs766633814 | snp | C/T | 1.67961e-05 | 0.00289789 | intron-variant | UBR5 | GRCh38.p7 | 8:102329435 | CTATAAATATAAAAA[C/T]TGCCAAATCTACTGA | 51366 |
rs766636813 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102342023 | TCAAAGAACACAGAT[C/G]CCTAATCTTGTCATG | 51366 |
rs766640083 | snp | A/G | 1.65318e-05 | 0.002875 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102361177 | CACTGTTTAATAGTA[A/G]CCTGTTCCAATACAT | 51366 |
rs766640515 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102391653 | AAGTTACAGAAGATA[C/T]ATCCTCCTCCATCTA | 51366 |
rs766653944 | snp | C/T | 3.37012e-05 | 0.00410481 | intron-variant | UBR5 | GRCh38.p7 | 8:102294968 | TACTTGTAATACACA[C/T]TCAAAGAACTTACCA | 51366 |
rs766654722 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102281659 | TTTAGAAATATAACC[A/G]CTGTGCATGATTTAC | 51366 |
rs766658101 | snp | C/G | 1.71613e-05 | 0.00292923 | intron-variant | UBR5 | GRCh38.p7 | 8:102311910 | GAAGCACATAAATGA[C/G]AAGAAAAATTGTTAT | 51366 |
rs766669672 | snp | A/C | 1.67556e-05 | 0.0028944 | intron-variant | UBR5 | GRCh38.p7 | 8:102285474 | AATTGACAGCCAAAA[A/C]AAAATAGTGGAATGG | 51366 |
rs766683828 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102374226 | TTGGATAGCTCACTA[C/T]ATTGCTACTTCAACT | 51366 |
rs766719436 | in-del | -/TA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102305542 | ATATTTTTAGCTTTC[-/TA]TCAACTAACTCAGCT | 51366 |
rs766720755 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102343870 | AAAAAAAGGGGGGGG[G/T]GGGCAGGGGGGAGAA | 51366 |
rs766734664 | snp | A/G | 8.38567e-05 | 0.00647467 | intron-variant | UBR5 | GRCh38.p7 | 8:102313964 | AGAAAATGTAAAAGA[A/G]ACTTTATAGATTTCA | 51366 |
rs766741930 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102293507 | TTACACAAATGATCA[G/T]GTACACCACCTGAGT | 51366 |
rs766749244 | snp | A/G | 3.31603e-05 | 0.00407174 | intron-variant | UBR5 | GRCh38.p7 | 8:102295200 | GGTTTTAATGAATAC[A/G]TACGGGTCTTTATTC | 51366 |
rs766755885 | snp | A/C | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102277023 | AGTCCTATTTCTGCT[A/C]GTAAGCTACTTTTTA | 51366 |
rs766757280 | snp | G/T | 1.87499e-05 | 0.0030618 | intron-variant | UBR5 | GRCh38.p7 | 8:102257583 | ATCATACATGGTATT[G/T]TTAACTTCTGTATTT | 51366 |
rs766758618 | snp | A/G | 1.64792e-05 | 0.00287042 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102342526 | CTGGACTTTGAACAG[A/G]TGTATTCTTCTTATC | 51366 |
rs766760913 | snp | A/G | 3.31719e-05 | 0.00407245 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295321 | AAATCATGATCTGGC[A/G]TATCTGAATCTAAAA | 51366 |
rs766767834 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102266533 | TTCTTTGAAGAATGA[C/G]TCCCAGGAGTCCTAG | 51366 |
rs766794225 | snp | C/G | 3.29489e-05 | 0.00405874 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102313822 | GCCAACAGGAACATT[C/G]TTGACATCTTCCACA | 51366 |
rs766821168 | in-del | -/A | 1.67514e-05 | 0.00289403 | intron-variant | UBR5 | GRCh38.p7 | 8:102261265 | TGAGTTCAACCTGTG[-/A]AAAATTTACCAGTGC | 51366 |
rs766823258 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102300464 | ACAGTTCAGATAAAA[C/G]AACAGCTAAACATTA | 51366 |
rs766834189 | snp | C/T | | | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102346941 | TGACAGATGCTGGAA[C/T]AACTGGCTGGGGCTG | 51366 |
rs766842079 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102379703 | AACACTTCTTAACAA[C/G]TATTTACTGAATATT | 51366 |
rs766845124 | snp | C/T | 1.64961e-05 | 0.00287189 | intron-variant | UBR5 | GRCh38.p7 | 8:102266898 | TTATTGAAATTTCCT[C/T]GTAATTTAAATTCTG | 51366 |
rs766845198 | snp | A/G | 1.64852e-05 | 0.00287094 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102277146 | CGGTTTTGCATGTTC[A/G]TTACATTTTTCAGAT | 51366 |
rs766857155 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102403046 | ACAAAAATTTGCTGT[C/G]AAGAAAAATCTAGGT | 51366 |
rs766895757 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102312962 | TTAACAAATTTAAAC[A/G]GCCACATATACAGCT | 51366 |
rs766923958 | snp | A/G | 3.33172e-05 | 0.00408136 | intron-variant | UBR5 | GRCh38.p7 | 8:102281272 | TCTTAAATCAACCTC[A/G]TGGCAAGAATGGATA | 51366 |
rs766926232 | snp | G/T | 1.65701e-05 | 0.00287833 | intron-variant | UBR5 | GRCh38.p7 | 8:102288131 | TTTACTCATACTGAG[G/T]AATTTCTCAAATAAC | 51366 |
rs766976023 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102336926 | TCTGTACATTACTTT[A/G]AGCAGTATAAGTTTA | 51366 |
rs766976296 | snp | C/T | 1.71366e-05 | 0.00292712 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102314827 | GGACCCATTTCTGTT[C/T]TCACTGGCTCCTGCT | 51366 |
rs766993335 | in-del | -/TA | 1.827e-05 | 0.00302236 | intron-variant | UBR5 | GRCh38.p7 | 8:102298348 | GGACAGAAGAGAATC[-/TA]TCCAAACTGAATGTA | 51366 |
rs766997700 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102279649 | CTGAAACCTGAGCAT[G/T]TGCTAAGCAGAGTAA | 51366 |
rs767003917 | snp | A/T | 1.70621e-05 | 0.00292074 | intron-variant | UBR5 | GRCh38.p7 | 8:102265087 | TTCAAACCCAAGATT[A/T]AAGTTCTTTTACCTG | 51366 |
rs767022202 | snp | C/T | 1.67086e-05 | 0.00289033 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102265268 | GAGCCATGGCGCTTT[C/T]GGTTTTCCTGCTAAC | 51366 |
rs767048268 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102366903 | CCATGTTGGAGAAAG[C/T]AGGTATTGCCAAAAC | 51366 |
rs767048940 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102397431 | GGTGCGGTGGCTCAC[A/G]CCCGTAATCCCAGTA | 51366 |
rs767059462 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102404363 | TTTTGTTACCACTAC[A/T]CTGATTGTCTCAAGA | 51366 |
rs767084751 | snp | C/T | 1.64822e-05 | 0.00287068 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102286545 | TCACTCTGACTACTA[C/T]TGCTATCAGAATCAC | 51366 |
rs767087010 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102316856 | CCTGCAAAGGATACA[A/G]TCTAATAACAAAACG | 51366 |
rs767112828 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102340919 | CACTAAAAGTCTATA[C/T]AGTGCCAAGATTTCA | 51366 |
rs767123339 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102264823 | AGGTCATCCTCCTAC[A/G]CCAGCCTCCCAAGTA | 51366 |
rs767129530 | in-del | -/T | 1.65023e-05 | 0.00287244 | intron-variant | UBR5 | GRCh38.p7 | 8:102288284 | AAATCCAGAATCTTA[-/T]TTGTAGACAATCAAA | 51366 |
rs767142417 | snp | C/T | 3.34767e-05 | 0.00409112 | intron-variant | UBR5 | GRCh38.p7 | 8:102305039 | TTACATTTTCAAAAT[C/T]GCCTAAAACTCCCTT | 51366 |
rs767143872 | snp | A/G | 1.65222e-05 | 0.00287417 | missense, upstream-variant-2KB, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102304068 | TTGATGATCCAGCCC[A/G]ATTACCTGGGCCATT | 51366 |
rs767163403 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102334458 | TACCGCACCTGGCTA[A/G]TTTTTGTATTTTTAG | 51366 |
rs767167814 | snp | A/T | 1.64846e-05 | 0.0028709 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102312453 | GGTTCCTGGAAATTT[A/T]ACAGCAACATAGGCA | 51366 |
rs767168146 | snp | A/T | 1.66538e-05 | 0.00288559 | intron-variant | UBR5 | GRCh38.p7 | 8:102329408 | TTCCATCCTATAAAG[A/T]AAAATACAATACTAT | 51366 |
rs767186381 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102310917 | CATATCAAAAAAAAG[G/T]ACTTTCTCCCAACTT | 51366 |
rs767195655 | snp | C/G | 1.65436e-05 | 0.00287602 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295663 | AGAGTAACCAGATTA[C/G]TAGCAGTGAGCAGGC | 51366 |
rs767206412 | snp | C/T | 3.51692e-05 | 0.00419325 | intron-variant | UBR5 | GRCh38.p7 | 8:102346855 | CATATTCAGTAAAAC[C/T]TCACCTTGTCCTGTT | 51366 |
rs767221292 | snp | G/T | 6.59805e-05 | 0.00574333 | intron-variant | UBR5 | GRCh38.p7 | 8:102313790 | TAATTAAGTTTTAGA[G/T]ATCTTGAACAAACCT | 51366 |
rs767226841 | in-del | -/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102380094 | CCATCTAACAGAAGA[-/G]GAAAAAAACAGCAAA | 51366 |
rs767234187 | snp | C/T | 1.70915e-05 | 0.00292326 | intron-variant | UBR5 | GRCh38.p7 | 8:102261128 | TTGGATCACACAACA[C/T]TTTCTAGAAACACTT | 51366 |
rs767234462 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102369535 | TCTAAAATTTGCTTG[-/A]AAAGTTCAAATTTAT | 51366 |
rs767291606 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102307227 | TTGGGATGTAGATTA[C/T]GAGGCCCAATTTCAC | 51366 |
rs767310871 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102298751 | ATTGTTTTAAATTTA[C/T]ATAACTATTGTCCAT | 51366 |
rs767322645 | snp | C/T | 4.94393e-05 | 0.00497164 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102346971 | GACTGCCCAAAAGCC[C/T]AGACCCTCGATCCCG | 51366 |
rs767325418 | snp | G/T | 3.35948e-05 | 0.00409833 | intron-variant | UBR5 | GRCh38.p7 | 8:102280358 | ACTGAGGCAGCCATT[G/T]CTTGAAGTAGATTAG | 51366 |
rs767346062 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102408447 | AATCCTTTTGATATG[A/G]CAATCTCAATAAAGA | 51366 |
rs767353272 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102267493 | GCAACTCTTAACATA[C/T]ACTCACAAAAATCTT | 51366 |
rs767372964 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102379404 | AGAAAACAAACCTAA[C/T]AAAATGGAGGCAGTC | 51366 |
rs767403107 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102409431 | GTAAAGAAAGAAAAC[A/G]TATTTGAAGAAAACA | 51366 |
rs767408837 | snp | C/G | 1.70781e-05 | 0.00292212 | intron-variant | UBR5 | GRCh38.p7 | 8:102293579 | GAGAAGGATTAATCA[C/G]AATCTGTTACCTGGT | 51366 |
rs767422054 | snp | C/G | 6.72224e-05 | 0.00579713 | intron-variant | UBR5 | GRCh38.p7 | 8:102326678 | CCTGAAAACAAAAAA[C/G]ATAAATTGGTCAAAT | 51366 |
rs767442642 | in-del | -/GC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102317244 | TCCCACCTGAATACT[-/GC]GCTTTTCTGACGGGC | 51366 |
rs767450661 | snp | C/G | 1.64806e-05 | 0.00287054 | intron-variant | UBR5 | GRCh38.p7 | 8:102296850 | CAATATAAATCTAAA[C/G]AGCTTATAATATTAA | 51366 |
rs767452731 | snp | A/G | 1.71305e-05 | 0.00292659 | intron-variant | UBR5 | GRCh38.p7 | 8:102261307 | AATTTTGTCAAAGCA[A/G]TAAAACATTACTGTT | 51366 |
rs767465213 | snp | A/C | 6.65657e-05 | 0.00576875 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102312182 | TTTTTTCAGGTATAC[A/C]AAGCTTTTTAGGAGT | 51366 |
rs767514223 | snp | G/T | 1.64958e-05 | 0.00287187 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102277164 | ACATTTTTCAGATTG[G/T]CAGCATAAGACATTT | 51366 |
rs767516461 | snp | C/T | 1.6557e-05 | 0.00287719 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102361188 | AGTAGCCTGTTCCAA[C/T]ACATTCAAAGGGGGG | 51366 |
rs767516890 | snp | A/C | 1.6676e-05 | 0.00288751 | intron-variant | UBR5 | GRCh38.p7 | 8:102285500 | AATGGGAAACTTTTC[A/C]GTGGTTTCATACCTG | 51366 |
rs767529440 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102375378 | AAAAATAAAAATAAA[A/G]TGAATAAAAAATAAA | 51366 |
rs767537741 | snp | A/T | | | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102413014 | GCCGGGAGGGAGGGT[A/T]AGTGTGTGTCCCAGA | 51366 |
rs767540148 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102342244 | TTTACTTTATCAAGT[A/C]GTAAGATACGTTGCA | 51366 |
rs767544760 | in-del | -/TA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102397255 | TTCTTCCCTATCACT[-/TA]TATATCAATTAGCAC | 51366 |
rs767550615 | snp | G/T | 3.47313e-05 | 0.00416706 | intron-variant | UBR5 | GRCh38.p7 | 8:102311921 | ATGAGAAGAAAAATT[G/T]TTATACATCTTATCT | 51366 |
rs767554596 | in-del | -/TCA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102392087 | CCTTCCCAGAAAAAC[-/TCA]TCATGAATAATCCCT | 51366 |
rs767612188 | in-del | -/A | 0.000144617 | 0.0085022 | intron-variant | UBR5 | GRCh38.p7 | 8:102323544 | CATAACTTTAAAAAT[-/A]TATATAATATTTATT | 51366 |
rs767619171 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102386094 | TTCATAAATAGGTAA[C/T]GGCATACTGGCTTCA | 51366 |
rs767658152 | snp | C/T | 1.64792e-05 | 0.00287042 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102342534 | TGAACAGGTGTATTC[C/T]TCTTATCCAAGTTTG | 51366 |
rs767661270 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102368880 | GTTTGATTCTCAAAC[C/T]TGTTAAATCTCAAGA | 51366 |
rs767664572 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102281901 | TTGATGGTGTTGTTC[C/T]AGGGACCATACTTTG | 51366 |
rs767667922 | snp | C/G | 1.64787e-05 | 0.00287038 | intron-variant | UBR5 | GRCh38.p7 | 8:102268932 | ACATACTGAAAGTAA[C/G]TAGCTGATGTTTAAA | 51366 |
rs767676724 | snp | C/T | 1.656e-05 | 0.00287745 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102298955 | GGATTCTACTACAGA[C/T]GGCTCTGTGGAAGGA | 51366 |
rs767706841 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102364144 | TCTTTTAGTCATCTC[C/T]GGTTCTGAAAATTCT | 51366 |
rs767708650 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102380823 | GTAGCTGGGACTACA[C/G]GCAAGCACCAACATG | 51366 |
rs767769125 | in-del | -/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102406288 | GGTTTTTTATTGTTT[-/G]TTTTTGGTTTTGTTT | 51366 |
rs767782824 | snp | C/G | 0.000378559 | 0.0137527 | intron-variant | UBR5 | GRCh38.p7 | 8:102314705 | CAGCTGTCTGCATGA[C/G]ACCTATTTTCACAAA | 51366 |
rs767790976 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102347276 | TAATACTGTTTTTTA[A/C]AGAAATGGGGTCTTG | 51366 |
rs767794039 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102331748 | GCCTCTGTTCATTAT[C/G]TGTTCTGGAACCCAT | 51366 |
rs767796952 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102376653 | GGATTACAGGCGCCC[A/G]CTACCACACCTGGCT | 51366 |
rs767797278 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102282231 | TTACGAAAATTAAAA[C/T]TGTACTTTCAAGGAT | 51366 |
rs767802584 | snp | A/C | 1.64765e-05 | 0.00287019 | stop-gained, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102288236 | CATCATGATGATCCT[A/C]TTCTCCAGCCACACC | 51366 |
rs767803410 | snp | C/G/T | 3.32935e-05 | 0.00407993 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102299502 | CCGGTTGCTGCTGTG[C/G/T]TAAGAGATCCCACAG | 51366 |
rs767807709 | in-del | -/A | 2.62037e-05 | 0.00361956 | intron-variant | UBR5 | GRCh38.p7 | 8:102257763 | ATACCAGTTGTTGTT[-/A]ATTATCTGTAGAATA | 51366 |
rs767818506 | snp | A/C | 6.61059e-05 | 0.00574879 | intron-variant | UBR5 | GRCh38.p7 | 8:102278810 | TTATATTGCAAAAAA[A/C]CTTTTACTGTCTTAC | 51366 |
rs767824107 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102267572 | TATACCAGTATGCAG[C/T]AGCTCCAGAGACAGG | 51366 |
rs767849366 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102362439 | ACTGCCTGATCTGAT[A/C]TTTTAAAACCGTTTT | 51366 |
rs767856265 | snp | C/T | 4.94499e-05 | 0.00497217 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311340 | CTTTCTTTTTGATTG[C/T]TGAATTGGCAGGAAG | 51366 |
rs767891078 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102407172 | TGGAGTGCAGTGGCG[C/T]GATCTTGGCTCACTG | 51366 |
rs767900132 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102404713 | GGGAGTTCGAGACCA[C/G]CCTGACCAACATGGT | 51366 |
rs767901652 | snp | C/T | 2.58288e-05 | 0.00359357 | intron-variant | UBR5 | GRCh38.p7 | 8:102314875 | TAAGAAATAAGATTC[C/T]CCTTATAATTAGATA | 51366 |
rs767914883 | snp | C/T | 3.39443e-05 | 0.00411959 | intron-variant | UBR5 | GRCh38.p7 | 8:102269157 | CTCTAAAACCTCTTG[C/T]CTAATTACATCTACA | 51366 |
rs767915089 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102259212 | AGACATAATTTTAGC[A/G]GCCTTCTCTAACAAT | 51366 |
rs767921986 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102302107 | GAGGGGGCCATTCCT[C/T]GTCATTTTTAAAATT | 51366 |
rs767927108 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102404808 | GCCACTTGGGAAGCT[A/G]AGGCAGGAGAATCAC | 51366 |
rs767932912 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102393492 | ATACAAAAAATTAGC[A/C]ACGCATGGTAGCACA | 51366 |
rs767956713 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102289956 | TAAGAGATCTGACAT[A/G]ATTTCTATTTTGAAT | 51366 |
rs767979073 | snp | A/G | 0.000198426 | 0.00995859 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102297506 | ACTGCAAGTGTCATT[A/G]CAACATAAAACATAT | 51366 |
rs767984006 | snp | A/T | 1.7865e-05 | 0.00298867 | intron-variant | UBR5 | GRCh38.p7 | 8:102257613 | TCCTTCTACAAATCT[A/T]GTGAAATTTTTAACT | 51366 |
rs767989102 | in-del | -/AG | | | intron-variant | UBR5 | GRCh38.p7 | 8:102409754 | GTCTCTTTTGGAAAC[-/AG]ATTTTTCTCAAGTGA | 51366 |
rs767994308 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102257750 | AAATAAAATATACTA[C/T]ACCAGTTGTTGTTAT | 51366 |
rs768003615 | in-del | -/AAAAAAAC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102392616 | AGATACCAAAAAAAA[-/AAAAAAAC]AAAAAACAAAAAACA | 51366 |
rs768017496 | snp | C/T | 1.648e-05 | 0.0028705 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102342608 | GGCTCCATCAAGCCA[C/T]CTTCGTTCACGTAAA | 51366 |
rs768017705 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102301602 | ACTCCTTACCAGTAA[C/T]AGCACACACCATGGT | 51366 |
rs768022941 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102392761 | AATTTAATATAGATA[C/T]ATGCTAATGTACCTC | 51366 |
rs768028682 | in-del | -/AA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102378661 | AAAAAGGAGGAAAAA[-/AA]AAAAAAAAAAAAAAT | 51366 |
rs768041609 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102370818 | TGGGATCATATATGG[C/G]ATGATATATGGGATC | 51366 |
rs768054754 | snp | G/T | 9.88452e-05 | 0.00702942 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102269040 | CAGAGAATCCTCACT[G/T]GCTAGAAGGAGAAGC | 51366 |
rs768056062 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102339000 | TGGCACATATTTAAT[A/C]AAGGTTTCTAAAGTA | 51366 |
rs768061013 | snp | A/G | 1.8258e-05 | 0.00302137 | intron-variant | UBR5 | GRCh38.p7 | 8:102275497 | TACTACAGGTATAGT[A/G]TAAGAAAATCTAAAT | 51366 |
rs768083420 | snp | A/C | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311466 | TTGGGTAGATGGTAC[A/C]ATTTCCATCTCGAAG | 51366 |
rs768093953 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102268158 | CTGCAAGCTCCACCC[G/T]CCTGGGTTCAAGCTA | 51366 |
rs768095699 | in-del | -/ACAATCTA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102369161 | CTGCCTTTATCTATC[-/ACAATCTA]ACAATATATTGTTTT | 51366 |
rs768143368 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102337875 | GAAATTTCTAATCTA[C/G]AAAAAATAAATTGCA | 51366 |
rs768146440 | snp | G/T | 5.77017e-05 | 0.00537099 | intron-variant | UBR5 | GRCh38.p7 | 8:102257729 | TCTCCTAAGAATGAA[G/T]AATGTAAATAAAATA | 51366 |
rs768147106 | snp | C/T | 1.66103e-05 | 0.00288182 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295302 | GGCAAATCTTGGAGG[C/T]TCTAAATCATGATCT | 51366 |
rs768156387 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102405680 | AAAAATTAGCCAGGT[A/G]TGGTGGCGTGCGCCT | 51366 |
rs768175901 | in-del | -/CCT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102264657 | AGAAATTCTCTACAG[-/CCT]CCTTTCTATTCAGCA | 51366 |
rs768179706 | snp | C/T | 3.32287e-05 | 0.00407593 | intron-variant | UBR5 | GRCh38.p7 | 8:102288109 | ATCTCCCTTTAAAAG[C/T]ACCTGATTTACTCAT | 51366 |
rs768183782 | in-del | -/ACAAA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102372375 | ACAAAACACAGAAAG[-/ACAAA]ACAAAAGATGGTTTT | 51366 |
rs768187714 | in-del | -/AAATG | | | intron-variant | UBR5 | GRCh38.p7 | 8:102283367 | GGGGTGAGTAGGGGA[-/AAATG]AAATGAAGAATGACT | 51366 |
rs768188553 | snp | A/C | 1.64808e-05 | 0.00287057 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102360165 | TTGACGTCCTCCCTG[A/C]CCCCGAGTTGCTGTT | 51366 |
rs768196086 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102257598 | TTTAACTTCTGTATT[G/T]CCTTCTACAAATCTT | 51366 |
rs768198984 | snp | C/T | 1.64895e-05 | 0.00287132 | intron-variant | UBR5 | GRCh38.p7 | 8:102267038 | CTTTCACATTCCAGA[C/T]AACGGAGACTTCTAG | 51366 |
rs768200205 | snp | C/G/T | 3.29855e-05 | 0.00406102 | intron-variant | UBR5 | GRCh38.p7 | 8:102295394 | TTCCCACAAGTGTCA[C/G/T]AAATGTCTAATTAAC | 51366 |
rs768209011 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102387361 | GTCCATTAGGTTTTT[A/T]AAATATCTCTAATGT | 51366 |
rs768210621 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102360731 | AATTTGAATTTATTC[A/G]ACAAAGAGATTCTGT | 51366 |
rs768212554 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102332414 | AAGTCACTTCTCTAC[A/G]GACTCTGTTGACTTC | 51366 |
rs768243737 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102363459 | TGAGCTCTAAGAGAA[A/G]GCTGACTAGAAAATA | 51366 |
rs768265698 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102381844 | ATTTAAAAAAGTCAA[A/G]AAAGAAAAAAGGCAA | 51366 |
rs768324880 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102269270 | CTGGAAGATCAATTA[C/T]AGAGAAACTTGGCAG | 51366 |
rs768326292 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102323605 | ACTGGGCTTCCTAGG[-/T]TTCCCAGTATAATCT | 51366 |
rs768346858 | snp | C/G | 1.73857e-05 | 0.00294831 | intron-variant | UBR5 | GRCh38.p7 | 8:102285091 | GAGGATCCATTTTAA[C/G]TTGGGGACGTTCTGT | 51366 |
rs768356367 | snp | C/T | 1.71696e-05 | 0.00292993 | intron-variant | UBR5 | GRCh38.p7 | 8:102323301 | CGATTAGTTAAGCTA[C/T]AGTACTTACTTAGCT | 51366 |
rs768421601 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102352222 | ACTGAGGCAGGAGAA[C/T]CACTTGAACCCAGGA | 51366 |
rs768424230 | snp | C/G | 8.25484e-05 | 0.00642397 | intron-variant | UBR5 | GRCh38.p7 | 8:102360205 | CCTGGGGGAAAGCAA[C/G]AGGTAAATTTTTGAA | 51366 |
rs768427401 | snp | C/T | 1.66217e-05 | 0.0028828 | intron-variant | UBR5 | GRCh38.p7 | 8:102311275 | GTGAATTAAAATGCC[C/T]AGTAGTTTCAATACT | 51366 |
rs768429375 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102325022 | GTAATGCCATATTAC[A/C]TGCTGATATGGCAGC | 51366 |
rs768436793 | snp | A/G | 3.30792e-05 | 0.00406675 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102275792 | TCCTAGCAGCATATC[A/G]TGGGAAATAACCATT | 51366 |
rs768439938 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102351277 | CAATTGCCAAGTGGT[A/G]GAAGCTACCCAAATG | 51366 |
rs768441593 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102364541 | ATGGAAGATATATAC[A/G]TAATGTTTACAATGA | 51366 |
rs768479695 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102356605 | TCTACTAAAAATACA[A/G]AAAAATTACCTGGGC | 51366 |
rs768487423 | snp | C/T | 1.65059e-05 | 0.00287275 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102281483 | GTCTCCTCGTGCAGA[C/T]ATCATTCCTTGACGG | 51366 |
rs768499986 | in-del | -/ATTC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102274829 | GGAGTATCAATATTA[-/ATTC]ATTATTTGATTTTTT | 51366 |
rs768503718 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102275622 | ATTCAGTTAGGATCT[C/T]AAAAAAAAAAAAATG | 51366 |
rs768519325 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102309280 | GGCTGGCCTCAAACT[C/T]CTGGCCTCAAGGGAT | 51366 |
rs768525879 | snp | A/T | 8.12463e-05 | 0.00637311 | intron-variant | UBR5 | GRCh38.p7 | 8:102327933 | CTTTAAATAAAATCA[A/T]GCCATCTTTTCAAAA | 51366 |
rs768526810 | snp | C/T | 1.65127e-05 | 0.00287334 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102294031 | GTAGAAACCTCATTG[C/T]CACAGCAATAGCTTC | 51366 |
rs768542161 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102362225 | AAAAACCCCAAAGGG[A/C]TACATAACAAAGAGA | 51366 |
rs768559990 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102296308 | TAATGGTACGGTAGA[C/T]GGTTTTTACAGTCCA | 51366 |
rs768562081 | snp | A/C | | | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102413819 | ACTATAAGACACTTT[A/C]AGAGTTTTGGCCACG | 51366 |
rs768610961 | snp | A/T | 1.66054e-05 | 0.00288139 | intron-variant | UBR5 | GRCh38.p7 | 8:102297616 | TTTCAGCTAAAAAAG[A/T]AAGAACATAGCAGTT | 51366 |
rs768612887 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102298152 | ACACTGTTCATTACG[A/G]AGTGTTTATTCTTAA | 51366 |
rs768614521 | in-del | -/TC | 1.83883e-05 | 0.00303213 | intron-variant | UBR5 | GRCh38.p7 | 8:102257602 | ACTTCTGTATTTCCT[-/TC]TACAAATCTTGTGAA | 51366 |
rs768618410 | snp | A/G | 1.73294e-05 | 0.00294353 | intron-variant | UBR5 | GRCh38.p7 | 8:102286352 | CAATACTAAGTTTTC[A/G]GACTTGCCTGCTGGT | 51366 |
rs768642385 | snp | C/G | 3.29527e-05 | 0.00405898 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102329163 | TTTTCATTGGTTAAC[C/G]CCAAAAATGTTGCTC | 51366 |
rs768666070 | snp | A/C/G | 0.000115242 | 0.00759012 | intron-variant | UBR5 | GRCh38.p7 | 8:102264424 | TGATTATTTTATAAA[A/C/G]GAAAATTTTTGCAAT | 51366 |
rs768680319 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102276473 | ATTAGTAATAACAAA[C/T]AGCTTTTTAGCTGGC | 51366 |
rs768697447 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102298204 | GTTTTTTGATGGAAA[A/G]TTGGAAGATACAGTA | 51366 |
rs768717988 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102339952 | TGGTATGTCAAGAAC[A/G]TAGAAATAACACTTT | 51366 |
rs768718218 | in-del | -/AAAAA | | | utr-variant-3-prime, downstream-variant-500B | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102252324 | TTTTATGATTTACTT[-/AAAAA]AAAAATCTTTTACTA | 51366 |
rs768732984 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102284893 | AACAAAAAATTAGCC[A/G]GGCGTGGGTGGCAAG | 51366 |
rs768736267 | snp | C/G | 1.65179e-05 | 0.00287379 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102279042 | TTAATTCACCTGCAA[C/G]AGATGTGGCTGATCA | 51366 |
rs768756003 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102399579 | ATTATGCCCAGCCTA[C/T]ATCTCATCAATTTAC | 51366 |
rs768757084 | snp | A/T | 1.64917e-05 | 0.00287151 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102312389 | CCTGCAGGAGAGAAG[A/T]AGGGTCAGCATCTGG | 51366 |
rs768773749 | snp | A/G | 5.04096e-05 | 0.00502018 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102304177 | CTCCGCTTCTGAAAA[A/G]TGAGAAAAAATTAAG | 51366 |
rs768779781 | snp | A/G | 7.45365e-05 | 0.00610432 | intron-variant | UBR5 | GRCh38.p7 | 8:102294123 | TCTAAAAGCTTTAAA[A/G]AATTATATTCACTCT | 51366 |
rs768786273 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102347708 | CAGTAGCACGATCTC[A/G]GCTCACTGCAACCTC | 51366 |
rs768787498 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102297638 | ATAGCAGTTCATCTT[C/T]CAGGAAAGGACTTAA | 51366 |
rs768812611 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102407171 | CTGGAGTGCAGTGGC[A/G]CGATCTTGGCTCACT | 51366 |
rs768814975 | snp | A/G | 3.29968e-05 | 0.00406169 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102346255 | AGGCAAATAAGATTC[A/G]CTGGCTGTATCATCC | 51366 |
rs768822067 | snp | C/T | 5.01115e-05 | 0.00500532 | intron-variant | UBR5 | GRCh38.p7 | 8:102312515 | AAATTCAATGAACAT[C/T]AGCAATAGCTTATAT | 51366 |
rs768836632 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102264278 | CCCCATAGTCTTTTT[C/T]TGTCATTAATTTATT | 51366 |
rs768840606 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102366349 | GTCTACAAATTCTCT[C/G]ATATCTAGTCATTTG | 51366 |
rs768873931 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102355156 | AAAAAAAAAAAAATC[C/T]ATGCTAAAAAACTGT | 51366 |
rs768881637 | snp | A/G | 3.49016e-05 | 0.00417727 | intron-variant | UBR5 | GRCh38.p7 | 8:102300197 | CTACCATATCTACAC[A/G]TAATGAAACGGTGTA | 51366 |
rs768896521 | snp | C/T | 1.65337e-05 | 0.00287517 | intron-variant | UBR5 | GRCh38.p7 | 8:102295602 | CTGCGCTCTTTTGAT[C/T]TAACTTACTGTATGT | 51366 |
rs768900071 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102379138 | GCTACCTCCTCTCTC[A/G]GTTTCTGAAAGGGGA | 51366 |
rs768901262 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102346647 | TTAATTCCAGCTACT[C/T]GGGAGGCTGAGGCAT | 51366 |
rs768930013 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102335006 | TGGAAAAAGCTTAAG[G/T]GTCCTTCATGGACAA | 51366 |
rs768932075 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102376740 | CGAACTCCTGACCTC[A/G]TGATCTGCCCGCCTA | 51366 |
rs768958391 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102398475 | AATGGACAAATGGGA[G/T]CACGTCAAGTTAAAA | 51366 |
rs768964970 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102353405 | ATGGAATTAGTCCAC[A/C]GCTTGCAAACTTAAA | 51366 |
rs768968023 | snp | C/T | 5.10417e-05 | 0.00505156 | intron-variant | UBR5 | GRCh38.p7 | 8:102259169 | ACTTCATTTTCCATG[C/T]AACATTTATTTATAT | 51366 |
rs768985794 | snp | C/G | 0.000162805 | 0.00902085 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102271214 | CCTTTCCCGGTCTCT[C/G]TCTCCTCGGTTCCTT | 51366 |
rs768992577 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102306833 | ACTACTTAGTTGTGT[C/T]ACAAGCAGAAAAGTT | 51366 |
rs769014141 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102409197 | CAGGCACCTTGTAAT[A/C]ATTCTGGGAAGTCAC | 51366 |
rs769020430 | in-del | -/GTG | 1.64743e-05 | 0.00287 | cds-indel, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102305170 | ATTTCCATCACATCT[-/GTG]GCTGATGAATGTCTG | 51366 |
rs769033041 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102305862 | CTCAAGTAATCCTCC[C/T]GCCTCAGCCTCCCAT | 51366 |
rs769077091 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102259234 | TCTAACAATGCTAGT[C/T]CCCATTTTATGCCAG | 51366 |
rs769077442 | snp | C/T | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102272553 | TGCCTTTGTTGGCAT[C/T]TTGGATACACTCTAG | 51366 |
rs769104121 | in-del | -/TAAAC | 1.85658e-05 | 0.00304673 | intron-variant | UBR5 | GRCh38.p7 | 8:102296863 | AACAGCTTATAATAT[-/TAAAC]TAAAGAAAACTAGAA | 51366 |
rs769106011 | snp | C/T | 1.67475e-05 | 0.00289369 | intron-variant | UBR5 | GRCh38.p7 | 8:102311696 | ACAAAAATGCCATTG[C/T]TGTCCTATCACTTTT | 51366 |
rs769126941 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102285841 | AATTGTGTTTCTCTG[A/G]GATTATATATACTTA | 51366 |
rs769161389 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102354233 | GACAAAATAAGGCAG[A/G]GAGGGACACAAGGAT | 51366 |
rs769161687 | snp | A/C | 1.64871e-05 | 0.00287111 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102326589 | GAAGAAATACCAGCA[A/C]TGGATTTAGGCTTTT | 51366 |
rs769162518 | snp | A/G | 1.65509e-05 | 0.00287666 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102323351 | TTTCCATGTTTTTCA[A/G]GCTTTCAGGAGATCT | 51366 |
rs769197634 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102316518 | AACCAAATTACAGTA[A/C]AAACGATTATTTTTA | 51366 |
rs769209272 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102393418 | AAGATGGGCGGATCA[C/G]GAGGTCAAGAGTTCG | 51366 |
rs769210949 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102332751 | TCATACTTTCAGCCT[A/G]GCACTGATCACATTA | 51366 |
rs769222838 | snp | A/C/T | 6.58972e-05 | 0.00573976 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102288232 | TGTTCATCATGATGA[A/C/T]CCTCTTCTCCAGCCA | 51366 |
rs769244032 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102269521 | GACTTGCTGGAAGAA[A/G]TAATAGTTTTCTGTT | 51366 |
rs769247559 | snp | A/G | 4.96315e-05 | 0.00498129 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285204 | TGAATTCTGAGAAGC[A/G]TGAAGAGGATGATTT | 51366 |
rs769253871 | snp | C/T | 1.64972e-05 | 0.00287199 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102360657 | ACCAATCCTGCAAAC[C/T]CTACCATCCTAAAAG | 51366 |
rs769288852 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311437 | CCTTATTCCTCCCAT[A/G]CAATCTTTGGCCATT | 51366 |
rs769292787 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102261126 | CATTGGATCACACAA[A/C]ACTTTCTAGAAACAC | 51366 |
rs769311834 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102259974 | CGGAGGTTGCACTGA[A/G]CCAAGGTTGTGCCAC | 51366 |
rs769312570 | snp | C/T | 0.000198255 | 0.00995431 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102281496 | GACATCATTCCTTGA[C/T]GGGCGCTAAGCAAGG | 51366 |
rs769312719 | snp | A/C | 1.66244e-05 | 0.00288304 | intron-variant | UBR5 | GRCh38.p7 | 8:102289417 | TTCTTTTCTCATAAA[A/C]TAAAAGCTTTTTAAA | 51366 |
rs769315002 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102325274 | GAAAGTTTTCTGGTT[C/T]GAAGACCAATAGGCA | 51366 |
rs769328645 | snp | G/T | 3.30688e-05 | 0.00406612 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102293620 | CTGCTAGACTGATCA[G/T]ATGATGGTCGTGGTG | 51366 |
rs769340872 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102384270 | TAACTTTACAGCAAT[C/G]ATTCTCATCTTTTCT | 51366 |
rs769351617 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102315508 | TAATCAGAAAAGTCA[C/T]TGATTATTCACAAAT | 51366 |
rs769380039 | in-del | -/TT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102326899 | AATTCATCAATTGCT[-/TT]TTTTTTTTTTTTTTT | 51366 |
rs769402017 | snp | C/T | 1.65007e-05 | 0.00287229 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102270081 | AAGCCTCTCTCCAAG[C/T]GCCTGCCGATGTGCT | 51366 |
rs769415893 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102279002 | AAATAAACCCAATTA[A/G]AAAGAAACCTTAAGA | 51366 |
rs769419406 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102327354 | ATTAAATAAGGTAGA[C/G]AATATTCATACAATG | 51366 |
rs769438789 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102406817 | GTTATGCTTCATATA[A/G]TCCCTGGCATATTTT | 51366 |
rs769439938 | snp | A/C | 1.90914e-05 | 0.00308956 | intron-variant | UBR5 | GRCh38.p7 | 8:102323523 | AGAAAACCACCATCA[A/C]GATGACATAACTTTA | 51366 |
rs769441781 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102291082 | GAATACTCAACCTGT[C/G]TAACTCCCCAGTTAG | 51366 |
rs769469388 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102352348 | ATTAAATCAGCACTT[C/T]TACTTCATAGTTTCC | 51366 |
rs769493156 | snp | A/C | 1.66671e-05 | 0.00288674 | intron-variant | UBR5 | GRCh38.p7 | 8:102311540 | GACTCCTAATCAAAA[A/C]ATGTATCTGATTTTT | 51366 |
rs769494101 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102365468 | AGCAAGACTCCGTCT[-/A]AAAAAAAAAAAAACA | 51366 |
rs769499912 | snp | A/T | 1.70301e-05 | 0.00291801 | intron-variant, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102258974 | TTAAACATTTTTTTT[A/T]AATGTCCTACCTGAT | 51366 |
rs769508443 | snp | A/G | 1.65976e-05 | 0.00288072 | intron-variant | UBR5 | GRCh38.p7 | 8:102259133 | TTTCCTCATTGCCTA[A/G]AGAATTTCAGAAACA | 51366 |
rs769528784 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102408456 | GATATGACAATCTCA[A/G]TAAAGACTGTTTATG | 51366 |
rs769541613 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102373350 | AGTAAGACTATATAT[A/T]CATTCATACAAGAAT | 51366 |
rs769558365 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102383097 | AGACAAGTGGCCAGT[A/G]AGTTCACGACAAGAG | 51366 |
rs769565738 | snp | A/G | 4.94637e-05 | 0.00497287 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102265217 | TCATCACCATCATCT[A/G]TATCATCTAAATCCA | 51366 |
rs769566116 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102340316 | CCCTCATTAGACAAG[C/T]CCCTACTCTTGGCAG | 51366 |
rs769567752 | snp | C/T | 1.65031e-05 | 0.00287251 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102329342 | AAAGTTCTCCTTTAC[C/T]GCTGACAGCCAGAAG | 51366 |
rs769573826 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102365684 | TTCCTTTAAATGTAT[A/G]GATCACTTTACAGAT | 51366 |
rs769582585 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102353033 | CACTCTGGCCTGCTG[C/T]GTGCAGTGTTTTCTC | 51366 |
rs769592420 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102338847 | TCCTGTGATTTCCCA[A/G]TGCCTCCTGTGCTAC | 51366 |
rs769597363 | snp | A/C/G | 3.3058e-05 | 0.00406548 | intron-variant | UBR5 | GRCh38.p7 | 8:102329209 | AAGGATTCTTTGAAA[A/C/G]CATAAAAAAAAATTA | 51366 |
rs769603503 | in-del | -/AT | 1.71687e-05 | 0.00292986 | intron-variant | UBR5 | GRCh38.p7 | 8:102345564 | TAAACAGAAACAAAC[-/AT]CACTGCAGCATACAC | 51366 |
rs769628965 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102343247 | AATTTTTATGAATAA[A/G]TCTTAAATTTTACTG | 51366 |
rs769634033 | snp | G/T | 1.75813e-05 | 0.00296485 | intron-variant | UBR5 | GRCh38.p7 | 8:102265055 | GAAAATCTCATAAAT[G/T]GAAATGTTTTAAAAA | 51366 |
rs769669354 | snp | C/G | 1.64844e-05 | 0.00287087 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102312409 | TCAGCATCTGGACCA[C/G]AGCTGTTCTGACAGT | 51366 |
rs769702760 | snp | C/T | 8.30337e-05 | 0.00644282 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102298458 | CTCGGCCACTTACAG[C/T]TGACATAAATGGGGT | 51366 |
rs769716927 | snp | C/T | 4.94303e-05 | 0.00497119 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311477 | GTACCATTTCCATCT[C/T]GAAGAATAATGGGAG | 51366 |
rs769724973 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102340321 | ATTAGACAAGCCCCT[A/T]CTCTTGGCAGACCAC | 51366 |
rs769727881 | snp | G/T | 1.65932e-05 | 0.00288034 | intron-variant | UBR5 | GRCh38.p7 | 8:102313766 | CCAATATCATTATAA[G/T]TCTGTTAGTAATTAA | 51366 |
rs769729836 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102313675 | TGCAGGGGTGCAACT[A/G]AAGATACCACTGAAG | 51366 |
rs769743048 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102314366 | TCCATGGTGTGGCAG[-/T]TAAGTCTAGGTTTAT | 51366 |
rs769813428 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102349074 | AAGATAACTTTGGAG[A/C]AAAGCAATATAATGC | 51366 |
rs769813773 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102285869 | TTACGTAAATCTAAA[C/T]GGTCAATTGTGGTAC | 51366 |
rs769820825 | in-del | -/T | 0.00793638 | 0.0624916 | intron-variant | UBR5 | GRCh38.p7 | 8:102269154 | ACTCTCTAAAACCTC[-/T]TGTCTAATTACATCT | 51366 |
rs769824804 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102378351 | TTTTGCCATTAAAAT[C/T]GCAAGAACCAGGTCG | 51366 |
rs769835272 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102402558 | CTTCCTAATCTCAAA[C/T]TTAGCTTTTCTTAAG | 51366 |
rs769852472 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102408242 | CATTATAATATTGAT[C/G]TTTTCCCATCTACTG | 51366 |
rs769852847 | in-del | -/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102263192 | TTTCATTATAATGTT[-/G]ATAAGAAAAAACTGG | 51366 |
rs769883674 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102265916 | TATATGTTAGATCTT[C/T]TGAAGTTGTCCCACA | 51366 |
rs769899748 | snp | C/T | 3.29489e-05 | 0.00405874 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102305178 | CACATCTGTGGCTGA[C/T]GAATGTCTGCAGCAT | 51366 |
rs769900558 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102400038 | AAAATATCTGGCATA[A/G]TATGTTACCATTGAA | 51366 |
rs769910879 | snp | C/T | 2.08244e-05 | 0.00322673 | intron-variant | UBR5 | GRCh38.p7 | 8:102286639 | TTTTTATTTTTAAAA[C/T]CAAAAACATTGTGAG | 51366 |
rs769915816 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102367631 | TATATAAACTGAGTC[G/T]TCGGCTTGTGCTGCA | 51366 |
rs769930476 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102299369 | TCTCCTTGAGATAAA[C/G]TGTAGATCTGTAGAA | 51366 |
rs769940371 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102336250 | TTCAAGTGTGCTTTA[C/T]AAATTTTGAATATTA | 51366 |
rs769945418 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102379237 | ACTGCCACCATCTCA[A/G]ACCTGTCCTAGTAAT | 51366 |
rs769948687 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102340818 | TTTGGTATTTAATGG[-/A]AAAAAGAATATAGGT | 51366 |
rs769953660 | snp | A/G | 1.65386e-05 | 0.00287559 | intron-variant | UBR5 | GRCh38.p7 | 8:102295616 | TTTAACTTACTGTAT[A/G]TTCTAAAAATCCCAC | 51366 |
rs769961932 | snp | C/T | | | intron-variant, downstream-variant-500B, nc-transcript-variant | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102251917 | TGCATTAACAAACTT[C/T]ACAAATGAATCTTAC | 51366 |
rs769962802 | snp | C/T | 4.94311e-05 | 0.00497123 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102272596 | TTCATTTGATAAAAA[C/T]GCTTGTGCAATGGCT | 51366 |
rs769965727 | snp | C/T | 2.25375e-05 | 0.00335682 | utr-variant-3-prime, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102254256 | ATGGAAAAAAATCTA[C/T]AAAATTTGCTAGTAA | 51366 |
rs769978138 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102379262 | AGTAATTAATCACTA[C/T]GTTAGGAGAACACAA | 51366 |
rs770028499 | snp | A/G | 1.68196e-05 | 0.00289992 | intron-variant | UBR5 | GRCh38.p7 | 8:102311894 | AGCATGAACACCTTC[A/G]GAAGCACATAAATGA | 51366 |
rs770030992 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102386976 | CAAGACTCCGTCTCA[-/A]AAAAAAAAAAAAAAA | 51366 |
rs770044594 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102409111 | GAGATCAAAATGTCC[A/C]AAGTATCTGAGCACT | 51366 |
rs770077503 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102397718 | CAAACAAAAAAAAAT[A/C]TTTTTCCCACTTCCC | 51366 |
rs770087135 | snp | C/T | 1.67335e-05 | 0.00289248 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102346915 | TACCTGTGAAATCAG[C/T]TCCTCTGGAATGACA | 51366 |
rs770107254 | snp | C/T | 0.00019817 | 0.00995218 | intron-variant | UBR5 | GRCh38.p7 | 8:102289624 | CTGCCACAGCTCAGA[C/T]ATGCAACACATATTT | 51366 |
rs770129473 | in-del | -/TTTT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102380720 | AAAAATTTAACATGC[-/TTTT]TTTTTTTTTTTTTTT | 51366 |
rs770140802 | in-del | -/C | 1.65206e-05 | 0.00287403 | intron-variant | UBR5 | GRCh38.p7 | 8:102295574 | AGGGAGGCTGAAAAG[-/C]TACTCAGCTGTGCTG | 51366 |
rs770158902 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102296177 | GTACACTTGGAAAAC[-/A]ATCAATAACAACAGA | 51366 |
rs770161379 | in-del | -/A | 2.18629e-05 | 0.00330621 | intron-variant | UBR5 | GRCh38.p7 | 8:102286311 | GAACATGCATAATTT[-/A]AAAAAATCTATCTAA | 51366 |
rs770166027 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102268003 | TTTAAGCAATTCTCC[C/T]TGCCTCAGCCTCTCG | 51366 |
rs770167440 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102397288 | TAATTCCTTCTTTAC[A/G]TGTCTGTCTCCTCAT | 51366 |
rs770168628 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102294909 | TTTAAATTCTTTTCT[A/G]GTTTCACAGCAAAGA | 51366 |
rs770180475 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102376171 | CTGTCAAAAATTTAT[C/T]TGTTTCACAAAGTTG | 51366 |
rs770186395 | in-del | -/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102255227 | ATCAATCCATCCCTT[-/C]CATACATACGCATCA | 51366 |
rs770205743 | snp | C/T | 8.25484e-05 | 0.00642397 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102326612 | AGGCTTTTTATTTTT[C/T]GCTCTAGCTTTCTCT | 51366 |
rs770208328 | snp | A/G | 1.6908e-05 | 0.00290753 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102261924 | CTTTACCTGTCCTCC[A/G]CCTTCTTCTTTACAC | 51366 |
rs770209955 | snp | A/T | 3.30246e-05 | 0.0040634 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102347049 | CTGATGACCTACCAG[A/T]GGATCCTCCACCACT | 51366 |
rs770250400 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102273328 | TCCTAACTATATGAA[A/G]TAATGTTTAACTTTG | 51366 |
rs770295306 | snp | A/T | 2.00459e-05 | 0.00316584 | intron-variant | UBR5 | GRCh38.p7 | 8:102312118 | ATATGCCAGCTGAAG[A/T]AGTTTCAAAATTTAC | 51366 |
rs770309411 | snp | C/T | 4.9423e-05 | 0.00497082 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102281405 | GCAAACATCCAAAAC[C/T]GGAAGAACATCAGAA | 51366 |
rs770337391 | in-del | -/ATA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102292156 | TGATATACACCTTCT[-/ATA]ATCCAAGACAAGTGA | 51366 |
rs770341884 | in-del | -/TAAA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102313982 | TTTATAGATTTCATC[-/TAAA]TTTATAAGAAAGACT | 51366 |
rs770344195 | snp | C/G | 1.66969e-05 | 0.00288932 | intron-variant | UBR5 | GRCh38.p7 | 8:102299447 | CAAAGAGTACAGATT[C/G]TTACCTGGAATAGTG | 51366 |
rs770347532 | snp | A/C | 2.34266e-05 | 0.00342239 | intron-variant | UBR5 | GRCh38.p7 | 8:102361544 | TCTTAATAAAGAAAA[A/C]TTGTTGTCAGAAGAT | 51366 |
rs770366138 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102410993 | TAGATCTGAGTCTTA[G/T]ATTCTAAGACATGCT | 51366 |
rs770366592 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102306846 | GTTACAAGCAGAAAA[A/G]TTTACTCTGCATCAT | 51366 |
rs770387018 | snp | C/T | 1.64803e-05 | 0.00287052 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102342516 | CCTAGAGATACTGGA[C/T]TTTGAACAGGTGTAT | 51366 |
rs770406402 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102293088 | ACTAAATATTTGCCA[A/G]AGATCTACAGCATTA | 51366 |
rs770454049 | snp | C/T | 1.68508e-05 | 0.0029026 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102298481 | AATGGGGTCATCCCT[C/T]TTGCATCCCTAAAAT | 51366 |
rs770461466 | snp | A/G | 1.65594e-05 | 0.0028774 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285664 | CTGCTTGCAGATGTT[A/G]GGTAACTGCTGGCGT | 51366 |
rs770461540 | snp | C/T | 1.64811e-05 | 0.00287059 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102277131 | CCTTCTTTTTTTTGC[C/T]GGTTTTGCATGTTCA | 51366 |
rs770464548 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102374847 | ACTTGTACAATCAAA[C/T]ATCTGTCTCCCTCAC | 51366 |
rs770467174 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102299139 | TTACAATTTTTTTTT[A/T]AAAGAATATTCTGGA | 51366 |
rs770469045 | snp | C/T | 1.72469e-05 | 0.00293652 | intron-variant | UBR5 | GRCh38.p7 | 8:102285104 | AAGTTGGGGACGTTC[C/T]GTATATATGAAGAAT | 51366 |
rs770496371 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102291488 | CAGGAATCTCCTCTT[C/T]TGTCCCCCTCACATA | 51366 |
rs770530998 | snp | A/C | 1.67654e-05 | 0.00289524 | intron-variant | UBR5 | GRCh38.p7 | 8:102259155 | TCAGAAACAATAATA[A/C]TTCATTTTCCATGTA | 51366 |
rs770563566 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102361215 | GGGTGGCTGAGAGAT[-/A]AAAAAAAGAAAAAGT | 51366 |
rs770581795 | in-del | -/TA | 1.65266e-05 | 0.00287455 | intron-variant | UBR5 | GRCh38.p7 | 8:102329230 | AAAAAATTACTATTT[-/TA]TATATGTTGATATGT | 51366 |
rs770630542 | snp | C/T | 1.65512e-05 | 0.00287669 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102298907 | GTCACATAACAATTT[C/T]AATATAAAATGAGCA | 51366 |
rs770637097 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102365018 | TAAAGGATCTTCATA[A/C]AATGTTTACGATAGG | 51366 |
rs770640961 | snp | C/T | 1.64855e-05 | 0.00287097 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102360635 | ATCTGTCTGGCTGTA[C/T]TGAAAAACCAATCCT | 51366 |
rs770642499 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102341384 | TGCCAAAGAAAACAG[A/C]ATAACCTTTTGCTTC | 51366 |
rs770645257 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102329581 | CTGGCTCCCTCCATT[A/G]ACTCACTCACCTCCA | 51366 |
rs770655189 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102401421 | CAGGGATGGTATGGG[G/T]TGGCTGCTAATTCCT | 51366 |
rs770670026 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102391004 | GAGGCGGGAGAATCC[C/T]TAGAGCCCAAGAGTT | 51366 |
rs770672466 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102347963 | AGGCATGGTGGCTCA[C/T]GCCTTGTAATCCCAG | 51366 |
rs770689365 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102280848 | TGTCTCTCCAAAACA[C/T]TAAGAAATTAGCCAG | 51366 |
rs770694867 | snp | C/T | 3.31664e-05 | 0.00407211 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102265256 | ACACTTCGACTAGAG[C/T]CATGGCGCTTTCGGT | 51366 |
rs770706096 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102280680 | GAAAAAGCAAATCAC[C/T]TAAGAAATAACGAGC | 51366 |
rs770713583 | snp | C/T | 1.65138e-05 | 0.00287343 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102254471 | ATAGGCTGGAATCCT[C/T]CTTCACTGGCTGGCA | 51366 |
rs770723448 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102398882 | CAAACTATCCACCTG[A/T]TAAGGGATTAATAAT | 51366 |
rs770724192 | in-del | -/CT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102345000 | AAATCCATTCTAGTA[-/CT]AGTTTTTTCACATTT | 51366 |
rs770724570 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102343324 | TTCCTTACCAAAATG[C/T]TTCCCATGGCTATTG | 51366 |
rs770725815 | snp | G/T | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102313893 | TTTCCTCTTCTTTTG[G/T]TGCAGGGGTTGACCG | 51366 |
rs770730433 | snp | A/C/G | 3.30498e-05 | 0.00406497 | intron-variant | UBR5 | GRCh38.p7 | 8:102313781 | TTCTGTTAGTAATTA[A/C/G]GTTTTAGATATCTTG | 51366 |
rs770730964 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102328476 | CTTTAAAGCCAAATC[A/G]ATAATTTGAGACATA | 51366 |
rs770737974 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102290912 | TTTTTTTTTTTTTTT[-/A]AATTTTGGAGTATCT | 51366 |
rs770757156 | snp | A/G | 3.31153e-05 | 0.00406898 | intron-variant | UBR5 | GRCh38.p7 | 8:102295158 | TAAAAGGTCTACACT[A/G]ACGTAGGAAATACAT | 51366 |
rs770765653 | snp | C/T | 9.9739e-05 | 0.00706113 | intron-variant | UBR5 | GRCh38.p7 | 8:102361097 | ACAGTTTATTTTTCA[C/T]TTCTGTATCTTAGAG | 51366 |
rs770765712 | snp | A/G | 1.65828e-05 | 0.00287943 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102329397 | GATGAATTTTGTTCC[A/G]TCCTATAAAGTAAAA | 51366 |
rs770781451 | snp | C/T | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102305186 | TGGCTGATGAATGTC[C/T]GCAGCATCTGTAGAT | 51366 |
rs770782554 | snp | A/G | 1.64781e-05 | 0.00287033 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102266962 | CTGTACCTTTTCTGA[A/G]GAGTCTACTAATCCA | 51366 |
rs770786234 | snp | C/T | | | intron-variant, downstream-variant-500B, nc-transcript-variant | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102252085 | AGTGAAATCATTCCT[C/T]TAAAATACCCTCTCA | 51366 |
rs770794550 | snp | C/T | | | intron-variant, downstream-variant-500B, nc-transcript-variant | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102252139 | ACTGGATAGTCTTGG[C/T]ATCCAGATGATTTAG | 51366 |
rs770805262 | in-del | -/CA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102261700 | AGCAAGACTCCATCT[-/CA]CACACACACACACAC | 51366 |
rs770822673 | snp | A/G | 6.51091e-05 | 0.00570529 | utr-variant-3-prime, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102254271 | CAAAATTTGCTAGTA[A/G]TATTACACAGCAATA | 51366 |
rs770832452 | snp | C/T | 1.65583e-05 | 0.00287731 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102346933 | CTCTGGAATGACAGA[C/T]GCTGGAATAACTGGC | 51366 |
rs770854696 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102410790 | CCTCCCTCTGGGAAG[A/C]GCATGACAAACAGGG | 51366 |
rs770856498 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102290955 | TTTATCAGTTGAGCA[C/T]CCTCAATCCCAAAAT | 51366 |
rs770866603 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102349127 | ACAGCATTTATTTCA[A/G]CTAGTAAATGTCATG | 51366 |
rs770870089 | snp | A/G | 2.32442e-05 | 0.00340904 | intron-variant | UBR5 | GRCh38.p7 | 8:102286653 | ACCAAAAACATTGTG[A/G]GTTTAATAATTAAAA | 51366 |
rs770889597 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102356957 | TAAATGCTAAACTCA[A/G]TGAGCAAAAGTATGA | 51366 |
rs770897777 | snp | C/G | 1.64825e-05 | 0.00287071 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102272628 | TATAAAAACTTCGTG[C/G]TACACCACTGCCCTC | 51366 |
rs770899328 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102402885 | GAAGAAAATAAAAAC[G/T]TATCTACTGATCCAT | 51366 |
rs770908793 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102311580 | TTTATTTCCAAATTA[C/G]ATTTTAGTAATAGTA | 51366 |
rs770922496 | in-del | -/AGAC | 0.000512579 | 0.0160008 | intron-variant | UBR5 | GRCh38.p7 | 8:102295127 | TTGAGGAGAAACGAA[-/AGAC]AGACAGAATGAACTG | 51366 |
rs770938068 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102397351 | CCATCTTTGTATTCC[A/C]GTGTATACACAGGTT | 51366 |
rs770938232 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102273530 | CAATGTCTAGCAAAA[G/T]TATATGCACATGCTC | 51366 |
rs770982917 | snp | A/G | 0.000118595 | 0.00769957 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102293784 | CAATTCTTCCACAGC[A/G]TAAGGTAGCAATGCT | 51366 |
rs770987247 | snp | C/T | 1.74589e-05 | 0.00295451 | intron-variant | UBR5 | GRCh38.p7 | 8:102295813 | ACACAAGTACAAAAA[C/T]TGAAATTTTTTAAAC | 51366 |
rs771001890 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102308114 | TCTTCTAATAGACAA[C/T]TTAAATTTCACCTGT | 51366 |
rs771012573 | snp | A/G | 1.65913e-05 | 0.00288017 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102347072 | CCACCACTTCCACCC[A/G]CTCCAGAACTCCAGC | 51366 |
rs771027765 | snp | A/C | 1.65444e-05 | 0.00287609 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102293673 | TTCTTCACTGCCCTG[A/C]ATGGCATCTATGCTA | 51366 |
rs771030894 | snp | A/C | 1.64863e-05 | 0.00287104 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102305286 | GAATGTGTTGCATTA[A/C]GGTTTGTTTCTGTGC | 51366 |
rs771031590 | snp | A/G | 1.66499e-05 | 0.00288525 | intron-variant | UBR5 | GRCh38.p7 | 8:102280494 | CAAGTGAGTCATTTT[A/G]CTTGAAGTATTTGTA | 51366 |
rs771031612 | snp | C/G | 1.71628e-05 | 0.00292935 | intron-variant | UBR5 | GRCh38.p7 | 8:102287586 | AATACATTTAAATAA[C/G]AAAAAAGCACAAACT | 51366 |
rs771033132 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102383753 | TCCAGAATAAAAGGA[C/T]CCATGAAATATTTGG | 51366 |
rs771033985 | in-del | -/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102336823 | CTTTCACTATTTGGG[-/G]TATTTTATGGTTCTT | 51366 |
rs771053311 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102343623 | TTGGGAGGCCGAGGT[A/G]GGTGGGTCACTTGAG | 51366 |
rs771062234 | in-del | -/A | | | upstream-variant-2KB, nc-transcript-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102412970 | CGGAGAGCACGTGTT[-/A]AGGGAAGGAGGAGGC | 51366 |
rs771092495 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102323617 | AGGTTTCCCAGTATA[A/C]TCTTACCCAATCAAT | 51366 |
rs771097110 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102368829 | TATTATTTAACACAG[C/T]TGCCTCAGCAGCTTC | 51366 |
rs771113813 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102386893 | AGGCAGGAGAACTGC[C/T]TGAACCCAGGAGGCG | 51366 |
rs771119557 | snp | C/T | 0.000115633 | 0.00760283 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102281303 | CCTTTTGCGTTCTAG[C/T]TGAGGTGTATCCAAT | 51366 |
rs771129858 | in-del | -/AA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102355131 | AGATCCTGTCTCTCA[-/AA]AAAAAAAAAAAAAAA | 51366 |
rs771131295 | snp | A/C | 3.30715e-05 | 0.00406628 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102261956 | GGTCAATTGCAAATG[A/C]CAAATCCATTGCTGA | 51366 |
rs771133188 | in-del | -/A | 0.0100735 | 0.0702516 | intron-variant | UBR5 | GRCh38.p7 | 8:102285469 | TCATAATTGACAGCC[-/A]AAAAAAAAATAGTGG | 51366 |
rs771169962 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102356357 | CAGAAGTCTGAGGCA[A/C]GAGAATCACTTGAAC | 51366 |
rs771173439 | snp | C/T | 1.74442e-05 | 0.00295327 | intron-variant | UBR5 | GRCh38.p7 | 8:102262084 | ACCTAAAAAAGTAAT[C/T]ATATGAAACTCAGTT | 51366 |
rs771183866 | snp | A/G | 1.66355e-05 | 0.002884 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102299486 | TGGTCCTTGACCAGT[A/G]CCGGTTGCTGCTGTG | 51366 |
rs771189541 | snp | C/T | 3.29468e-05 | 0.00405861 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102293809 | AATGCTTGGAATACA[C/T]GCTTGCATTTTCCAA | 51366 |
rs771277886 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102333818 | ACTGCAATTTGGCCA[A/C]CTGTGTCCATTCACA | 51366 |
rs771280991 | snp | C/T | 3.48657e-05 | 0.00417512 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102312144 | TTTACCTTTGGAATC[C/T]ACATTCACTGCTAAT | 51366 |
rs771282286 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102376358 | AAGGCTCAATAACTT[A/G]TATTCTGGCTAAATA | 51366 |
rs771287345 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102335046 | GAAAACACACACACA[C/G]AGACACAACAGAAAA | 51366 |
rs771314976 | in-del | -/TACTAGG | | | intron-variant | UBR5 | GRCh38.p7 | 8:102282810 | AATGCAAATCAAAGA[-/TACTAGG]TCACACCCACTGGGA | 51366 |
rs771326154 | in-del | -/AACA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102381593 | GAAACACTGACAAAG[-/AACA]AACATTAATAACCTT | 51366 |
rs771346334 | snp | C/G | 1.64944e-05 | 0.00287175 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102327834 | AAGTTCAGAGTAAGT[C/G]TGAGCAGTGTGCTCT | 51366 |
rs771349387 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102377284 | GCACAGCTCAACAGT[A/G]ACAAACTGCTTTTCC | 51366 |
rs771363018 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102314165 | ATAAACAAGTACAAA[A/G]AAATAGCGTAAAATG | 51366 |
rs771367570 | snp | A/T | 1.64827e-05 | 0.00287073 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102342620 | CCACCTTCGTTCACG[A/T]AAACGTAAAACGGAT | 51366 |
rs771372726 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102282488 | GCCTGGCCAACATGG[A/C]GAAACCCCGTCTCTA | 51366 |
rs771401522 | snp | A/T | 1.66236e-05 | 0.00288297 | intron-variant | UBR5 | GRCh38.p7 | 8:102312260 | CCTGCATGACACAAA[A/T]GGAATTTTGCTTTCA | 51366 |
rs771417798 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102307009 | TCCCTACCTGCGGGA[C/T]GATGACTCTACCTGT | 51366 |
rs771431687 | snp | C/G | 1.7134e-05 | 0.00292689 | intron-variant | UBR5 | GRCh38.p7 | 8:102299978 | TGTTAAACACTAAAT[C/G]AAATTAAATAACAGC | 51366 |
rs771451030 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102332725 | CACTCAGAACCCCTA[C/T]AGCACTTTACTCATA | 51366 |
rs771467187 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102309570 | CCTATCAGGTGCACC[-/T]TTTTTTTTATCCTTT | 51366 |
rs771482012 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102349245 | CAATCCAGGCTGGGC[A/G]TGGTAGCCCACACCT | 51366 |
rs771484444 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102294778 | ATTATTTATTTATGA[C/G]AGGTTCTGAGGGCAC | 51366 |
rs771486796 | snp | A/G | 1.6489e-05 | 0.00287128 | intron-variant | UBR5 | GRCh38.p7 | 8:102295408 | ATAAATGTCTAATTA[A/G]CTCACCTTCAGGACT | 51366 |
rs771510945 | snp | A/G/T | 4.98139e-05 | 0.00499048 | intron-variant | UBR5 | GRCh38.p7 | 8:102361102 | TTATTTTTCATTTCT[A/G/T]TATCTTAGAGTGAAT | 51366 |
rs771516437 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102281251 | AGACCATACCAAGCA[A/G]GTATTTCTTAAATCA | 51366 |
rs771522045 | snp | C/T | 1.66001e-05 | 0.00288094 | intron-variant | UBR5 | GRCh38.p7 | 8:102269116 | GCAAATGCCTGTAAA[C/T]GATGAACAAATGTTA | 51366 |
rs771522984 | snp | A/G | 1.6566e-05 | 0.00287797 | intron-variant | UBR5 | GRCh38.p7 | 8:102295166 | CTACACTAACGTAGG[A/G]AATACATAAATCTAA | 51366 |
rs771527519 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102329792 | ATCCACAGCACTTCA[C/T]AACTTGACATATTTA | 51366 |
rs771532510 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102283900 | TGTTTTTTATTTCAA[C/T]GCTTCTCTCCCCTCC | 51366 |
rs771553395 | in-del | -/CA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102293027 | TTATTAAAACATCAT[-/CA]CACATGCACATGGTT | 51366 |
rs771561358 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102402796 | AGCAGATTCATGCTG[A/G]AGCAGAGCCAATTTC | 51366 |
rs771571621 | in-del | -/ATG | | | intron-variant | UBR5 | GRCh38.p7 | 8:102300630 | ACTAATATCCACACA[-/ATG]ATTAGTTTTAAAACA | 51366 |
rs771578198 | snp | A/G | 1.64811e-05 | 0.00287059 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102267001 | GATACTATCAGCTCC[A/G]TTTTCCCTAAAAACA | 51366 |
rs771579004 | in-del | -/A | 3.30562e-05 | 0.00406534 | intron-variant | UBR5 | GRCh38.p7 | 8:102311509 | TCCTATAATAATGGG[-/A]AAAATGGTAAAGTTT | 51366 |
rs771584549 | in-del | -/AATC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102370523 | ATACAATGTGTTAAT[-/AATC]AAATCAGGGTAATTG | 51366 |
rs771658470 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102343275 | CTGAGGAACCAGACA[C/G]GCTTTTTTTTAAAAA | 51366 |
rs771659142 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102375060 | TTTAAAATGTTTAAA[C/T]GTTTAAAAAGTAATT | 51366 |
rs771694833 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102404348 | CTAATTTGGAAGGGG[-/T]TTTGTTACCACTACA | 51366 |
rs771740106 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102349526 | TCTCACAGAAAGAGA[C/T]AAGAGGAGAGAAAGG | 51366 |
rs771747346 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102267289 | GCTGGAACACTTCTA[C/T]AATGCTCAGAGGGAG | 51366 |
rs771753861 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102403927 | AAGCATTACAGTGAG[A/G]GAAAGCAGAACAATG | 51366 |
rs771762177 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102255017 | ATCATTTTATAATAG[C/T]AATTATTGGGGAACA | 51366 |
rs771777318 | snp | A/G | 3.32e-05 | 0.00407417 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295277 | GTAGAACACGCTCCA[A/G]TGCAAGCTGGGCAAA | 51366 |
rs771782262 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102400975 | TGTTAAGACAAAGAA[A/G]AGAGGGTAAAAGAGC | 51366 |
rs771791801 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102312782 | GAAATCCTCCCATCT[C/T]CTAATTAAATTAAAG | 51366 |
rs771795960 | snp | A/C | 1.65154e-05 | 0.00287358 | splice-donor-variant | UBR5 | GRCh38.p7 | 8:102342472 | AATTTTTTCCAAATA[A/C]CTTATCAGGCCACCA | 51366 |
rs771821298 | snp | C/G | 1.65833e-05 | 0.00287948 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102254485 | TTCTTCACTGGCTGG[C/G]AGTGATGGGCTTGAT | 51366 |
rs771866494 | snp | A/T | 3.33778e-05 | 0.00408507 | intron-variant | UBR5 | GRCh38.p7 | 8:102311251 | TTCAAGACTATTTAG[A/T]GGTGTTTTGTGAATT | 51366 |
rs771896833 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102336645 | GTGCCCTTGTCAAAA[A/C]TTAGTTAATAATATA | 51366 |
rs771897952 | snp | C/T | 1.75268e-05 | 0.00296025 | intron-variant | UBR5 | GRCh38.p7 | 8:102287604 | AAAAGCACAAACTCA[C/T]TATGGTTTAAAACAG | 51366 |
rs771906891 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102268037 | AGCTGGGATTACAGG[C/T]GCTCACCACCACACC | 51366 |
rs771911206 | snp | C/T | 1.67351e-05 | 0.00289263 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102257692 | GAACCAACGCTTGAA[C/T]TGCAGAAGCTTCTCA | 51366 |
rs771917657 | snp | A/T | 2.23821e-05 | 0.00334523 | intron-variant | UBR5 | GRCh38.p7 | 8:102297026 | GAATAATTATAAGTA[A/T]GCATATATCTCATCA | 51366 |
rs771920356 | in-del | -/A | | | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102410914 | AGAGAGCAGTGAAGT[-/A]ACTGGGAGAGAGGAA | 51366 |
rs771920873 | snp | G/T | 1.64784e-05 | 0.00287035 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102342590 | CCTTTCATTATCAAA[G/T]GAGGCTCCATCAAGC | 51366 |
rs771922536 | snp | A/C/G | 4.95645e-05 | 0.00497797 | intron-variant | UBR5 | GRCh38.p7 | 8:102313935 | AGACAACAACAAAAT[A/C/G]GTAAGTACCAAAAAG | 51366 |
rs771929315 | snp | C/T | 1.67091e-05 | 0.00289038 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102347087 | ACTCCAGAACTCCAG[C/T]GGCTTCTAAATATTG | 51366 |
rs771951023 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102253579 | GAAGTGCAGTAACCT[C/T]TTGAGACTGACTGCT | 51366 |
rs771959837 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102384014 | TTATTCCCAACCAGA[A/G]ATCATATATCTAGCC | 51366 |
rs771966683 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102369160 | TTCTGCCTTTATCTA[C/T]CACAATATATTGTTT | 51366 |
rs771969775 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303169 | CAAACACTTTGTCTG[C/T]CTAGCATAGTCCTGA | 51366 |
rs771973720 | snp | C/T | 1.67374e-05 | 0.00289282 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102314751 | AAACTTACTGTATGG[C/T]ATTGATGCACTGCTG | 51366 |
rs771985067 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102272187 | ATAGCATTTTCTTCT[C/T]AAATATCCCTGTGGG | 51366 |
rs771990390 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102319080 | GGATCAAATTCACAC[A/G]TAACAATATTAACTT | 51366 |
rs772006752 | snp | C/T | 1.64849e-05 | 0.00287092 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102281335 | TTGTCTGCTGATTCA[C/T]TGCCTTAATCCAGTA | 51366 |
rs772016544 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102289596 | AAAGAATCAGAAGCT[C/T]ATGAGTGGGCTCCTG | 51366 |
rs772023568 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102337606 | AAGTCAGCCTCATAT[A/G]CCAGGAATAAATTCC | 51366 |
rs772029082 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102412154 | CCCCCCGCGCCCGCC[A/G]ACCCGCCAGCCCTAT | 51366 |
rs772045405 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102324286 | TTCTTTATCCCAGAA[G/T]ACTACTGTTTCCTGC | 51366 |
rs772047881 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102386485 | TATACATAGTCTCCT[A/C]TCCTCCATCAAACCC | 51366 |
rs772052229 | snp | C/T | 1.64833e-05 | 0.00287078 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102360112 | TAGAGTCTCAGAACC[C/T]GAGAGAAACCATGGA | 51366 |
rs772057591 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102301411 | ATATTTGCCATTATA[C/G]TATTCACTATTAAAA | 51366 |
rs772072677 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102262799 | CCTCCGGAAAAAACT[A/G]TAACATAAATCCTCA | 51366 |
rs772098686 | snp | A/C/G | 6.6585e-05 | 0.00576963 | intron-variant | UBR5 | GRCh38.p7 | 8:102272792 | TAAAACACATCAAGA[A/C/G]GTCAAAAAGTAGTAA | 51366 |
rs772160424 | snp | C/G | 1.66239e-05 | 0.00288299 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285709 | GCAGCTGCTGCAGCT[C/G]CAGCACTTGTACTGA | 51366 |
rs772161199 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102296301 | AATTACTTAATGGTA[C/T]GGTAGATGGTTTTTA | 51366 |
rs772162409 | snp | C/T | 1.65124e-05 | 0.00287331 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102294001 | TCAGAATAACAAAAA[C/T]TCTTGCCACTGAACG | 51366 |
rs772172757 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102379219 | GCCAGATGCTCTTTG[-/T]TAACTGCCACCATCT | 51366 |
rs772191707 | snp | A/G | 1.65485e-05 | 0.00287645 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102312347 | TTACACTTACCTGCA[A/G]TTCATCAATTCTAAG | 51366 |
rs772220824 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102324854 | CTTGTTCTGCAGCTG[-/T]TAACTGCCCTCAGCC | 51366 |
rs772248436 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102377391 | ATAATAATCCACTGT[A/G]CCTAAAATCATATCG | 51366 |
rs772255452 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102274404 | TTGGGAAGTTGGCTA[A/T]TCAGTTTGAAAGAAA | 51366 |
rs772257718 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102274209 | AATCATTTTGTTAGT[A/G]GTAGTGTTGATGTTA | 51366 |
rs772257826 | snp | C/T | 1.65285e-05 | 0.00287471 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102275590 | GAATTTTGATTCTTT[C/T]ACCTCAAAACCACCC | 51366 |
rs772260922 | in-del | -/AA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102390474 | GCGAGACTCTGTCTC[-/AA]AAAAAAAAAAAAAAA | 51366 |
rs772290540 | in-del | -/T | 1.65868e-05 | 0.00287978 | intron-variant | UBR5 | GRCh38.p7 | 8:102270020 | CAGTTAAGAGGTAAC[-/T]TAAGTACACAGTACA | 51366 |
rs772292380 | snp | C/T | 1.66441e-05 | 0.00288474 | intron-variant | UBR5 | GRCh38.p7 | 8:102312283 | TGCTTTCAAACTCCA[C/T]AATAAACTCACGGAG | 51366 |
rs772299966 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102376167 | ACTTCTGTCAAAAAT[G/T]TATCTGTTTCACAAA | 51366 |
rs772304353 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102388954 | GTAGTTACACTTCCA[C/T]AATATGTATTATTCT | 51366 |
rs772312398 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102312323 | ATATTCACTTGCTGA[A/G]TAACTTCTTTACACT | 51366 |
rs772312955 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102413285 | TTTGCAGCAACTTCT[A/G]TTACCTCGGTCTCCC | 51366 |
rs772314058 | snp | A/T | 4.9703e-05 | 0.00498488 | intron-variant | UBR5 | GRCh38.p7 | 8:102279000 | GAAAATAAACCCAAT[A/T]AGAAAGAAACCTTAA | 51366 |
rs772332528 | snp | C/T | 1.6492e-05 | 0.00287154 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102270099 | CTGCCGATGTGCTGG[C/T]AAAGGCTCAGGATCA | 51366 |
rs772355096 | snp | C/T | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102345519 | GGGCAGAATGAATGT[C/T]GGCATCAAGGAGAGA | 51366 |
rs772364210 | snp | A/G | 2.83539e-05 | 0.00376512 | intron-variant | UBR5 | GRCh38.p7 | 8:102264573 | CCTAAAAACAAACAC[A/G]GAGAAATAAGATTTA | 51366 |
rs772365538 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102261509 | AGATCGAGACCATCC[C/T]GGCCAACATGGTGAA | 51366 |
rs772369120 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102378013 | ATGGGTCTAAAGGCT[A/G]TATCAAATGGCTCTT | 51366 |
rs772370174 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102280035 | AACTGGTAATTCTCA[-/T]TTTCTTGATTAAATC | 51366 |
rs772403668 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102316427 | CACATATCTATACTG[C/G]TCACCTATTTTTATA | 51366 |
rs772416344 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102346126 | TCTACAGTGAAAAAT[A/G]TCTACCACCTTGAAA | 51366 |
rs772428722 | snp | C/T | 1.6703e-05 | 0.00288985 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102300010 | CTTACCAGGATCCAT[C/T]GCAGGAGGGTCAGGA | 51366 |
rs772434686 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102345231 | CTAAAATACTATTGT[C/G]GCTCTTCAAAATAAA | 51366 |
rs772442701 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102353203 | CAGTACTGGAATCAG[C/T]TGATTCCTTTTATCT | 51366 |
rs772494117 | snp | A/T | 5.00079e-05 | 0.00500015 | intron-variant | UBR5 | GRCh38.p7 | 8:102279216 | AGTAGCACCTAAACA[A/T]AAAAAGATAAAATGT | 51366 |
rs772504024 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102407025 | GTAGTGAGTAGCTAC[A/G]TGGCACTACAGTGCA | 51366 |
rs772508092 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102284812 | GAGGCCAGGGTGGGC[A/G]GATCACAAGGTCAGG | 51366 |
rs772509787 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102269606 | ACTAATTTGTGTTTC[A/G]TATCATATAAAGAAA | 51366 |
rs772512810 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102304755 | CTCCTCTACATTCTA[A/C]AAATTTAGATAAAAG | 51366 |
rs772535146 | snp | A/G | | | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102293810 | ATGCTTGGAATACAC[A/G]CTTGCATTTTCCAAT | 51366 |
rs772540993 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102333984 | TTTCCAGATGTCAAT[A/C]AAAACAAAACAAAGA | 51366 |
rs772548508 | snp | A/G | | | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102286420 | GATGCTGGGTGTTGC[A/G]GACAGCCCACTGCAT | 51366 |
rs772553054 | snp | A/G | 1.71873e-05 | 0.00293144 | intron-variant | UBR5 | GRCh38.p7 | 8:102300187 | TCAGAGCTCACTACC[A/G]TATCTACACATAATG | 51366 |
rs772571631 | snp | A/G | 1.66563e-05 | 0.0028858 | intron-variant | UBR5 | GRCh38.p7 | 8:102346226 | AAAAACATGACGGTG[A/G]TCCACCAACCTCCAG | 51366 |
rs772572304 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102366279 | TTCCCACCCAGTTCA[A/T]ATGCCACCTCCTCCA | 51366 |
rs772635553 | snp | A/T | 4.04016e-05 | 0.00449435 | intron-variant | UBR5 | GRCh38.p7 | 8:102323540 | ATGACATAACTTTAA[A/T]AATATATATAATATT | 51366 |
rs772642519 | in-del | -/C | 6.65613e-05 | 0.00576855 | intron-variant | UBR5 | GRCh38.p7 | 8:102311536 | TTTGACTCCTAATCA[-/C]AAAAATGTATCTGAT | 51366 |
rs772654944 | snp | C/G | 1.6531e-05 | 0.00287493 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102259011 | TTGAAAGAGGTAAAA[C/G]TGATCAGCATTTGCA | 51366 |
rs772669678 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102315637 | AAGAAAACTGGTATT[A/G]TTTTCACCAGGATCT | 51366 |
rs772672859 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102400090 | TGGTACCCCTCTGTA[A/C]CAATTTTGCATCTTC | 51366 |
rs772678133 | in-del | -/ACACATATAT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102396662 | TATACACACACACAC[-/ACACATATAT]ATATATATACACACA | 51366 |
rs772681413 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102395335 | GAACTGACAGGCAGC[A/G]GACGCCCCCAAATCT | 51366 |
rs772684111 | snp | A/G | 1.65168e-05 | 0.00287369 | intron-variant | UBR5 | GRCh38.p7 | 8:102289439 | CTTTTTAAATCTACC[A/G]CAATTAAAATCACCT | 51366 |
rs772724480 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102264030 | AAGCCACCGTGCCTG[G/T]CCTGGAAGGCTCTTT | 51366 |
rs772728772 | snp | C/G | 1.65332e-05 | 0.00287512 | intron-variant | UBR5 | GRCh38.p7 | 8:102295592 | CTCAGCTGTGCTGCG[C/G]TCTTTTGATTTAACT | 51366 |
rs772737208 | snp | G/T | 1.66051e-05 | 0.00288137 | intron-variant | UBR5 | GRCh38.p7 | 8:102289423 | TCTCATAAAATAAAA[G/T]CTTTTTAAATCTACC | 51366 |
rs772738724 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102270589 | CAATGGCATAATCTC[A/G]GCTCACTGCAACCTC | 51366 |
rs772741354 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102289943 | GTGATCTAACTTTTA[A/T]GAGATCTGACATGAT | 51366 |
rs772749115 | in-del | -/AAA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102355130 | GAGATCCTGTCTCTC[-/AAA]AAAAAAAAAAAAAAA | 51366 |
rs772754805 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102291210 | TTTGGGGACTTCTAG[G/T]TCCAGCAATTTGGCA | 51366 |
rs772784442 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102382175 | CTGCCACGGGTCCAA[C/T]TCAATTAACAAATAC | 51366 |
rs772785889 | snp | C/T | 3.31664e-05 | 0.00407211 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102258996 | CTACCTGATTCATCA[C/T]TGAAAGAGGTAAAAC | 51366 |
rs772791504 | snp | C/T | 1.66095e-05 | 0.00288175 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102298459 | TCGGCCACTTACAGC[C/T]GACATAAATGGGGTC | 51366 |
rs772798699 | snp | A/G | 3.29473e-05 | 0.00405864 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311447 | CCCATGCAATCTTTG[A/G]CCATTGGGTAGATGG | 51366 |
rs772809009 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102327200 | TGTGCCTGGGCCTAA[A/C]AGACATATTTTCTTC | 51366 |
rs772822140 | snp | A/T | 3.50103e-05 | 0.00418377 | intron-variant | UBR5 | GRCh38.p7 | 8:102265066 | AAATTGAAATGTTTT[A/T]AAAAATTCAAACCCA | 51366 |
rs772827827 | snp | A/T | 3.31587e-05 | 0.00407164 | intron-variant | UBR5 | GRCh38.p7 | 8:102275636 | TTAAAAAAAAAAAAA[A/T]GCATGACAGATTATT | 51366 |
rs772837909 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102390265 | GTGGCTCACGCCTGT[A/C]ATCCCAGTACTTTGG | 51366 |
rs772847785 | snp | C/T | 1.64806e-05 | 0.00287054 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102360159 | CAGGCCTTGACGTCC[C/T]CCCTGCCCCCGAGTT | 51366 |
rs772859487 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102394302 | CCTGACCTCATCATC[C/T]GTCCGCCTTGGCCTC | 51366 |
rs772885338 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102340351 | CTCTCATCTGGTGCT[G/T]GTACCTCTTCTCACC | 51366 |
rs772895438 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102371691 | CGTCCCTGGTTCAAG[C/T]GATTCTCCTGCCTCA | 51366 |
rs772912496 | snp | A/C | 3.32447e-05 | 0.00407691 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102275822 | TCCCATAAAGCTACA[A/C]TGTGGCCTGTAAGAA | 51366 |
rs772926760 | snp | A/G | 1.64849e-05 | 0.00287092 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102360100 | TGCCAGCCTGCCTAG[A/G]GTCTCAGAACCTGAG | 51366 |
rs772973185 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102275150 | AAGAAGACACAATCT[A/G]AGCATCAATATGAAT | 51366 |
rs772994063 | snp | A/G | 6.60284e-05 | 0.00574542 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102347044 | TCCAGCTGATGACCT[A/G]CCAGAGGATCCTCCA | 51366 |
rs773013513 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102299374 | TTGAGATAAAGTGTA[A/G]ATCTGTAGAACCCTA | 51366 |
rs773017226 | snp | C/G/T | 4.9576e-05 | 0.00497855 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102294051 | GCAATAGCTTCTTCT[C/G/T]TACGTCCAGGTGTAT | 51366 |
rs773073823 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102285062 | ACAAACAAACAAACA[A/C]AAAATTGTAAGTTGA | 51366 |
rs773083999 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102373386 | TATGCTAGCAGATAA[C/G]ACCGAAAGACTTCTT | 51366 |
rs773087716 | snp | A/G | 1.64985e-05 | 0.0028721 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102265232 | GTATCATCTAAATCC[A/G]TATCTACTACACTTC | 51366 |
rs773100541 | in-del | -/TT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102330023 | AAACAAGTGCCCATA[-/TT]TTTAAGGTAATCATT | 51366 |
rs773104160 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102370300 | CCTCCTAAGTAGCTG[-/A]AGATTACAAGCACAC | 51366 |
rs773112124 | snp | A/C/T | 6.6407e-05 | 0.00576192 | intron-variant | UBR5 | GRCh38.p7 | 8:102280483 | CTTTAAAAAGACAAG[A/C/T]GAGTCATTTTACTTG | 51366 |
rs773116700 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102401194 | TAAAAAAGCTTAACC[A/G]TATCATGTCCCCGAT | 51366 |
rs773125308 | snp | C/T | 1.67584e-05 | 0.00289464 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102304011 | CTTGGTTTTTTCCTC[C/T]AATTAAAGTTTCCTG | 51366 |
rs773176559 | snp | C/T | 1.71363e-05 | 0.00292709 | intron-variant | UBR5 | GRCh38.p7 | 8:102294931 | CAGCAAAGAAGAGTA[C/T]TTGAAAAACATACTT | 51366 |
rs773192296 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102398649 | AGCCGGGCATGGTGG[C/T]GGGCGCCTGTAATCC | 51366 |
rs773193526 | snp | C/T | 3.30737e-05 | 0.00406642 | intron-variant | UBR5 | GRCh38.p7 | 8:102295617 | TTAACTTACTGTATG[C/T]TCTAAAAATCCCACT | 51366 |
rs773194319 | snp | C/T | 9.95421e-05 | 0.00705416 | intron-variant | UBR5 | GRCh38.p7 | 8:102313767 | CAATATCATTATAAT[C/T]CTGTTAGTAATTAAG | 51366 |
rs773242734 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102267062 | CTTCTAGAATTTAGC[A/G]TATAATTTAAATTTA | 51366 |
rs773244266 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102378371 | GAACCAGGTCGGGTG[C/T]GGTGGCTCACACCTG | 51366 |
rs773253948 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102396285 | TATCTATAGCTCTAC[A/G]GTCACACAGATTCAA | 51366 |
rs773255342 | snp | A/G | 2.23776e-05 | 0.00334489 | utr-variant-3-prime, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102254258 | GGAAAAAAATCTACA[A/G]AATTTGCTAGTAATA | 51366 |
rs773255658 | in-del | -/ATT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102255716 | TTGCAGGACTAATTA[-/ATT]CATGGGAGAACTGTT | 51366 |
rs773260793 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102310909 | ATTCTGGTCATATCA[A/C]AAAAAAGTACTTTCT | 51366 |
rs773274002 | snp | A/G | 3.29592e-05 | 0.00405938 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102272612 | GCTTGTGCAATGGCT[A/G]TATAAAAACTTCGTG | 51366 |
rs773282888 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102379290 | CAAATGTTTGTAAAA[C/T]GCGGTCGCCATCATC | 51366 |
rs773285260 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102336253 | AAGTGTGCTTTATAA[A/C]TTTTGAATATTAACT | 51366 |
rs773291398 | snp | A/T | 6.72834e-05 | 0.00579976 | intron-variant | UBR5 | GRCh38.p7 | 8:102271262 | TAGAAGAAAATCAGA[A/T]ATATACTGTATTTAG | 51366 |
rs773292336 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102412074 | CAGCTGGCCGGCCGG[C/T]GCGTAAACACCCGCA | 51366 |
rs773300900 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102290804 | CAAAAAATTTAAAAA[C/G]AGTAATTTAAAAATA | 51366 |
rs773301722 | in-del | -/CA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102386974 | AGCAAGACTCCGTCT[-/CA]AAAAAAAAAAAAAAA | 51366 |
rs773306605 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102289156 | GGTGACAGAGCGAGA[C/T]TCTGTCTCCAAAAAA | 51366 |
rs773309144 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102286000 | CACGCCACCTCCCCC[C/T]GCCAAAGGGGCTACA | 51366 |
rs773310205 | in-del | -/TTGT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102406282 | AGTATTGGTTTTTTA[-/TTGT]TTGTTTTTGGTTTTG | 51366 |
rs773322189 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102265960 | CTGTCCTTTTGTTTT[A/C]AAATATTTTCTCTAT | 51366 |
rs773335736 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102390025 | CGGCCTCCCAAAGTG[C/T]TGGGATTACAGGCGT | 51366 |
rs773341835 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102367657 | CTGCATCATGGATTT[C/G]TTTCTGGGTGAAGGG | 51366 |
rs773348717 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102408257 | CTTTTCCCATCTACT[C/G]TCTCAACTGTTCCTC | 51366 |
rs773358926 | snp | A/G | 3.38931e-05 | 0.00411648 | intron-variant | UBR5 | GRCh38.p7 | 8:102295787 | TCCGTTTGAGTCTAT[A/G]GAGAATTTATACACA | 51366 |
rs773379733 | snp | C/T | 1.66857e-05 | 0.00288835 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102346390 | GCCTTGTAAAACAAC[C/T]TGGGCCTGAAATAAA | 51366 |
rs773381417 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102397346 | GCCAGCCATCTTTGT[A/G]TTCCAGTGTATACAC | 51366 |
rs773412971 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102294924 | AGTTTCACAGCAAAG[A/C]AGAGTACTTGAAAAA | 51366 |
rs773428460 | snp | C/T | 1.6607e-05 | 0.00288153 | intron-variant | UBR5 | GRCh38.p7 | 8:102326525 | CGAGGTCCCTTAAGA[C/T]AGGCTAAATCCATCA | 51366 |
rs773432747 | snp | A/G | 1.65999e-05 | 0.00288091 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102346927 | CAGCTCCTCTGGAAT[A/G]ACAGATGCTGGAATA | 51366 |
rs773433910 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102384466 | CAGCACTCAGGGAGG[A/C]CAAGGCAGGAGGAAC | 51366 |
rs773437324 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102375089 | TTTTTGGCCGGGCAC[A/G]GTGGCTCACACCTGC | 51366 |
rs773440797 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102379248 | CTCAAACCTGTCCTA[C/G]TAATTAATCACTATG | 51366 |
rs773470287 | snp | A/G | 3.76797e-05 | 0.00434033 | intron-variant | UBR5 | GRCh38.p7 | 8:102312128 | TGAAGAAGTTTCAAA[A/G]TTTACCTTTGGAATC | 51366 |
rs773479150 | snp | C/T | 1.68216e-05 | 0.00290009 | intron-variant | UBR5 | GRCh38.p7 | 8:102261275 | CTGTGAAAAATTTAC[C/T]AGTGCTATTTAAAGG | 51366 |
rs773495698 | snp | C/G | 3.38009e-05 | 0.00411088 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102261925 | TTTACCTGTCCTCCA[C/G]CTTCTTCTTTACACA | 51366 |
rs773506982 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102336259 | GCTTTATAAATTTTG[A/T]ATATTAACTCCTTAT | 51366 |
rs773521136 | snp | C/T | 1.66443e-05 | 0.00288477 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102299469 | GGAATAGTGGAGGTG[C/T]TTGGTCCTTGACCAG | 51366 |
rs773533287 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102306891 | GTCAGTTATTCTTAT[A/G]GCAAAAGGCAGAGTG | 51366 |
rs773553498 | in-del | -/AG | 3.30502e-05 | 0.00406497 | intron-variant | UBR5 | GRCh38.p7 | 8:102272518 | CTGCTTGTTATTTGT[-/AG]AGTACTTACTTGTGT | 51366 |
rs773559407 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102356726 | GATCGCGCCACTGCA[A/C]TCCAGCCTGGGTGAC | 51366 |
rs773566265 | snp | A/G | 1.64798e-05 | 0.00287047 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102342522 | GATACTGGACTTTGA[A/G]CAGGTGTATTCTTCT | 51366 |
rs773569715 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102306170 | ACAAATAGCATGAAT[A/G]TACCAAGAAGTTCAT | 51366 |
rs773571573 | in-del | -/T | 0.000339131 | 0.0130173 | intron-variant, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102258966 | TTCATTCTTTAAACA[-/T]TTTTTTTAAATGTCC | 51366 |
rs773575916 | snp | C/T | 9.96992e-05 | 0.00705972 | missense, nc-transcript-variant, intron-variant | UBR5 | GRCh38.p7 | 8:102285262 | AATGCAGAACCATAA[C/T]GTAATTGAGCTTCAG | 51366 |
rs773582986 | snp | C/T | 1.68309e-05 | 0.00290089 | intron-variant | UBR5 | GRCh38.p7 | 8:102285468 | TCTCATAATTGACAG[C/T]CAAAAAAAAATAGTG | 51366 |
rs773585755 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102392852 | AGATGACACTCACAA[C/G]CACAAACTGAAGGAA | 51366 |
rs773607211 | in-del | -/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102363268 | GTGATTTGGCCCCCA[-/G]AAAAATACATTTTCA | 51366 |
rs773610829 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102333332 | GTTTTTATGAAGTAC[A/G]AATTGCTGCTTCTTA | 51366 |
rs773636860 | snp | C/T | 6.61802e-05 | 0.00575202 | intron-variant | UBR5 | GRCh38.p7 | 8:102361117 | GTATCTTAGAGTGAA[C/T]AATTTACCTCAAGAA | 51366 |
rs773644564 | snp | C/G | 1.65414e-05 | 0.00287583 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102298940 | CGCCTTTCGATCCTT[C/G]GATTCTACTACAGAT | 51366 |
rs773658364 | snp | A/G | 9.89332e-05 | 0.00703255 | intron-variant | UBR5 | GRCh38.p7 | 8:102267039 | TTTCACATTCCAGAT[A/G]ACGGAGACTTCTAGA | 51366 |
rs773672227 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102389582 | TTTGGGTTGGTTTAC[C/T]GCCCAGCAATAAAAA | 51366 |
rs773689752 | snp | G/T | 2.33637e-05 | 0.00341779 | intron-variant | UBR5 | GRCh38.p7 | 8:102361545 | CTTAATAAAGAAAAA[G/T]TGTTGTCAGAAGATT | 51366 |
rs773699516 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102282394 | ATGGGCAAGGTCAGG[C/T]GCAGTGGCTCACACC | 51366 |
rs773760171 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102276374 | AAAGTGATCAAGTCC[A/G]TCTTAAGTTTCTCTT | 51366 |
rs773761199 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102373209 | CGAAACAGGAAAAGG[-/A]AAAGAATGCACATGC | 51366 |
rs773775536 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102331536 | CAGACACACTGGATG[A/C]AACTCCTTCCCATAT | 51366 |
rs773784979 | in-del | -/AACAAGCATGTTACCATGGGTA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102335263 | TGGTTACCATGGGCT[-/AACAAGCATGTTACCATGGGTA]GACAAGCAGTGTGGG | 51366 |
rs773809832 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102376237 | TGTGTACTCTCTAAA[A/G]TAAGAGTGCCTAAAT | 51366 |
rs773811223 | snp | A/T | 1.65457e-05 | 0.00287621 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102298912 | ATAACAATTTCAATA[A/T]AAAATGAGCATTCGC | 51366 |
rs773826633 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102401496 | GTATGTACTCTTCAG[C/T]AGCTCTCAGCTCTCA | 51366 |
rs773865003 | snp | A/C | 1.65315e-05 | 0.00287498 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285195 | TCTTCTCGCTGAATT[A/C]TGAGAAGCGTGAAGA | 51366 |
rs773872579 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102266085 | TTTTTCTTTTAGATA[C/T]TGCCCTTTTAATTCT | 51366 |
rs773890225 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102293137 | CCTAAACCAGCAGAA[C/T]TGGCATCACCTGAGA | 51366 |
rs773921443 | snp | A/G | 1.65762e-05 | 0.00287886 | intron-variant | UBR5 | GRCh38.p7 | 8:102278778 | TATATGCTGGGACAA[A/G]TTGTCCTTAATAAAT | 51366 |
rs773925647 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102279491 | CAGCATTTAATAATA[C/T]TGTGCCATTTTGTAT | 51366 |
rs773928361 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102372047 | ACTCCAGCCTGGACA[A/C]AGAGCTTAGCAACTA | 51366 |
rs773934737 | snp | C/G | 1.94619e-05 | 0.00311938 | intron-variant | UBR5 | GRCh38.p7 | 8:102298499 | GCATCCCTAAAATAA[C/G]AAAAATTATATGTAA | 51366 |
rs773943926 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102328519 | TGTCAATCTGTATTT[C/T]CTAGCTTCTCAACAT | 51366 |
rs773944984 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102340430 | CACCTACCTCTCTAT[C/T]CCCTATCAAGCCTTC | 51366 |
rs773946474 | snp | A/C | 1.98269e-05 | 0.0031485 | utr-variant-3-prime, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102254283 | GTAATATTACACAGC[A/C]ATACACACTTTTTAT | 51366 |
rs773949188 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102402766 | CTGGAATACCTCATC[A/G]CCTGAATTCTGAACA | 51366 |
rs773950070 | snp | A/C | 3.31994e-05 | 0.00407414 | intron-variant | UBR5 | GRCh38.p7 | 8:102360239 | CAACATTTTTTACAA[A/C]CCTGTTATTTCAAAT | 51366 |
rs773965544 | snp | G/T | 4.95242e-05 | 0.0049759 | intron-variant, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102276959 | AATAAAAACAAAGGG[G/T]CTTAGCAAATACCTG | 51366 |
rs773965753 | snp | A/C | 1.73863e-05 | 0.00294836 | intron-variant | UBR5 | GRCh38.p7 | 8:102265074 | ATGTTTTAAAAAATT[A/C]AAACCCAAGATTAAA | 51366 |
rs774063526 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102349381 | AAAATTAGCCAGCCA[C/T]GGTGGCACTCACGTG | 51366 |
rs774067064 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102379542 | CTCCTTCTTACCCTG[A/C]CCACTCCACCAACCC | 51366 |
rs774067192 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102335665 | GTGATTCTTGTGCCT[C/T]AGCCTCCCAAGTAGC | 51366 |
rs774089369 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102409283 | ATCCTGGCATCATTA[C/T]TATTCATTATTGGCA | 51366 |
rs774089445 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102288488 | GGGCGGATCACAAGG[G/T]CAAGAGATCAAGACC | 51366 |
rs774095970 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102398995 | ATTTCCCAAAAGACA[C/T]ATAAATGGCAAACAG | 51366 |
rs774112103 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102380116 | AACAGCAAAGAGGCC[A/G]GGCGCGGTGGCTCAG | 51366 |
rs774125267 | snp | A/G | 1.662e-05 | 0.00288266 | intron-variant | UBR5 | GRCh38.p7 | 8:102329404 | TTTGTTCCATCCTAT[A/G]AAGTAAAATACAATA | 51366 |
rs774125399 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102311584 | TTTCCAAATTAGATT[C/T]TAGTAATAGTAATAA | 51366 |
rs774132346 | in-del | -/CACA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102351414 | GAAATAAGCCTGTCA[-/CACA]CACACACACACACAA | 51366 |
rs774151375 | snp | C/T | 1.65168e-05 | 0.00287369 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102254473 | AGGCTGGAATCCTTC[C/T]TCACTGGCTGGCAGT | 51366 |
rs774153339 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102348009 | AGGCAGGTGGATCAC[A/G]AGGTCAGGAGTTCAA | 51366 |
rs774156394 | snp | A/G | 4.99172e-05 | 0.00499561 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102299489 | TCCTTGACCAGTACC[A/G]GTTGCTGCTGTGGTA | 51366 |
rs774158082 | snp | A/G | 3.2956e-05 | 0.00405918 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102286529 | CTCCTGTTCTATGTC[A/G]TCACTCTGACTACTA | 51366 |
rs774158652 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102253394 | AAATGTAACAAGATA[C/T]TTAAAAAAGGCTAGA | 51366 |
rs774203598 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102391148 | CACTCCATCCTGGGC[A/G]GCAGAGCAAGAACCT | 51366 |
rs774206242 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102272365 | CCGTAGAATAGCAAA[C/T]TGTTGTCCATTAGAA | 51366 |
rs774209560 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102267238 | GATAGTGGACTAAAG[G/T]CTCCCTGACAAAATG | 51366 |
rs774211305 | snp | C/G | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102313899 | CTTCTTTTGGTGCAG[C/G]GGTTGACCGTCGTCG | 51366 |
rs774214895 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102310580 | TCAAACTCCTGACTT[C/T]AAGTGATCCACCCCA | 51366 |
rs774240724 | snp | C/T | 1.6615e-05 | 0.00288223 | intron-variant | UBR5 | GRCh38.p7 | 8:102272784 | CAACCTATTAAAACA[C/T]ATCAAGAAGTCAAAA | 51366 |
rs774241764 | in-del | -/TTTTT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102396711 | ACATATATATATATA[-/TTTTT]TTTTTTCTTGAGACA | 51366 |
rs774248134 | snp | A/C | 1.65034e-05 | 0.00287253 | intron-variant | UBR5 | GRCh38.p7 | 8:102287382 | TCCACGCTGAATACA[A/C]ACACACAGCCTTAGC | 51366 |
rs774250790 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102307067 | AGAATCAAATGCCTA[C/T]ACTTGAAGTAATATA | 51366 |
rs774269944 | snp | C/G | 1.65455e-05 | 0.00287619 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295658 | TTGGCAGAGTAACCA[C/G]ATTAGTAGCAGTGAG | 51366 |
rs774295875 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102359586 | CCAGAAATAAATAAA[C/T]AGGATCAGGAACAAA | 51366 |
rs774300099 | snp | C/T | 5.07318e-05 | 0.0050362 | intron-variant | UBR5 | GRCh38.p7 | 8:102327720 | GCATTCACCGATAAA[C/T]TCCTCCTCCCTATAG | 51366 |
rs774323614 | snp | C/G | 1.65488e-05 | 0.00287647 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102346935 | CTGGAATGACAGATG[C/G]TGGAATAACTGGCTG | 51366 |
rs774330411 | snp | C/T | 1.6517e-05 | 0.00287372 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102261963 | TGCAAATGCCAAATC[C/T]ATTGCTGAGAAAACA | 51366 |
rs774331249 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102336444 | AAAAAAATCACTGCC[A/G]TGAGCAATGTCAAGG | 51366 |
rs774344079 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102382013 | TTTAATAGTGAGTCT[C/T]TGGTATAACAGTTTC | 51366 |
rs774351051 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102397411 | AAAGAATAAAAATCT[A/C]GCCTGGTGCGGTGGC | 51366 |
rs774351533 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102277383 | ACCTCAGATAACTAC[-/T]TTTTTTTTTTTTTTA | 51366 |
rs774394371 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102386022 | GATATGATTCTAATA[C/T]GATGTGCATAGTCCA | 51366 |
rs774403427 | snp | A/G/T | 1.6513e-05 | 0.00287336 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102286418 | CTGATGCTGGGTGTT[A/G/T]CGGACAGCCCACTGC | 51366 |
rs774407595 | snp | C/T | 3.33006e-05 | 0.00408034 | intron-variant | UBR5 | GRCh38.p7 | 8:102280495 | AAGTGAGTCATTTTA[C/T]TTGAAGTATTTGTAT | 51366 |
rs774411288 | snp | C/T | 0.000560399 | 0.0167298 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102272664 | GCTCATCCTTAAATG[C/T]GACTTTTACTCTGTG | 51366 |
rs774427683 | snp | A/G | 1.70761e-05 | 0.00292194 | intron-variant | UBR5 | GRCh38.p7 | 8:102261304 | GGCAATTTTGTCAAA[A/G]CAGTAAAACATTACT | 51366 |
rs774433575 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102260510 | ATTCCTCAAGACTCC[A/G]CCTAATGTTTGTTTC | 51366 |
rs774436924 | snp | C/T | 1.64855e-05 | 0.00287097 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102277147 | GGTTTTGCATGTTCA[C/T]TACATTTTTCAGATT | 51366 |
rs774437920 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102357207 | AAAAAATGTATCACT[G/T]GAGTTTAATCACGAG | 51366 |
rs774448286 | snp | A/G | 1.67804e-05 | 0.00289653 | intron-variant | UBR5 | GRCh38.p7 | 8:102326673 | ACACCCCTGAAAACA[A/G]AAAACATAAATTGGT | 51366 |
rs774451785 | snp | C/T | 1.65641e-05 | 0.00287781 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102293678 | CACTGCCCTGCATGG[C/T]ATCTATGCTAGTACT | 51366 |
rs774456294 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102398344 | TGCATTAAACTTAAA[C/T]CTAAGAGCTCAAAGT | 51366 |
rs774471369 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102367833 | CACAAATATATACAC[C/T]CCACTGGGGTTGGGG | 51366 |
rs774523748 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102332816 | CCCCACTGAATTCCT[C/T]GTAGAAAGGCCAATA | 51366 |
rs774526809 | snp | C/T | 1.65564e-05 | 0.00287714 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102361185 | AATAGTAGCCTGTTC[C/T]AATACATTCAAAGGG | 51366 |
rs774531253 | in-del | -/AAG | 1.80075e-05 | 0.00300057 | intron-variant | UBR5 | GRCh38.p7 | 8:102257720 | TCAGCATTTTCTCCT[-/AAG]AATGAAGAATGTAAA | 51366 |
rs774541225 | snp | C/T | 1.67178e-05 | 0.00289113 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102293811 | TGCTTGGAATACACG[C/T]TTGCATTTTCCAATT | 51366 |
rs774547833 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102363863 | GCTAAAAAATATTTA[A/C]ACTCAAGAACTCAAC | 51366 |
rs774567167 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102355551 | AATTTGATTTACAAA[A/G]TAACTTAATCACAAT | 51366 |
rs774575044 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102364028 | GGAAACAATGCCACC[C/G]AATAGCAAGAAATCC | 51366 |
rs774588176 | in-del | -/AC | | | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102414279 | CTGTTAATGAATTAC[-/AC]ACACACACACACACA | 51366 |
rs774598502 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102261484 | AAGGTGGGTGGATCA[C/T]GAGGTCAGGAGATCG | 51366 |
rs774598683 | in-del | -/CTG | | | intron-variant | UBR5 | GRCh38.p7 | 8:102266868 | GTTTCTTCAGAAATC[-/CTG]CTTTCATCCCCTTTA | 51366 |
rs774609405 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102345114 | ATGTCACTGTAAAGT[A/G]GAATTCTGCTTTTAG | 51366 |
rs774637699 | snp | C/G | 1.66131e-05 | 0.00288206 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285694 | TTGCTAGCTTCCAAA[C/G]CAGCTGCTGCAGCTG | 51366 |
rs774637772 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102308126 | CAACTTAAATTTCAC[C/G]TGTCTAAAACCAAAT | 51366 |
rs774696609 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102377314 | CTGTCTTTTCTCTTC[A/G]TCTAAAAATGGTTTC | 51366 |
rs774697868 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102335074 | AAAAAAGGATAATTA[C/T]TCAGCTTAAAAAAGG | 51366 |
rs774700827 | snp | C/T | 3.29685e-05 | 0.00405995 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102342624 | CTTCGTTCACGTAAA[C/T]GTAAAACGGATTCAC | 51366 |
rs774703931 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102296221 | AGGTACTTAAAATAA[C/G]GAAAACAAAAAATAC | 51366 |
rs774704097 | snp | G/T | 1.70072e-05 | 0.00291605 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102312153 | GGAATCTACATTCAC[G/T]GCTAATATTTCTGTT | 51366 |
rs774706935 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102373390 | CTAGCAGATAAGACC[A/G]AAAGACTTCTTCAGG | 51366 |
rs774713846 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102255471 | AAATCTGAAAAGAAA[C/T]AGAAAACAGGTACTC | 51366 |
rs774720658 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102295199 | AGGTTTTAATGAATA[C/T]GTACGGGTCTTTATT | 51366 |
rs774722036 | in-del | -/CT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102394546 | CATAGACTTTTTCAC[-/CT]CTTAGATAGAAAAAC | 51366 |
rs774724022 | in-del | -/AG | 1.8084e-05 | 0.00300694 | intron-variant | UBR5 | GRCh38.p7 | 8:102296994 | AATATCCTAAAATTA[-/AG]AGTGTACTTTTAAAG | 51366 |
rs774731551 | snp | A/G | 3.82804e-05 | 0.00437479 | synonymous-codon, intron-variant | UBR5 | GRCh38.p7 | 8:102361584 | TTAAAACTCTTACCT[A/G]TTTAAATTATATTTG | 51366 |
rs774753260 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102307058 | AGAGGTCACAGAATC[-/A]AATGCCTACACTTGA | 51366 |
rs774755234 | snp | C/G | 1.66302e-05 | 0.00288355 | intron-variant | UBR5 | GRCh38.p7 | 8:102312262 | TGCATGACACAAAAG[C/G]AATTTTGCTTTCAAA | 51366 |
rs774756931 | snp | C/T | 1.64906e-05 | 0.00287142 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311326 | GATGATAACAGCAGC[C/T]TTCTTTTTGATTGTT | 51366 |
rs774767590 | in-del | -/AA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102274242 | TTCTTTGTAAGAGAC[-/AA]AGAGTCTCTCACACT | 51366 |
rs774769031 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102268409 | CGGTTTCACCATGTT[C/G]GCTAGGCTGGTCTTG | 51366 |
rs774781181 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102261356 | AATTTTTAAATATAA[A/T]CACAATTATTTATTT | 51366 |
rs774799048 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102284785 | CTCACGCCTGTAATC[A/C]CAGCACTTTGGGAGG | 51366 |
rs774804084 | in-del | -/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102355038 | GAGGCTGAGGTGGGA[-/G]GAACACTTGAGGCTG | 51366 |
rs774809946 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102331223 | AGTCAAAGTTATGTG[C/G]ATTTTCAACTGCATG | 51366 |
rs774811561 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102331693 | CAATGCTCAATGTAC[G/T]TAATCAGTCCATCTT | 51366 |
rs774813926 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102367126 | GACAAGCACCTTTCT[A/G]AAAAGACAACCTATC | 51366 |
rs774825028 | snp | C/G | 2.10764e-05 | 0.00324619 | intron-variant | UBR5 | GRCh38.p7 | 8:102314858 | TACTTTCAGGCCTGA[C/G]ATAAGAAATAAGATT | 51366 |
rs774833224 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102349362 | ATCTCTACAAAAAAT[-/A]AAAAAAATTAGCCAG | 51366 |
rs774834741 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102405736 | AGGCAGCAGAATCGC[C/T]TGAACCCGGGAGGCG | 51366 |
rs774878238 | snp | C/G | 1.65468e-05 | 0.00287631 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102323353 | TCCATGTTTTTCAAG[C/G]TTTCAGGAGATCTAA | 51366 |
rs774882195 | snp | A/C | 3.40015e-05 | 0.00412305 | intron-variant | UBR5 | GRCh38.p7 | 8:102299991 | ATGAAATTAAATAAC[A/C]GCTCTTACCAGGATC | 51366 |
rs774884417 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102352565 | GGCTAAGCCTAACTA[A/T]TAATTTCACTCAAAA | 51366 |
rs774885968 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102282489 | CCTGGCCAACATGGC[A/G]AAACCCCGTCTCTAC | 51366 |
rs774906770 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102314358 | AAAATTCTATCCATG[A/G]TGTGGCAGTAAGTCT | 51366 |
rs774907357 | in-del | -/A | 1.6563e-05 | 0.00287771 | intron-variant | UBR5 | GRCh38.p7 | 8:102305318 | CAGACAAATTAGGGG[-/A]AAAAAACCTCAATGA | 51366 |
rs774916324 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102321714 | CTACAGTAACCAAAA[C/G]AGCATGGTACTGGTA | 51366 |
rs774920932 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102404692 | GGCAGGTGAACACCT[A/G]AGGTCGGGAGTTCGA | 51366 |
rs774933402 | in-del | -/TG | | | intron-variant | UBR5 | GRCh38.p7 | 8:102363433 | TTAAGGGTAATGTAT[-/TG]TGGAACCCATGAGCT | 51366 |
rs774945992 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102391440 | TTGTTAATTTCCTAT[A/G]AAGTGTGATAATGGT | 51366 |
rs774962417 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102403972 | AGGACCTAGCCTAGG[A/G]GGAAGTGACTGAAAA | 51366 |
rs774965684 | snp | A/G | 1.66255e-05 | 0.00288314 | intron-variant | UBR5 | GRCh38.p7 | 8:102269120 | ATGCCTGTAAATGAT[A/G]AACAAATGTTACTTG | 51366 |
rs774973150 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102365135 | ACACGTGGTTATGAT[A/G]AAAAACAATTTTAAG | 51366 |
rs774984008 | in-del | -/AC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102392481 | ACTAAAGCTACACAA[-/AC]ACACACACACACCTC | 51366 |
rs775000344 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102343466 | TAAATTGAACTATAC[-/A]AAATTACCATATATA | 51366 |
rs775007310 | snp | A/G | | | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102281350 | TTGCCTTAATCCAGT[A/G]TATAAGTGCTTGAAA | 51366 |
rs775007886 | snp | C/T | 1.64882e-05 | 0.00287121 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102277121 | CTGTTCTTCCCCTTC[C/T]TTTTTTTGCCGGTTT | 51366 |
rs775010050 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102312806 | ATTAAAGCAGCCTTC[A/G]GTCTGACAGAACTTT | 51366 |
rs775011343 | snp | C/T | 1.65715e-05 | 0.00287845 | intron-variant | UBR5 | GRCh38.p7 | 8:102295171 | CTAACGTAGGAAATA[C/T]ATAAATCTAAAAAGG | 51366 |
rs775012139 | snp | C/T | 1.76163e-05 | 0.0029678 | intron-variant | UBR5 | GRCh38.p7 | 8:102287607 | AGCACAAACTCACTA[C/T]GGTTTAAAACAGGGT | 51366 |
rs775018522 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102257401 | CTGGTATCTTCTGGG[A/T]CTAAGGACAGCATAT | 51366 |
rs775052160 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102402814 | CAGAGCCAATTTCTT[C/G]AAACGGCAGGTTCTC | 51366 |
rs775053425 | snp | C/T | 1.6498e-05 | 0.00287206 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102270087 | CTCTCCAAGTGCCTG[C/T]CGATGTGCTGGCAAA | 51366 |
rs775059832 | snp | A/C | 2.14922e-05 | 0.00327805 | intron-variant | UBR5 | GRCh38.p7 | 8:102257747 | TGTAAATAAAATATA[A/C]TATACCAGTTGTTGT | 51366 |
rs775064266 | snp | C/T | 1.66076e-05 | 0.00288158 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295284 | ACGCTCCAATGCAAG[C/T]TGGGCAAATCTTGGA | 51366 |
rs775073243 | snp | C/T | 1.64806e-05 | 0.00287054 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102342511 | CTTCTCCTAGAGATA[C/T]TGGACTTTGAACAGG | 51366 |
rs775075342 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102360697 | CAGAAAAAATTATCC[A/C]AGTAAAAATGTGTAT | 51366 |
rs775094334 | snp | A/G | 1.66576e-05 | 0.00288592 | intron-variant | UBR5 | GRCh38.p7 | 8:102329411 | CATCCTATAAAGTAA[A/G]ATACAATACTATAAA | 51366 |
rs775097468 | snp | C/G | 1.64849e-05 | 0.00287092 | intron-variant | UBR5 | GRCh38.p7 | 8:102267022 | CCTAAAAACAAAAAG[C/G]CTTTCACATTCCAGA | 51366 |
rs775129750 | in-del | -/TAT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102396709 | ACACATATATATATA[-/TAT]TTTTTTTTTTCTTGA | 51366 |
rs775132913 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102381642 | AAACCTACCTCCAAA[C/G]TGAGGAGTCACAGAT | 51366 |
rs775133294 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102362104 | TCTTGAACGGTCTTA[C/T]AGCACAAAATTGAAC | 51366 |
rs775153664 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102375061 | TTAAAATGTTTAAAC[A/G]TTTAAAAAGTAATTT | 51366 |
rs775166536 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102267374 | TCTCTAGCGAATTTA[A/G]TGATTCTAGAACACC | 51366 |
rs775170894 | snp | C/T | 6.65945e-05 | 0.00576999 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102254491 | ACTGGCTGGCAGTGA[C/T]GGGCTTGATGTCCAA | 51366 |
rs775171471 | snp | C/T | 3.76953e-05 | 0.00434122 | intron-variant | UBR5 | GRCh38.p7 | 8:102296853 | TATAAATCTAAACAG[C/T]TTATAATATTAAACT | 51366 |
rs775175570 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102294307 | TTGACATACAGTGAG[A/T]CCTAAATGTACGATT | 51366 |
rs775195625 | snp | C/G | 1.64925e-05 | 0.00287158 | intron-variant | UBR5 | GRCh38.p7 | 8:102287396 | ACACACACAGCCTTA[C/G]CATAAGCAAGAAAGT | 51366 |
rs775198446 | in-del | -/C | 1.68269e-05 | 0.00290055 | intron-variant | UBR5 | GRCh38.p7 | 8:102346200 | AGTCGAAAGAGCACT[-/C]CAGAAATGAGAAAAA | 51366 |
rs775211432 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102324584 | ATGTGGTAGATGACC[A/T]GAGGTACACACGAAG | 51366 |
rs775214090 | snp | C/T | 1.67891e-05 | 0.00289729 | intron-variant | UBR5 | GRCh38.p7 | 8:102280513 | GAAGTATTTGTATAA[C/T]ATGAACAGGAGCAAA | 51366 |
rs775270940 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102316931 | TCAACTGTTAATATA[C/T]AAATATGAGGGGGGA | 51366 |
rs775294131 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102337651 | TATATCTTTTTGATA[C/T]GTGTTGAATTCAGTT | 51366 |
rs775325918 | snp | C/T | 6.68472e-05 | 0.00578093 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102314753 | ACTTACTGTATGGCA[C/T]TGATGCACTGCTGGC | 51366 |
rs775329495 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102370448 | ATTCTTTTTAACTGA[C/T]AGATATATTTATGGG | 51366 |
rs775337476 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102369313 | CAGCAAGTGATTTCT[C/T]AAAGGTTGAGAGCAA | 51366 |
rs775357555 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102380189 | ACTTGAGGTCAGGAG[C/T]TCGAGACCAGCCTGA | 51366 |
rs775361769 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102255140 | TGATGCTCAGTAAAT[A/G]TGAACTTACACTTTT | 51366 |
rs775381993 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102308200 | ATTAAAATGTCTTCA[C/T]ATTCACTTCCTCTAT | 51366 |
rs775382394 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102351209 | TTCGAAAGAATTGAA[A/C]CCAGGGTCTTAAAGA | 51366 |
rs775392803 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102296386 | ATAATCCTAAAACAC[C/T]ACAGATGTTAGTGCT | 51366 |
rs775395035 | snp | A/G | 1.88663e-05 | 0.00307129 | intron-variant | UBR5 | GRCh38.p7 | 8:102327914 | AAAGAATAAAATATT[A/G]GAACTTTAAATAAAA | 51366 |
rs775395067 | in-del | -/AAAGAC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102266846 | ATTCATTTTATTTAT[-/AAAGAC]AGTTTCTTCAGAAAT | 51366 |
rs775435203 | in-del | -/TAAAA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102296213 | ACACCTTTAGGTACT[-/TAAAA]TAAGGAAAACAAAAA | 51366 |
rs775446454 | snp | A/G | 1.66863e-05 | 0.0028884 | intron-variant | UBR5 | GRCh38.p7 | 8:102311252 | TCAAGACTATTTAGT[A/G]GTGTTTTGTGAATTA | 51366 |
rs775450001 | snp | A/G | 3.32856e-05 | 0.00407942 | intron-variant | UBR5 | GRCh38.p7 | 8:102312284 | GCTTTCAAACTCCAT[A/G]ATAAACTCACGGAGT | 51366 |
rs775458893 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102288561 | AAAAATTAGCTGGGC[A/G]TGGTGCGTGCCTGTA | 51366 |
rs775469732 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102325949 | GAAGCTAATTCAGCC[C/T]GACACAAATATGTAA | 51366 |
rs775489592 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102409504 | TTTGCAGTACCATTC[C/T]GCCTGTCTAATCTTA | 51366 |
rs775495181 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102387182 | AAACCTCATGATTTA[C/T]CTAATCAGCCTCTAA | 51366 |
rs775506450 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102309251 | GTAGAGACAGGGTTT[C/T]GCTATGTTGCCCAGG | 51366 |
rs775510306 | snp | C/T | 1.66891e-05 | 0.00288864 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285736 | CTGATGGTACCACTC[C/T]GGCGTAAGTTTGAAG | 51366 |
rs775511133 | snp | A/G | 1.66551e-05 | 0.00288571 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102293841 | TGGCTGTGGAATAAA[A/G]TTGCTAGAACAAAAA | 51366 |
rs775519903 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102310123 | CTTATCCCATTTGTT[C/T]CCCCTCCTATATTTC | 51366 |
rs775576265 | in-del | -/TTT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102396713 | ATATATATATATATT[-/TTT]TTTTTTCTTGAGACA | 51366 |
rs775593687 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102411476 | CGCTTGAATCCATCC[C/T]CTCCCGGGGCAGGCA | 51366 |
rs775599139 | snp | C/T | 1.66123e-05 | 0.00288199 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102312190 | GGTATACAAAGCTTT[C/T]TAGGAGTCCTTTGGA | 51366 |
rs775599750 | in-del | -/A | 1.67323e-05 | 0.00289239 | intron-variant | UBR5 | GRCh38.p7 | 8:102269989 | CTTTAATTCAAAAGC[-/A]AAAAAAATAACACAG | 51366 |
rs775646698 | snp | A/G | 3.55025e-05 | 0.00421308 | intron-variant | UBR5 | GRCh38.p7 | 8:102262097 | ATCATATGAAACTCA[A/G]TTATGAAAGAAACAG | 51366 |
rs775667042 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102350293 | TGGAAAAAGAACAAA[A/G]TTGAAGGATTCACAC | 51366 |
rs775667851 | snp | A/C | 0.000129267 | 0.00803846 | intron-variant | UBR5 | GRCh38.p7 | 8:102286342 | GTATTCTTAGCAATA[A/C]TAAGTTTTCAGACTT | 51366 |
rs775701191 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102399435 | GCTCACCATCATGCC[C/T]GGCTTATTTTTGTAC | 51366 |
rs775720033 | snp | C/G | 1.66117e-05 | 0.00288194 | intron-variant | UBR5 | GRCh38.p7 | 8:102346232 | ATGACGGTGATCCAC[C/G]AACCTCCAGGCAAAT | 51366 |
rs775750151 | snp | A/C | 0.000108137 | 0.00735234 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102412165 | CGCCGACCCGCCAGC[A/C]CTATTACCTGTCATT | 51366 |
rs775750493 | snp | A/G | 3.44163e-05 | 0.00414813 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102271150 | TATCCCGGTCCCTCC[A/G]AGAACCTGCTCGCAA | 51366 |
rs775759826 | snp | A/C | 1.65433e-05 | 0.002876 | intron-variant | UBR5 | GRCh38.p7 | 8:102279021 | GAAACCTTAAGACTA[A/C]CTTGTTTAATTCACC | 51366 |
rs775809569 | in-del | -/AC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102372950 | AACGAAATGCTGAAC[-/AC]ACACACACACACACA | 51366 |
rs775823355 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102366321 | TGGTAGTTGTAATTT[C/T]CTTCCTACAGAAGTC | 51366 |
rs775837550 | snp | C/T | 1.65293e-05 | 0.00287479 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102323370 | TTCAGGAGATCTAAG[C/T]TGAAATCTACAGCTG | 51366 |
rs775842119 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102332977 | TACAATCCTGAACAA[A/T]CCAGCCCAATAGCAA | 51366 |
rs775846796 | snp | G/T | 1.64738e-05 | 0.00286995 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102289498 | CTGTTCTTCATCTCT[G/T]CCCCGAACGGGCTGT | 51366 |
rs775851259 | snp | A/G | 1.66774e-05 | 0.00288763 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102300011 | TTACCAGGATCCATC[A/G]CAGGAGGGTCAGGAA | 51366 |
rs775852673 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102409181 | GCCCAGCATTCTGTG[C/T]CAGGCACCTTGTAAT | 51366 |
rs775863293 | snp | C/T | 1.72216e-05 | 0.00293437 | intron-variant | UBR5 | GRCh38.p7 | 8:102285106 | GTTGGGGACGTTCTG[C/T]ATATATGAAGAATTT | 51366 |
rs775868826 | snp | A/G | 1.64906e-05 | 0.00287142 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102270109 | GCTGGCAAAGGCTCA[A/G]GATCATCGCTAGGAT | 51366 |
rs775872511 | in-del | -/T | 1.654e-05 | 0.00287571 | intron-variant | UBR5 | GRCh38.p7 | 8:102295611 | TTTGATTTAACTTAC[-/T]GTATGTTCTAAAAAT | 51366 |
rs775876834 | snp | A/G | 3.40397e-05 | 0.00412537 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102345520 | GGCAGAATGAATGTC[A/G]GCATCAAGGAGAGAC | 51366 |
rs775904638 | snp | A/T | 1.71938e-05 | 0.002932 | intron-variant | UBR5 | GRCh38.p7 | 8:102300190 | GAGCTCACTACCATA[A/T]CTACACATAATGAAA | 51366 |
rs775904703 | snp | A/C/G | 3.29692e-05 | 0.00406001 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295441 | CTGTTTTTCGGTTAC[A/C/G]ATCTTCCCTGATTCG | 51366 |
rs775908178 | snp | C/T | 1.68832e-05 | 0.00290539 | intron-variant | UBR5 | GRCh38.p7 | 8:102259164 | ATAATACTTCATTTT[C/T]CATGTAACATTTATT | 51366 |
rs775912072 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102339041 | AATGACCCTTACTTC[C/T]GTCTTTATGGAACTT | 51366 |
rs775925137 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102286722 | AAACAGAATGCCAGA[C/T]TGTATTCAATAATCC | 51366 |
rs775927922 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102353093 | CCGTACGTCAATCGC[C/T]ATTAACATTCCTCTA | 51366 |
rs775946882 | snp | A/T | 0.000181578 | 0.00952659 | intron-variant | UBR5 | GRCh38.p7 | 8:102254547 | AGGTTAATATTTAAC[A/T]CTTAACTCTGGCAGT | 51366 |
rs775961381 | snp | A/G | 3.31559e-05 | 0.00407147 | intron-variant | UBR5 | GRCh38.p7 | 8:102313947 | AATGGTAAGTACCAA[A/G]AAGAAAATGTAAAAG | 51366 |
rs775961441 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102314025 | GGGATACATAAGTGA[A/C]GTTTCTCAACAATTT | 51366 |
rs775962447 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102291659 | AGTCTGCATTTTGGA[A/G]AGTTTTGGACTGCAC | 51366 |
rs775962803 | snp | C/T | 9.88875e-05 | 0.00703093 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102288238 | TCATGATGATCCTCT[C/T]CTCCAGCCACACCCT | 51366 |
rs775965035 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102407312 | TTTTTGTATTTTTAG[G/T]AGAGATGGGGTTTCA | 51366 |
rs775966310 | snp | C/T | 0.000605999 | 0.0173963 | intron-variant | UBR5 | GRCh38.p7 | 8:102323545 | ATAACTTTAAAAATA[C/T]ATATAATATTTATTT | 51366 |
rs775966405 | in-del | -/ATCT | 4.34499e-05 | 0.0046608 | intron-variant | UBR5 | GRCh38.p7 | 8:102286317 | TGCATAATTTAAAAA[-/ATCT]ATCTAAGTATTCTTA | 51366 |
rs775971813 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102261517 | ACCATCCTGGCCAAC[A/G]TGGTGAAACCCCATC | 51366 |
rs776015186 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102330177 | CTACCTAGAAATCTC[A/G]CAGCAAAAATTGCCA | 51366 |
rs776019150 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102269690 | TAATGTGTTCCAACT[A/G]CAGCTTGCTAACAGA | 51366 |
rs776036742 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102321526 | GCCCAAGGTAATTTA[C/T]AGATTCAATGGTATC | 51366 |
rs776083050 | snp | C/T | 1.66043e-05 | 0.00288129 | intron-variant | UBR5 | GRCh38.p7 | 8:102288113 | CCCTTTAAAAGTACC[C/T]GATTTACTCATACTG | 51366 |
rs776097256 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102257863 | TTCCTAATACAAGAA[A/G]TTAAGAGCATTTGCA | 51366 |
rs776098422 | in-del | -/TTGA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102264408 | ACAGTATGCTAGCGT[-/TTGA]TTATTTTATAAAAGA | 51366 |
rs776104673 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102383348 | AACATTTCCTACTTA[G/T]CAAAATTCAGCCAGA | 51366 |
rs776110163 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102353397 | TACCTAGTATGGAAT[C/T]AGTCCACAGCTTGCA | 51366 |
rs776163298 | snp | C/T | 1.64806e-05 | 0.00287054 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102342612 | CCATCAAGCCACCTT[C/T]GTTCACGTAAACGTA | 51366 |
rs776172178 | in-del | -/AG | | | intron-variant | UBR5 | GRCh38.p7 | 8:102381298 | TTGAGCCCAGGAGGC[-/AG]AGTTTGCAATCAGCT | 51366 |
rs776183515 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102270647 | GCCTCAGCCTCCCAA[A/G]TAGCTGGGATTACAG | 51366 |
rs776215930 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102351278 | AATTGCCAAGTGGTA[G/T]AAGCTACCCAAATGT | 51366 |
rs776221732 | snp | A/G | 1.64866e-05 | 0.00287106 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102269078 | CTGGGGATAATTCCA[A/G]CAACATGCCAGTGAT | 51366 |
rs776224263 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102268269 | AGACGGGTTTCATCA[C/T]GTTGGTCAGGCTGGT | 51366 |
rs776229453 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102386846 | CCTGGTGTGGTGGCG[G/T]GCACCTGTAGTCCCA | 51366 |
rs776239524 | snp | A/C/G | 8.46391e-05 | 0.0065049 | intron-variant | UBR5 | GRCh38.p7 | 8:102275624 | TCAGTTAGGATCTTA[A/C/G]AAAAAAAAAAATGCA | 51366 |
rs776247397 | snp | A/C/T | 3.29496e-05 | 0.00405881 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102288231 | CTGTTCATCATGATG[A/C/T]TCCTCTTCTCCAGCC | 51366 |
rs776291618 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102325023 | TAATGCCATATTACC[A/T]GCTGATATGGCAGCT | 51366 |
rs776305850 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102363580 | GGTCCACATTTACTA[C/T]GAGTAACCACAGTAG | 51366 |
rs776307422 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102350353 | GAAGTATTTAAAACA[A/G]TATGGGTATGGGCAT | 51366 |
rs776312392 | snp | C/T | 1.65641e-05 | 0.00287781 | intron-variant | UBR5 | GRCh38.p7 | 8:102360023 | GCACTCACAGGAAGA[C/T]GATACAGACCATCTG | 51366 |
rs776314224 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102338625 | TCTCCTTGCTCTTTG[A/C]ACTTTACATAAACTA | 51366 |
rs776328466 | snp | C/T | 1.64779e-05 | 0.00287031 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102281357 | AATCCAGTATATAAG[C/T]GCTTGAAAAACATAT | 51366 |
rs776341066 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102385349 | TATTTCATACTTACT[A/G]TAAAAATAATGTGAA | 51366 |
rs776362153 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102360289 | ATGATCTATAAAATC[A/T]TTTCAGTTAAAGAGC | 51366 |
rs776375760 | in-del | -/ATTCTC | 1.7959e-05 | 0.00299652 | intron-variant | UBR5 | GRCh38.p7 | 8:102254522 | AGTAAACCTGAACAG[-/ATTCTC]GAATTTAACAGGTTA | 51366 |
rs776407733 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102371585 | ATTCTGGGTTGTTTG[G/T]TTTTTTTTTTTTTGA | 51366 |
rs776411830 | snp | C/G | 0.000358366 | 0.0133811 | intron-variant | UBR5 | GRCh38.p7 | 8:102327939 | ATAAAATCAAGCCAT[C/G]TTTTCAAAAGGATTG | 51366 |
rs776412815 | in-del | -/CTC | 3.29652e-05 | 0.00405974 | cds-indel, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102342499 | ACCACTGCAAATCTT[-/CTC]CTAGAGATACTGGAC | 51366 |
rs776418985 | snp | A/G | 1.64961e-05 | 0.00287189 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311320 | AGCCATGATGATAAC[A/G]GCAGCTTTCTTTTTG | 51366 |
rs776419006 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102406501 | GTTTCACCATGTTGG[C/T]CAGGCTGGTCTCAAA | 51366 |
rs776424812 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102264356 | TATTTATAATGGCTG[C/T]AATGCTTTAAGATTT | 51366 |
rs776425048 | in-del | -/CACCTAGCCTATG | 1.65897e-05 | 0.00288003 | frameshift-variant, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102312234 | TTCGGTGTTCCACCA[-/CACCTAGCCTATG]GTTTTGACAACCTGC | 51366 |
rs776426180 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102370498 | ACATGTACACAATGT[A/G]TATACATGTATACAA | 51366 |
rs776468125 | snp | C/T | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311427 | AATCGGGATCCCTTA[C/T]TCCTCCCATGCAATC | 51366 |
rs776470258 | snp | A/C | 1.67433e-05 | 0.00289333 | intron-variant | UBR5 | GRCh38.p7 | 8:102297412 | AGTCATAGCGAAAAA[A/C]GACACAAAGATATGA | 51366 |
rs776483129 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102357936 | GGATCACCTGAGGTC[C/T]GGAGTTCAAGACCAA | 51366 |
rs776487987 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102288650 | TGTAGTGAGGCAAGA[C/T]TGCACCACTGCATTC | 51366 |
rs776494094 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102296314 | TACGGTAGATGGTTT[C/T]TACAGTCCAATTCTC | 51366 |
rs776508904 | snp | A/C | | | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102286458 | GGAGCTTGGGCAGCA[A/C]CATTGGCATGGGAGC | 51366 |
rs776526575 | snp | G/T | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102286495 | TGGTTCTTTCTAATG[G/T]CTCATCAAGCATAAA | 51366 |
rs776532174 | snp | C/T | 1.64887e-05 | 0.00287125 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102329192 | TCGTGGATGATGTAA[C/T]GAAGGATTCTTTGAA | 51366 |
rs776534070 | snp | A/G/T | 8.36569e-05 | 0.00646705 | intron-variant | UBR5 | GRCh38.p7 | 8:102297643 | AGTTCATCTTTCAGG[A/G/T]AAGGACTTAATTAGC | 51366 |
rs776543862 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102272509 | AATTTTAAGCTGCTT[G/T]TTATTTGTAGAGTAC | 51366 |
rs776545865 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102298180 | TAAATCAATAAATTT[A/G]TATCAGCTGTTTTTT | 51366 |
rs776547683 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102399584 | GCCCAGCCTATATCT[A/C]ATCAATTTACAATCA | 51366 |
rs776550600 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102309351 | CAATCCACCATGCCC[A/G]ACTGTGTACAATGTG | 51366 |
rs776555747 | snp | A/C/G | | | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102413836 | GAGTTTTGGCCACGG[A/C/G]GCACAGTGGCTCACG | 51366 |
rs776575208 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102318821 | CTGTCAACTCAGAAT[G/T]TCATATCCAGCCAAA | 51366 |
rs776577657 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102377511 | AGGAGATTGAGGCCA[C/T]GCTGGCCAACATGGT | 51366 |
rs776587017 | snp | A/G | 1.64901e-05 | 0.00287137 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102312393 | CAGGAGAGAAGAAGG[A/G]TCAGCATCTGGACCA | 51366 |
rs776593439 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102339981 | TTCAGTCAAAATAAT[G/T]CAAGTTACCAAGATT | 51366 |
rs776596742 | snp | A/C/G/T | 6.6613e-05 | 0.00577088 | intron-variant | UBR5 | GRCh38.p7 | 8:102297624 | AAAAAAGTAAGAACA[A/C/G/T]AGCAGTTCATCTTTC | 51366 |
rs776598407 | snp | A/G | 1.65548e-05 | 0.002877 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102275801 | CATATCATGGGAAAT[A/G]ACCATTCCCATAAAG | 51366 |
rs776608246 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102284572 | TGAGGTCTTACATAA[C/T]AGCAACTAAAAAGCT | 51366 |
rs776649074 | snp | A/G | 1.65105e-05 | 0.00287315 | intron-variant | UBR5 | GRCh38.p7 | 8:102295553 | AAACAGAATGTTGTC[A/G]TGAGGAGGGAGGCTG | 51366 |
rs776650472 | in-del | -/GGA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102256562 | AAGAGCCATAAGACT[-/GGA]GAAGTCAAATGCTGA | 51366 |
rs776660254 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102388425 | GAATACACACAATAG[C/T]AGTATTTCAGTGCAG | 51366 |
rs776666576 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102344309 | TTAAGGATTTCAAAC[-/T]TTTTTTTTTTTTTTT | 51366 |
rs776669761 | snp | A/G | 1.65471e-05 | 0.00287633 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102300036 | CAGGAACCCAACTAG[A/G]GGGAGCTATGGGGGG | 51366 |
rs776670598 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102401117 | TGATTTTACTACAAT[C/T]TGACTAGGTTATGTT | 51366 |
rs776678441 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102263144 | TTAGCTGTAACTTTG[A/T]AATGACAAACAGCAG | 51366 |
rs776716814 | in-del | -/AT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102372984 | ACACACACACACACA[-/AT]CAGTCATGTTCCTTT | 51366 |
rs776753106 | in-del | -/A | 0.0100735 | 0.0702516 | intron-variant | UBR5 | GRCh38.p7 | 8:102285470 | TCATAATTGACAGCC[-/A]AAAAAAAATAGTGGA | 51366 |
rs776753935 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102276513 | TCTAATTCTCTCCAG[C/T]CTGTTTCTGCACATT | 51366 |
rs776756519 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102378202 | GAGCACAAATTAACA[C/T]AAATGATTCCTCTCT | 51366 |
rs776844943 | snp | A/G | 1.68698e-05 | 0.00290424 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102304190 | AAATGAGAAAAAATT[A/G]AGATCAATTTAAGTT | 51366 |
rs776854473 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102389447 | ATGAAGACACCCTCT[A/G]CATGACTCCAGCATT | 51366 |
rs776870063 | snp | A/G | 1.64909e-05 | 0.00287144 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102326599 | CAGCACTGGATTTAG[A/G]CTTTTTATTTTTTGC | 51366 |
rs776878527 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102272116 | GTAAAGTCCTTATCT[C/T]ACTGGGGACCAGGAG | 51366 |
rs776890685 | snp | C/T | 1.65658e-05 | 0.00287795 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102261238 | TGACTGGTATATTTA[C/T]ACCATTAGGAATGAG | 51366 |
rs776896549 | snp | A/C | 3.66213e-05 | 0.00427894 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102271233 | CCTCGGTTCCTTAAT[A/C]TCTGCATTAAACCTA | 51366 |
rs776910323 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102270719 | AGACAGAGTTTCACC[A/G]TGTTGGTCAGGCTGG | 51366 |
rs776913902 | snp | A/T | 1.71956e-05 | 0.00293215 | intron-variant | UBR5 | GRCh38.p7 | 8:102345569 | AGAAACAAACATCAC[A/T]GCAGCATACACACAA | 51366 |
rs776918802 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102340585 | TTTCCTAAAGTTACA[G/T]AAAAACAAGGTCTTC | 51366 |
rs776941294 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102409319 | AAAACACAAATTATG[-/A]AAAAAAAGATACTTT | 51366 |
rs776949107 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102366359 | TCTCTCATATCTAGT[A/C]ATTTGTGTTTCTATC | 51366 |
rs776961243 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102355275 | CAGGCCTAGACTCTG[C/T]AGGACAGGAGTGAGG | 51366 |
rs776966954 | snp | A/C | 1.64871e-05 | 0.00287111 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102346264 | AGATTCGCTGGCTGT[A/C]TCATCCCCATCATCT | 51366 |
rs776989562 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102379050 | CTTTTTTTTTTTTTT[-/A]AAAAATGCCTGGAAA | 51366 |
rs776996950 | snp | A/C | 1.66621e-05 | 0.00288631 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311885 | CTTCAGAACAGCATG[A/C]ACACCTTCAGAAGCA | 51366 |
rs776998609 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102353512 | GAGAAACGGTCACAG[A/T]CAAGAGGAATCTAAT | 51366 |
rs777007976 | snp | C/G | 3.29484e-05 | 0.00405871 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102289502 | TCTTCATCTCTGCCC[C/G]GAACGGGCTGTGACT | 51366 |
rs777015355 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102293192 | GGCCCCACCTCAAGA[C/T]CTCTAGAGTGGGCAT | 51366 |
rs777031294 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102411682 | ACCGGACACAGCTGC[C/G]GGGGGCCCGGGACAA | 51366 |
rs777056801 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102315841 | ATTTAAATTTCACTT[A/G]GCTCTTTTGCTAATA | 51366 |
rs777056931 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102335093 | GCTTAAAAAAGGAGA[A/T]CTTGCCATTTGCCAC | 51366 |
rs777081030 | snp | A/G | 1.66746e-05 | 0.00288739 | intron-variant | UBR5 | GRCh38.p7 | 8:102280376 | TGAAGTAGATTAGCA[A/G]ATTTTCTGTGCACTA | 51366 |
rs777099473 | snp | C/T | 0.00122044 | 0.0246725 | intron-variant | UBR5 | GRCh38.p7 | 8:102289607 | AGCTTATGAGTGGGC[C/T]CCTGCCACAGCTCAG | 51366 |
rs777117216 | in-del | -/AACT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102369010 | AATATTTTAAAAATA[-/AACT]AACTAAATATTGACA | 51366 |
rs777119297 | snp | C/T | 0.000569982 | 0.0168721 | intron-variant | UBR5 | GRCh38.p7 | 8:102298530 | AAATATTAATTACTA[C/T]TTATTTTCCTTCCTG | 51366 |
rs777162717 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102270539 | TTTTTTTTGCCAGAC[A/G]GAATTTTGCTCGTTT | 51366 |
rs777168612 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102366134 | ACTCTACAAGGTGAT[C/G]GTTTCCATATACTTG | 51366 |
rs777170131 | snp | A/G | 1.65403e-05 | 0.00287574 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102298926 | ATAAAATGAGCATTC[A/G]CCTTTCGATCCTTGG | 51366 |
rs777176437 | snp | C/G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102341786 | ACATACCATCAACAG[C/G/T]ATACATCAACTCTGT | 51366 |
rs777223622 | snp | A/G | 1.6736e-05 | 0.0028927 | intron-variant | UBR5 | GRCh38.p7 | 8:102346219 | AAATGAGAAAAACAT[A/G]ACGGTGATCCACCAA | 51366 |
rs777236870 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102373823 | TGCCGTTTTATTAAC[A/G]TCAAAGATGAAATCG | 51366 |
rs777238339 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102265822 | TTTACCAAATTTAGG[A/T]AGTGCCCAGCCATGA | 51366 |
rs777255551 | snp | A/G | 3.29794e-05 | 0.00406061 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102270117 | AGGCTCAGGATCATC[A/G]CTAGGATTCCCTTCA | 51366 |
rs777259254 | snp | A/G | 1.65619e-05 | 0.00287762 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285216 | AGCGTGAAGAGGATG[A/G]TTTGGATGTCCAGGA | 51366 |
rs777269850 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102367107 | GTACTATATAGATGG[C/T]AGAGACAAGCACCTT | 51366 |
rs777273947 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102272451 | ATGCACTCACACATA[C/T]AGAAACCATGATTAC | 51366 |
rs777276651 | snp | C/T | 1.75078e-05 | 0.00295864 | intron-variant | UBR5 | GRCh38.p7 | 8:102346869 | CCTCACCTTGTCCTG[C/T]TGTCTGACATTAAGT | 51366 |
rs777278637 | snp | A/C | 2.17082e-05 | 0.00329449 | intron-variant | UBR5 | GRCh38.p7 | 8:102323529 | CCACCATCAAGATGA[A/C]ATAACTTTAAAAATA | 51366 |
rs777282799 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102378992 | AGCTGCCTACCTTCC[A/G]GTCCCTAATTATCTT | 51366 |
rs777287430 | snp | C/T | 1.6693e-05 | 0.00288898 | intron-variant | UBR5 | GRCh38.p7 | 8:102311542 | CTCCTAATCAAAAAA[C/T]GTATCTGATTTTTAC | 51366 |
rs777308961 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102263799 | GCAATCATGCCTCAC[G/T]GAAGCCTCAAACTCC | 51366 |
rs777342166 | in-del | -/TAAA | 3.29832e-05 | 0.00406085 | intron-variant | UBR5 | GRCh38.p7 | 8:102264587 | CAGAGAAATAAGATT[-/TAAA]TAATTCTAGAATACA | 51366 |
rs777347856 | in-del | -/ATT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102355922 | AGGTTTTATTCAAAC[-/ATT]ATTATATTTGTTGTA | 51366 |
rs777355746 | snp | C/T | 4.99846e-05 | 0.00499898 | intron-variant | UBR5 | GRCh38.p7 | 8:102271122 | GTATTGAATCAAAGA[C/T]ACAAAATTTACCTAT | 51366 |
rs777399666 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102306661 | TACTTTCAAAGGGCA[A/C]CTAAAATCAAGATAT | 51366 |
rs777399776 | snp | A/G | 1.64923e-05 | 0.00287156 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102326564 | GGTACCAACAGTGAT[A/G]TTCGGCATTGAAGAA | 51366 |
rs777414891 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102408667 | AAAAGGTTAAGAGCG[C/T]CAGCCTCTGAAAAAA | 51366 |
rs777416156 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102305672 | CTTCATGTTATCTAT[C/T]TAATTAGAACCCTTT | 51366 |
rs777418254 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102316995 | TCTACAGCTCCCAGC[A/G]TCAGCTACTCAGAAG | 51366 |
rs777431352 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102407893 | TGACATTTTGGACCC[C/T]GTAATTCTTTGTTGT | 51366 |
rs777454572 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102385061 | CCTAGTACAAAATGT[G/T]AGCTGCTCCTGCTGT | 51366 |
rs777467994 | snp | C/G/T | 4.9549e-05 | 0.00497719 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285186 | CATCCTCTCTCTTCT[C/G/T]GCTGAATTCTGAGAA | 51366 |
rs777478448 | in-del | -/CTA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102350831 | ATATATAAATAACTC[-/CTA]CAACTCAACCAAAAA | 51366 |
rs777484389 | snp | A/G | 0.000217867 | 0.0104348 | intron-variant, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102276932 | ATATATATTTTTAAC[A/G]CTGTACTGAACAATA | 51366 |
rs777513864 | snp | C/T | 1.66579e-05 | 0.00288595 | intron-variant | UBR5 | GRCh38.p7 | 8:102298987 | CTGTAATTAAGCAGA[C/T]TCATTTGGTACAAAA | 51366 |
rs777526248 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102383871 | AAAATATCTCAGGGC[A/C]TGAGTTCATAAGGCA | 51366 |
rs777572603 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102277085 | TGGTTTTGAACTCTC[A/G]GTTTCTTCTGGCAGC | 51366 |
rs777606458 | snp | C/T | 1.6531e-05 | 0.00287493 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102261182 | TACCAACATTCTGTG[C/T]TCTGCGTATTTCCGC | 51366 |
rs777607827 | in-del | -/CTTA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102344994 | GGTCCTAAATCCATT[-/CTTA]CTAGTAAGTTTTTTC | 51366 |
rs777611559 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102280641 | AGGTTTAGGTACTAT[C/T]ATTACAAAATGGACT | 51366 |
rs777656422 | in-del | -/AC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102384850 | AAAACTCTAACCATA[-/AC]ACAATCAAGACCTAA | 51366 |
rs777657543 | in-del | -/T | | | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102414068 | CTGAGATCATGCCAC[-/T]TGCACTCCAGCCCGG | 51366 |
rs777663722 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102329533 | TATACGAAGTCTTTA[A/G]CACAGCCTACAAGGT | 51366 |
rs777665668 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102342697 | GAACTGGTATGCAAT[C/T]GGGTCACACCAGTGG | 51366 |
rs777671968 | snp | A/G | 3.29712e-05 | 0.00406011 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102360620 | GTTTACCCAATTCCA[A/G]TCTGTCTGGCTGTAC | 51366 |
rs777697810 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102392940 | AGATACTACAAAGAA[C/T]AGTAGTTCAATGGGC | 51366 |
rs777705926 | snp | C/T | 1.6486e-05 | 0.00287102 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102254422 | TGCAGTAGGAAGATG[C/T]TGGTCATCTGGTGGT | 51366 |
rs777714226 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102403518 | ATCACTACACTCCAG[A/C]CTGGGCAATAGCGCA | 51366 |
rs777725145 | snp | C/T | 0.000633492 | 0.0177861 | intron-variant | UBR5 | GRCh38.p7 | 8:102361088 | TCTATTTTAACAGTT[C/T]ATTTTTCATTTCTGT | 51366 |
rs777745378 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102392394 | GATAATTCATTGTTC[A/G]TTCTTTCAATTCTTC | 51366 |
rs777747987 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102361800 | AGATCACAAGCAGAC[C/T]CTGCAATTCCGTTCC | 51366 |
rs777753271 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102281985 | GATATCCTGGGCAAC[A/G]TGGTGAAACCCTGTC | 51366 |
rs777772572 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102350908 | GATATTTCTCCAAAC[A/G]TGATATATAAATGGC | 51366 |
rs777798544 | snp | A/G | 1.654e-05 | 0.00287571 | intron-variant | UBR5 | GRCh38.p7 | 8:102295132 | GGAGAAACGAAAGAC[A/G]GAATGAACTGTAAAA | 51366 |
rs777806674 | snp | A/G | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102342550 | TCTTATCCAAGTTTG[A/G]CTCTCCTTCCTTGCT | 51366 |
rs777836531 | in-del | -/AAAAA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102371276 | ATATCCTTTTTTTTT[-/AAAAA]AAAAAAAAAAAAAAA | 51366 |
rs777841744 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102267064 | TCTAGAATTTAGCGT[A/G]TAATTTAAATTTAAA | 51366 |
rs777854096 | snp | C/T | 2.2108e-05 | 0.00332468 | intron-variant | UBR5 | GRCh38.p7 | 8:102286648 | TTAAAACCAAAAACA[C/T]TGTGAGTTTAATAAT | 51366 |
rs777856300 | snp | C/T | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102305182 | TCTGTGGCTGATGAA[C/T]GTCTGCAGCATCTGT | 51366 |
rs777860813 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102349103 | GCATCCTCAAGGCTG[A/C]AGTATGAAACAGCAT | 51366 |
rs777861927 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102330650 | CTCTTCTCAATCCTA[C/T]GGTTAAGAATTAACT | 51366 |
rs777868437 | snp | A/T | 0.000315486 | 0.0125556 | utr-variant-3-prime, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102254252 | ACAAATGGAAAAAAA[A/T]CTACAAAATTTGCTA | 51366 |
rs777898331 | snp | A/G | 8.24831e-05 | 0.00642143 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102360076 | CACAACTTACCCTAA[A/G]GTGTTGCCTGCCAGC | 51366 |
rs777907826 | snp | G/T | 1.64784e-05 | 0.00287035 | intron-variant | UBR5 | GRCh38.p7 | 8:102268944 | TAAGTAGCTGATGTT[G/T]AAACTGAAATGCCTT | 51366 |
rs777908147 | snp | C/T | 6.59011e-05 | 0.00573988 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102305267 | GCCTCATAGTCACAG[C/T]GCAGAATGTGTTGCA | 51366 |
rs777910504 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102368759 | ATGCCCAGCCTAGGA[A/G]GGTTTTCTCTGAAAG | 51366 |
rs777914570 | snp | C/T | 3.29533e-05 | 0.00405901 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102281430 | TCAGAATGCTCATCA[C/T]TATGAGACCGCATTA | 51366 |
rs777918054 | snp | C/T | 1.66713e-05 | 0.0028871 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102257654 | TGTCGTTCTGTCATG[C/T]TCATCTTCTCTACTA | 51366 |
rs777918912 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102385928 | AATCTTACACAAAAC[C/T]ACAGACTAGTTAACT | 51366 |
rs777924950 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102337208 | TCTACATATAAGATC[A/G]TGTCATCTGCAAATA | 51366 |
rs777925716 | snp | A/G | 1.65831e-05 | 0.00287945 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295233 | CTGCGACCCAAACAT[A/G]ATCATAGATTTCAAG | 51366 |
rs777933932 | snp | A/C | 1.74573e-05 | 0.00295438 | intron-variant | UBR5 | GRCh38.p7 | 8:102314724 | TATTTTCACAAATGC[A/C]TACAACAAATAAAAC | 51366 |
rs777949834 | snp | A/G | 1.66313e-05 | 0.00288364 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102287555 | AACAAGTCCAGCTCC[A/G]TATCACTCCCTAAAA | 51366 |
rs777961658 | in-del | -/AG | | | intron-variant | UBR5 | GRCh38.p7 | 8:102408092 | ACTAATCTAGAACTA[-/AG]AGTCGATTCTGCTCT | 51366 |
rs777967254 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102273382 | TAAAACTATACTGAG[G/T]TGCTATTTCTTACCT | 51366 |
rs777998977 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102380085 | GAAAACTAACCATCT[A/G]ACAGAAGAGGAAAAA | 51366 |
rs777999157 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102256870 | TCCCCTTATTCAAAT[-/A]AAAATAAAGGATATA | 51366 |
rs778017046 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102288461 | AACACTCTGGGAGGC[C/T]GAGACGGAGATGGGC | 51366 |
rs778024164 | snp | C/T | 1.65288e-05 | 0.00287474 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102281299 | GATACCTTTTGCGTT[C/T]TAGTTGAGGTGTATC | 51366 |
rs778025110 | snp | C/T | | | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295670 | CCAGATTAGTAGCAG[C/T]GAGCAGGCGATAAAG | 51366 |
rs778030109 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102383633 | GCTATGAAGTTGTCA[G/T]ACATCCAACCACCAG | 51366 |
rs778035003 | in-del | -/G | 1.66679e-05 | 0.00288681 | intron-variant | UBR5 | GRCh38.p7 | 8:102280497 | TGAGTCATTTTACTT[-/G]GAAGTATTTGTATAA | 51366 |
rs778080963 | in-del | -/A | 3.31452e-05 | 0.00407081 | intron-variant | UBR5 | GRCh38.p7 | 8:102361108 | TCATTTCTGTATCTT[-/A]AGAGTGAATAATTTA | 51366 |
rs778084168 | snp | A/C/T | 3.30569e-05 | 0.00406541 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102297551 | AGGGTTGGTACCTGA[A/C/T]GGGCAAACCATTCCC | 51366 |
rs778104946 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102399201 | GATCCTGCTTACTCC[A/G]ACTTACATTCTATCT | 51366 |
rs778110460 | snp | C/G | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102288194 | GTCCCTCTGCCTCAG[C/G]ATTTTCTTCCCCGTG | 51366 |
rs778111773 | snp | A/G | 1.64898e-05 | 0.00287135 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102272718 | ATCTTCGACCAAAGT[A/G]ATTGTTAAGCTGCCT | 51366 |
rs778115686 | snp | A/C/T | 8.28897e-05 | 0.0064373 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285677 | TTAGGTAACTGCTGG[A/C/T]GTTGCTAGCTTCCAA | 51366 |
rs778128984 | snp | C/T | 1.65438e-05 | 0.00287605 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102347063 | GAGGATCCTCCACCA[C/T]TTCCACCCACTCCAG | 51366 |
rs778129293 | snp | A/G/T | 0.000173981 | 0.00932536 | intron-variant | UBR5 | GRCh38.p7 | 8:102262083 | GACCTAAAAAAGTAA[A/G/T]CATATGAAACTCAGT | 51366 |
rs778133338 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102355657 | TAAACATCTGCAAAC[C/T]CAAATATAAGTAAAC | 51366 |
rs778156976 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102262556 | AAACCCTGCTGAAGA[C/T]TCAATATATCAACAA | 51366 |
rs778160886 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102326727 | CTAAATAAATCTGAA[A/C]TTACACATATTATCA | 51366 |
rs778186225 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102358797 | TTTTTTTGAGACGGG[A/G]GTCTCTCATTTCCAT | 51366 |
rs778194257 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102381039 | GCTGGAGAGAGAAAG[C/G]AAACGAGAACAGGGA | 51366 |
rs778194281 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102391439 | TTTGTTAATTTCCTA[C/T]AAAGTGTGATAATGG | 51366 |
rs778218399 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102305064 | TCCCTTTAAAGACCT[C/T]GCTATAGTTCTTAAT | 51366 |
rs778229690 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102332480 | TGGCAAACTGTCTAG[C/T]CATCTCCATCCCATC | 51366 |
rs778247381 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102307822 | ACTTCCAGGACACAA[C/T]TCATTCTAGCTTTCC | 51366 |
rs778273647 | snp | A/G | 9.96545e-05 | 0.00705814 | intron-variant | UBR5 | GRCh38.p7 | 8:102312250 | GTTTTGACAACCTGC[A/G]TGACACAAAAGGAAT | 51366 |
rs778296997 | snp | C/G | 9.98627e-05 | 0.00706551 | missense, nc-transcript-variant, intron-variant | UBR5 | GRCh38.p7 | 8:102264482 | CACTTACTTTTCTAC[C/G]AAGCAATACTTTAAT | 51366 |
rs778297911 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102273807 | AAGATGGAATAAAAT[A/G]TATAGTATGTTTGGG | 51366 |
rs778299762 | snp | A/G | 3.5014e-05 | 0.00418399 | intron-variant | UBR5 | GRCh38.p7 | 8:102261900 | CAGAATCAGAAAAGT[A/G]TATATTTGCTTTACC | 51366 |
rs778304413 | snp | A/G | 1.64857e-05 | 0.00287099 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102327821 | TCCGCTCTCCTTGAA[A/G]TTCAGAGTAAGTCTG | 51366 |
rs778310793 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102334847 | AGCTTGCAAGGAGCC[A/G]AGATCGTGCCACTGC | 51366 |
rs778311892 | snp | A/C | 0.000171309 | 0.00925339 | intron-variant | UBR5 | GRCh38.p7 | 8:102326710 | AGCAGTAAAACAGCC[A/C]ACTAAATAAATCTGA | 51366 |
rs778315713 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102354128 | ATGTGACTGTGTGTA[A/T]GTGTATATTTATTTC | 51366 |
rs778316834 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102370313 | CTGAGATTACAAGCA[C/T]ACGCCACCACGCCTG | 51366 |
rs778318565 | snp | C/T | 3.31549e-05 | 0.0040714 | intron-variant | UBR5 | GRCh38.p7 | 8:102293949 | AAATCAAAAAGGATG[C/T]CTTACTTTTTCTTTT | 51366 |
rs778333642 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102354994 | TTAGCAGGGTGTGGT[A/G]GGGCATGCCTGTAGT | 51366 |
rs778357447 | in-del | -/AAA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102399946 | GCAAGACTCTGTCTC[-/AAA]AAAAAAAAAAAAAAA | 51366 |
rs778373471 | in-del | -/A | 0.148243 | 0.228354 | intron-variant | UBR5 | GRCh38.p7 | 8:102329212 | ATTCTTTGAAAGCAT[-/A]AAAAAAAAATTACTA | 51366 |
rs778398367 | snp | C/T | 5.18139e-05 | 0.00508962 | intron-variant | UBR5 | GRCh38.p7 | 8:102299962 | CATGACCTGCTCTTT[C/T]TGTTAAACACTAAAT | 51366 |
rs778399551 | snp | A/G | 1.68843e-05 | 0.00290549 | intron-variant | UBR5 | GRCh38.p7 | 8:102285380 | AAACTATCCAAATAG[A/G]GCTAAATTCGATACA | 51366 |
rs778404570 | in-del | -/TTT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102326898 | AAATTCATCAATTGC[-/TTT]TTTTTTTTTTTTTTT | 51366 |
rs778410384 | snp | A/T | 0.000109346 | 0.0073933 | intron-variant | UBR5 | GRCh38.p7 | 8:102286312 | GAACATGCATAATTT[A/T]AAAAATCTATCTAAG | 51366 |
rs778412241 | in-del | -/ATC | | | utr-variant-3-prime, downstream-variant-500B, cds-indel | UBR5 | GRCh38.p7 | 8:102253718 | CAAAATATTAGTGAT[-/ATC]ATTTAATATCCTAGA | 51366 |
rs778419394 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102332342 | CCATCATGCCAGTAA[C/T]GTTCACCTCCTTAAA | 51366 |
rs778419766 | snp | C/T | 6.606e-05 | 0.00574679 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311853 | TCAAAGATACAGTAT[C/T]GTACCCAATTTCCAG | 51366 |
rs778421157 | snp | C/T | 1.64784e-05 | 0.00287035 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102329107 | TGTTATTTTCTGTAG[C/T]TACAGTTGCTCTTAT | 51366 |
rs778423182 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102296997 | ATCCTAAAATTAAGA[A/G]TGTACTTTTAAAGGA | 51366 |
rs778442699 | in-del | -/CATA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102396665 | ACACACACACACACA[-/CATA]TATATATATATACAC | 51366 |
rs778472849 | snp | A/G | 2.23901e-05 | 0.00334583 | intron-variant | UBR5 | GRCh38.p7 | 8:102312087 | ATTTCCTGAACAAGT[A/G]TTAATGGAATATAGG | 51366 |
rs778519133 | snp | C/T | 1.6582e-05 | 0.00287936 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102293613 | AATTTACCTGCTAGA[C/T]TGATCAGATGATGGT | 51366 |
rs778519286 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102260782 | ATCTGACCAGAAGCT[A/C]AGTGATGGAAACATT | 51366 |
rs778528466 | in-del | -/AAC | 1.65866e-05 | 0.00287976 | intron-variant | UBR5 | GRCh38.p7 | 8:102329042 | AAAAGAAAAAAAGAA[-/AAC]AAGAATTAAAGCATG | 51366 |
rs778528473 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102332127 | GGTAATGGGAGACAC[A/G]ACAATCGAATTGACT | 51366 |
rs778546636 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102392029 | AGTTACCCTATATGG[G/T]CTAAAAAGGGGAGGA | 51366 |
rs778558403 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102294699 | ACTAGTATTAGGCTG[A/C]TATTTTTCTGTTTTT | 51366 |
rs778564052 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102397593 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 51366 |
rs778572205 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102259931 | TACTCAGGAGGCTGA[C/G]ACAGGAGAATCACTT | 51366 |
rs778594017 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102375725 | TACAGGGACCAAAAG[G/T]AAGCTGGAAGCAATA | 51366 |
rs778615884 | snp | C/T | 1.64784e-05 | 0.00287035 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102266971 | TTCTGAGGAGTCTAC[C/T]AATCCAAGATCCAGG | 51366 |
rs778628997 | in-del | -/TA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102409983 | CCTACGGCACCTTTC[-/TA]TTTTTCAAATATCTG | 51366 |
rs778645697 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102307512 | AGTCTATTTTAGATG[C/T]AGTTCTAAAAAGTAC | 51366 |
rs778646381 | snp | A/G | 1.69622e-05 | 0.00291219 | intron-variant | UBR5 | GRCh38.p7 | 8:102299561 | ATCTTTCAGTAAACA[A/G]AACAGTAGGATGTAT | 51366 |
rs778650672 | snp | A/G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102405428 | ATTCATAACCACAGT[A/G/T]AGCCAAGAGAAGAGG | 51366 |
rs778664006 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102374987 | ACATTCATGTCTTAG[C/T]TCTAAGCCCTACACT | 51366 |
rs778665512 | snp | C/T | 3.30218e-05 | 0.00406323 | intron-variant | UBR5 | GRCh38.p7 | 8:102295375 | CAAAAATAAAACATA[C/T]TGCTTCCCACAAGTG | 51366 |
rs778686407 | snp | G/T | 1.70615e-05 | 0.00292069 | intron-variant | UBR5 | GRCh38.p7 | 8:102299410 | AAAGTGTGTCCTTTT[G/T]TCTTCCAGATGACTA | 51366 |
rs778689597 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102403774 | ACCTCCACCTTCCCA[A/G]GTCAAGCAATGAAAA | 51366 |
rs778694192 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102254880 | CCAAACAAAAGATAC[A/G]GTCTTAGGTTCAAAA | 51366 |
rs778702782 | snp | A/G | 3.33261e-05 | 0.0040819 | intron-variant | UBR5 | GRCh38.p7 | 8:102277199 | TGGAAGAACCTATGA[A/G]TATTTACATTTAAAA | 51366 |
rs778703660 | snp | A/T | 3.29511e-05 | 0.00405887 | intron-variant | UBR5 | GRCh38.p7 | 8:102268964 | TGAAATGCCTTCCCA[A/T]TTGTACACATTACCG | 51366 |
rs778718705 | snp | C/G | | | | | GRCh38.p7 | 8:102260317 | ATGGCTGGTTGTGCA[C/G]ATAGAAAATGCCCAT | 51366 |
rs778746283 | snp | A/G | | | | | GRCh38.p7 | 8:102386221 | GATCACCTGAGGTCA[A/G]GAGCTTGAGACCAGC | 51366 |
rs778756459 | in-del | -/GATA | | | | | GRCh38.p7 | 8:102370446 | ATATTCTTTTTAACT[-/GATA]GATATATTTATGGGG | 51366 |
rs778765371 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102399010 | TATAAATGGCAAACA[C/G]GTATATGATGAAAAA | 51366 |
rs778765665 | snp | A/G | 6.62712e-05 | 0.00575597 | intron-variant | UBR5 | GRCh38.p7 | 8:102305318 | CAGACAAATTAGGGG[A/G]AAAAAACCTCAATGA | 51366 |
rs778780028 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102323895 | CTTAAACCTGGGAGG[C/T]GGAGGTTGCAGTGAG | 51366 |
rs778783853 | snp | C/T | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102288210 | ATTTTCTTCCCCGTG[C/T]TCTTCCTGTTCATCA | 51366 |
rs778793640 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102337512 | CAAATGCTTTTTCTG[C/T]GTCAATCAAGGTGTT | 51366 |
rs778807579 | snp | A/C | 1.785e-05 | 0.00298742 | intron-variant | UBR5 | GRCh38.p7 | 8:102361220 | GGCTGAGAGATAAAA[A/C]AAGAAAAAGTTAAAT | 51366 |
rs778813446 | snp | A/G | 1.66203e-05 | 0.00288268 | intron-variant | UBR5 | GRCh38.p7 | 8:102342449 | TCCATTTAAATGGAA[A/G]CAGTGTGAATTTTTT | 51366 |
rs778813501 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102312720 | CAGTGATTACAGTCA[A/G]TGAATGTTTTCAGTA | 51366 |
rs778822091 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102402890 | AAATAAAAACTTATC[C/T]ACTGATCCATTCATC | 51366 |
rs778824735 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102413087 | ATTCCCCTGGGGCAG[C/T]CCTAATTATTTGGCG | 51366 |
rs778828284 | in-del | -/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102288476 | GAGACGGAGATGGGC[-/G]GGATCACAAGGTCAA | 51366 |
rs778833418 | in-del | -/TT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102380722 | AAATTTAACATGCTT[-/TT]TTTTTTTTTTTTTTT | 51366 |
rs778851439 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102382634 | GTAAGGCTTGAGTGC[A/G]CTTTGATAAGTTAGT | 51366 |
rs778859319 | snp | A/G | 1.66313e-05 | 0.00288364 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102257677 | CTCTACTATTGACCA[A/G]AACCAACGCTTGAAC | 51366 |
rs778864299 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102393053 | TTCAAAAGTGTTTCA[C/T]GCAACATCTTGTCAC | 51366 |
rs778865832 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102393781 | CTAAAAACACAAAAA[C/T]TAGCCGAGCATGGTG | 51366 |
rs778877300 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102350991 | ACCAAACTACAACAA[A/G]AGATTAACTAATGCT | 51366 |
rs778880921 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102345139 | TTTTAGTTCAGAATC[C/T]ATATTCCTAATTAAA | 51366 |
rs778881297 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102372031 | ATGATCGCCCCACTG[A/C]ACTCCAGCCTGGACA | 51366 |
rs778890738 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102268777 | TAACCTTGGTAACTA[C/T]TAAAACCCTACCTTT | 51366 |
rs778908018 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102405812 | TCCAGCGTGGGCAAG[A/G]GCGAGACTCAAAAAA | 51366 |
rs778918467 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102338260 | GAAACCAGTATCAAC[C/T]TGGCTGGTTTCACTG | 51366 |
rs778934415 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102347707 | GCAGTAGCACGATCT[C/T]GGCTCACTGCAACCT | 51366 |
rs778949185 | snp | A/C | 1.86995e-05 | 0.00305767 | intron-variant, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102258938 | GAAAATGCTGACTGA[A/C]CTATCTATATAGTTC | 51366 |
rs778949507 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102399260 | AAATCACTACATAAT[A/G]TATATTATCTCATCA | 51366 |
rs778973014 | snp | A/C | 1.7294e-05 | 0.00294053 | intron-variant | UBR5 | GRCh38.p7 | 8:102287596 | AATAAGAAAAAAGCA[A/C]AAACTCACTATGGTT | 51366 |
rs778988405 | snp | C/G/T | 3.29828e-05 | 0.00406085 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102360190 | GCTGTTCAACTTTGA[C/G/T]CTGGGGGAAAGCAAG | 51366 |
rs778989430 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303102 | GAAATACCTGAAATA[A/G]TTCAGACACTAATTT | 51366 |
rs778990627 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102276181 | TGAACCAGAATCTCC[A/C]TTTGTTAAATAAATA | 51366 |
rs779003930 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102313499 | GAGATCCAACAAATG[A/G]GCTGTACCAAAAAGT | 51366 |
rs779010228 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102385534 | AATTTCTTGACTCTG[-/T]TTTTTTTTTTTTTTT | 51366 |
rs779013849 | in-del | -/A | 8.30806e-05 | 0.00644464 | intron-variant | UBR5 | GRCh38.p7 | 8:102293932 | AATGGTATCTAAACC[-/A]AAAATCAAAAAGGAT | 51366 |
rs779024718 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102287166 | AATGAGACCCAATTT[-/A]AAAAAAAAAAAAAAA | 51366 |
rs779045578 | snp | C/T | 3.29538e-05 | 0.00405904 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102329135 | TATGCTATTTGCAGA[C/T]AGGAGGACTATCTTT | 51366 |
rs779049405 | snp | C/T | 1.65312e-05 | 0.00287495 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102297566 | TGGGCAAACCATTCC[C/T]ATGAATACATCTTCC | 51366 |
rs779054300 | snp | A/C/T | 1.64838e-05 | 0.00287083 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102360110 | CCTAGAGTCTCAGAA[A/C/T]CTGAGAGAAACCATG | 51366 |
rs779058564 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102381194 | AACATGGTGAAACCC[C/T]GTTTCTATGAAAAAT | 51366 |
rs779072887 | snp | A/C | | | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102289566 | TGTAGGATGACTGAG[A/C]CTGACTGGAGCTGTA | 51366 |
rs779082868 | snp | C/T | 3.29473e-05 | 0.00405864 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102311394 | TTCCAAGACTACTAA[C/T]AGGTGGAAGATCCAG | 51366 |
rs779085072 | snp | C/T | 1.65416e-05 | 0.00287586 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102275566 | TCTCAGTTTTTCCAT[C/T]TCTCTGCGGAATTTT | 51366 |
rs779096771 | snp | A/G | 2.1564e-05 | 0.00328353 | intron-variant | UBR5 | GRCh38.p7 | 8:102286321 | TAATTTAAAAAATCT[A/G]TCTAAGTATTCTTAG | 51366 |
rs779110731 | snp | A/G | 1.65436e-05 | 0.00287602 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102293967 | TACTTTTTCTTTTTG[A/G]ATGAAGCCATTTCCA | 51366 |
rs779148037 | snp | C/G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102274397 | AATGTTGTTGGGAAG[C/G/T]TGGCTATTCAGTTTG | 51366 |
rs779159745 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102297782 | CAACTCTGGAACAAT[-/A]ATAAAGTAAAGCATA | 51366 |
rs779165250 | snp | A/G | 3.41682e-05 | 0.00413315 | intron-variant | UBR5 | GRCh38.p7 | 8:102281557 | GTTTATTAGAAGAAT[A/G]CAAATGTGAAATTCA | 51366 |
rs779180201 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102361470 | GATTAAAAGATTCTT[-/A]AAAGTCTAATAATCA | 51366 |
rs779184157 | snp | C/T | 1.65037e-05 | 0.00287256 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102327846 | AGTCTGAGCAGTGTG[C/T]TCTAATTTAGAAGCC | 51366 |
rs779200542 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102399945 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 51366 |
rs779200705 | snp | C/T | 6.72212e-05 | 0.00579708 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102294097 | CTTTCACTAGTGTAC[C/T]TAGTAGAGTATCTAA | 51366 |
rs779203112 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102264913 | ACAGGGTTTCGCCAT[A/G]TTGCCCAGGCAGGTC | 51366 |
rs779214762 | in-del | -/TTAGATCTTTTAAAAC | 1.65537e-05 | 0.0028769 | intron-variant | UBR5 | GRCh38.p7 | 8:102360688 | AAAGAAAACAGAAAA[-/TTAGATCTTTTAAAAC]AATTATCCAAGTAAA | 51366 |
rs779247467 | snp | C/T | 1.74766e-05 | 0.00295601 | intron-variant | UBR5 | GRCh38.p7 | 8:102262086 | CTAAAAAAGTAATCA[C/T]ATGAAACTCAGTTAT | 51366 |
rs779254568 | snp | A/T | 1.6569e-05 | 0.00287824 | intron-variant | UBR5 | GRCh38.p7 | 8:102278981 | TTACATTGAATACTT[A/T]AAAGAAAATAAACCC | 51366 |
rs779265597 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | UBR5, LOC105375683 | GRCh38.p7 | 8:102412889 | GCTGTAAGGCGCGTG[C/T]CGATTGGTCCGTTCG | 51366 |
rs779330736 | snp | A/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102275737 | CTCCAACATCTTCCA[A/T]GAATACCCTGCCGAA | 51366 |
rs779351879 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102400622 | CAGTCTTTCATAGTG[C/T]TACTATCTATGGATG | 51366 |
rs779352664 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102347415 | GGGGATTATAGGCAC[A/G]CACTACCATACCTGA | 51366 |
rs779359141 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102359121 | ATTTGTGGTCTGGAG[A/G]GAAAAAAGCCAAACA | 51366 |
rs779430955 | snp | A/G | 2.36309e-05 | 0.00343728 | intron-variant | UBR5 | GRCh38.p7 | 8:102361536 | GAGTTTTTTCTTAAT[A/G]AAGAAAAATTGTTGT | 51366 |
rs779433501 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102377886 | TCCAATATAAGCAGA[A/C]CCTGCTGGGCATCTT | 51366 |
rs779442371 | snp | C/T | 1.65781e-05 | 0.00287902 | intron-variant | UBR5 | GRCh38.p7 | 8:102312335 | TGAATAACTTCTTTA[C/T]ACTTACCTGCAATTC | 51366 |
rs779443239 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102386392 | TCGATCACAGCACTG[C/T]ACTCCAGCCAGGGCG | 51366 |
rs779446541 | snp | A/G | 1.6476e-05 | 0.00287014 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102286457 | GGGAGCTTGGGCAGC[A/G]CCATTGGCATGGGAG | 51366 |
rs779459673 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102393952 | AACAATAAAAAGTTT[C/G]TAGAGGAAAAAATAT | 51366 |
rs779497098 | snp | A/C/T | 0.000221979 | 0.0105329 | intron-variant | UBR5 | GRCh38.p7 | 8:102300183 | AAAATCAGAGCTCAC[A/C/T]ACCATATCTACACAT | 51366 |
rs779499557 | snp | C/T | 1.67251e-05 | 0.00289176 | intron-variant | UBR5 | GRCh38.p7 | 8:102312495 | TAGCACCTGGAAGTA[C/T]AGGCAAATTCAATGA | 51366 |
rs779517987 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102406955 | CTATGCCAACACTAT[A/C]CAAGAGAACTTTCAG | 51366 |
rs779534667 | snp | A/T | 4.9788e-05 | 0.00498914 | splice-acceptor-variant | UBR5 | GRCh38.p7 | 8:102279210 | ATTCAAAGTAGCACC[A/T]AAACATAAAAAGATA | 51366 |
rs779538949 | in-del | -/AGG | | | intron-variant | UBR5 | GRCh38.p7 | 8:102321099 | CCAGGGCAATTAGGC[-/AGG]AGAAGTAAATAAAGG | 51366 |
rs779544634 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102333856 | TCTCTCTGCCTATCC[A/G]CTTTTCCATATGCTT | 51366 |
rs779557656 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102333440 | ATTTTTCAACAAAAA[C/G]AAGTTGAATCAGTAA | 51366 |
rs779561521 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102372431 | TGGCTTCTTGAATCA[C/T]AGTTTGTAAGGAGGA | 51366 |
rs779563810 | snp | A/G | 3.29565e-05 | 0.00405921 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102342593 | TTCATTATCAAATGA[A/G]GCTCCATCAAGCCAC | 51366 |
rs779585023 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102297917 | TTAGCAAATTATAGA[C/T]CATCTCATAAACTAT | 51366 |
rs779586678 | in-del | -/GAT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102402330 | GGGTTTGTAGAGGCA[-/GAT]GATGTTACAGAGCAA | 51366 |
rs779612222 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102387574 | ACAAAAATTAGCCAG[A/G]CGTGGTAGCATGCAC | 51366 |
rs779617744 | snp | C/T | 6.59544e-05 | 0.0057422 | intron-variant | UBR5 | GRCh38.p7 | 8:102288273 | CACCTCAACCTAAAT[C/T]CAGAATCTTATTTGT | 51366 |
rs779619645 | snp | A/G | 5.13993e-05 | 0.00506922 | intron-variant | UBR5 | GRCh38.p7 | 8:102299577 | AACAGTAGGATGTAT[A/G]TCATTATAGGCAACA | 51366 |
rs779622090 | snp | A/G | 1.65605e-05 | 0.0028775 | missense, upstream-variant-2KB, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102304142 | GAAAGCCTTTCTGCA[A/G]ATGTATTTCTTTCAG | 51366 |
rs779623000 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102268983 | TACACATTACCGTCC[A/G]TGTGCAATAATGAGT | 51366 |
rs779648966 | in-del | -/TATT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102254976 | ATAAAGCAAAAAAAG[-/TATT]TACTGCTACATTGTG | 51366 |
rs779657098 | snp | A/G | 6.61081e-05 | 0.00574888 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102285610 | AGGCCCATCAAGTCC[A/G]AGATTTGTCTAATGA | 51366 |
rs779672509 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102256357 | TAGATTAAAATAGAT[G/T]ACTTAGAACTTATAC | 51366 |
rs779673194 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102283202 | GATGTATGCTAAATA[C/T]AGATGAACCTGAAAA | 51366 |
rs779704520 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102375948 | ACCTAATGCTTACCA[A/G]AATAGGAATAATTGG | 51366 |
rs779718879 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102405565 | GTGGCTCCCGCCTGT[A/G]ATCCCAACACTTTGG | 51366 |
rs779726085 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102282178 | TGTCTCAAAAAACAA[A/G]CAAACAAACAAACAA | 51366 |
rs779743576 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102313704 | AGATGATAAATAAAA[C/T]AGCCCTGAAGAAAGG | 51366 |
rs779746645 | snp | A/G | 1.65004e-05 | 0.00287227 | intron-variant | UBR5 | GRCh38.p7 | 8:102295386 | CATATTGCTTCCCAC[A/G]AGTGTCATAAATGTC | 51366 |
rs779792702 | snp | A/C/T | 5.9001e-05 | 0.00543117 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102345428 | CTGGAAAGTGATGAA[A/C/T]GACGAAAAGAAGGGT | 51366 |
rs779799597 | snp | C/T | 1.64912e-05 | 0.00287147 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295487 | ACAATGCTCCACCGT[C/T]TGCCTTGCGACTGTC | 51366 |
rs779813090 | snp | C/T | 1.64871e-05 | 0.00287111 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102278904 | ATAAAGACCCTGACT[C/T]GGACGGCCAAAAAGA | 51366 |
rs779818479 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102260565 | TCCTTTTGCTACAAT[-/A]AACAATAACTATTAA | 51366 |
rs779818841 | snp | C/T | 1.74287e-05 | 0.00295196 | intron-variant | UBR5 | GRCh38.p7 | 8:102285811 | GACAACCACAATGAG[C/T]TAATGTCAGTTGCTA | 51366 |
rs779820477 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102393953 | ACAATAAAAAGTTTC[C/T]AGAGGAAAAAATATT | 51366 |
rs779829753 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102288300 | TTGTAGACAATCAAA[A/G]CTAGTTAACTAAAAT | 51366 |
rs779834618 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102268917 | GATATGATGGCACCC[A/T]CATACTGAAAGTAAG | 51366 |
rs779847081 | snp | A/G | 1.85156e-05 | 0.00304261 | intron-variant, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102258950 | TGACCTATCTATATA[A/G]TTCATTCTTTAAACA | 51366 |
rs779898661 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102363000 | GGAATTACAGGTACC[C/T]GCCACCACACCCGGC | 51366 |
rs779904416 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102376951 | TATTCACAAAAGTAG[A/G]GGTCTGTTTAGGGAG | 51366 |
rs779913810 | snp | C/G | 1.65455e-05 | 0.00287619 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102297591 | TCTTCCTCTTTTTCA[C/G]TTGAGGATATTTCAG | 51366 |
rs779917662 | snp | A/G | 1.74439e-05 | 0.00295325 | intron-variant | UBR5 | GRCh38.p7 | 8:102285077 | AAAAATTGTAAGTTG[A/G]GGATCCATTTTAAGT | 51366 |
rs779918625 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102349229 | AAGGAAATTAAAAAA[-/A]CAATCCAGGCTGGGC | 51366 |
rs779919709 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102338375 | TCCTATTACACTAAA[C/T]TATTACTATAATAAA | 51366 |
rs779934003 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102372845 | GAAATTCTTATATTG[C/T]ACCACAAATAACACT | 51366 |
rs779964845 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102274259 | GAGTCTCTCACACTA[C/T]GTTGCCCAGGCTGTC | 51366 |
rs779969146 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102400800 | AGAAGCGAACAAAAA[A/T]AAACTACTCTAGCTT | 51366 |
rs780006449 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102382716 | TTGCAAAGACAAAAG[C/G]AGGCTTTAAGTCTCT | 51366 |
rs780008457 | snp | A/G | 1.64993e-05 | 0.00287218 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102259086 | GCCGTTAAATCTTCT[A/G]ATGAATTTTTTGGAA | 51366 |
rs780017296 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102339906 | CCAAGTTTACTATTG[C/T]GTACAAAATTGAGAC | 51366 |
rs780021202 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102324508 | CCAACAGTATCTCCA[C/T]CTTAGATAGGAACAT | 51366 |
rs780031356 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303190 | ATAGTCCTGAATAAA[C/T]AAACTGGTGATAATT | 51366 |
rs780041889 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102371275 | ATATCCTTTTTTTTT[-/A]AAAAAAAAAAAAAAA | 51366 |
rs780060126 | in-del | -/AAACCTTT | 1.68267e-05 | 0.00290053 | frameshift-variant, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102293721 | GGTGCAGTTGGACGA[-/AAACCTTT]GCAATCCCCATTCTG | 51366 |
rs780063717 | snp | G/T | 1.64958e-05 | 0.00287187 | intron-variant | UBR5 | GRCh38.p7 | 8:102360195 | TCAACTTTGACCTGG[G/T]GGAAAGCAAGAGGTA | 51366 |
rs780065433 | snp | G/T | | | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102327833 | GAAGTTCAGAGTAAG[G/T]CTGAGCAGTGTGCTC | 51366 |
rs780067941 | snp | A/C | 1.6698e-05 | 0.00288941 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102323465 | ATGCAACTGCTCCAG[A/C]ATGATAAAGAGGATT | 51366 |
rs780070343 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102326175 | TCATGCTGACAACAT[C/G]CTCATAGAGCAGTAT | 51366 |
rs780081117 | in-del | -/CAGTTTCTATCCACTGTAACCTCCATTAAA | 1.64966e-05 | 0.00287194 | cds-indel, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102278833 | TGTCTTACCTCTAGG[lengthTooLong]CATTTCCCACTACTG | 51366 |
rs780096824 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102389018 | TGTTTTCAAATACAT[C/G]GTATCAGTCTTTTCT | 51366 |
rs780123400 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102265032 | CATTTTAAAACAAAT[A/G]TATTTTAGAAAATCT | 51366 |
rs780124408 | snp | C/T | 4.94287e-05 | 0.00497111 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102329154 | AGGACTATCTTTTCA[C/T]TGGTTAACCCCAAAA | 51366 |
rs780124501 | snp | A/G | 1.65198e-05 | 0.00287395 | intron-variant | UBR5 | GRCh38.p7 | 8:102360561 | AAGAGCTAAATACAT[A/G]TTAAATAGAAAGGAC | 51366 |
rs780128670 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102383631 | TAGCTATGAAGTTGT[C/T]ATACATCCAACCACC | 51366 |
rs780139004 | in-del | -/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102360002 | AGATGATCATTCAGA[-/C]TGAGAGCACTCACAG | 51366 |
rs780141572 | snp | C/T | 3.30639e-05 | 0.00406581 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295092 | GCAAAAGATGGCCTA[C/T]TCTACTGCTGGCACT | 51366 |
rs780149438 | snp | C/T | 1.77798e-05 | 0.00298154 | intron-variant | UBR5 | GRCh38.p7 | 8:102298366 | CCAAACTGAATGTAA[C/T]TCATTTAGGATCTGA | 51366 |
rs780176393 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102278209 | TTTAATGTTTTACTA[C/T]TTTTTCAGTGGACAA | 51366 |
rs780184852 | snp | C/T | 1.66888e-05 | 0.00288862 | intron-variant | UBR5 | GRCh38.p7 | 8:102312512 | GGCAAATTCAATGAA[C/T]ATTAGCAATAGCTTA | 51366 |
rs780191538 | in-del | -/ACATACACAA | 1.71217e-05 | 0.00292584 | intron-variant | UBR5 | GRCh38.p7 | 8:102327695 | AAAGCATCTTTCTAT[-/ACATACACAA]GCATTCACCGATAAA | 51366 |
rs780193235 | snp | A/C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102365419 | CAGGATCAGTGAGCC[A/C/G]AGATCGCGCCACCGT | 51366 |
rs780194729 | snp | A/G | 3.31389e-05 | 0.00407042 | intron-variant | UBR5 | GRCh38.p7 | 8:102311521 | TGGGAAAATGGTAAA[A/G]TTTGACTCCTAATCA | 51366 |
rs780200392 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102276360 | CCTCCTCTTCCTTCA[A/G]AGTGATCAAGTCCAT | 51366 |
rs780202743 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102371401 | GGACGCATTCCACCA[C/T]GGCCAGCATTGGATA | 51366 |
rs780219154 | snp | C/T | 1.65072e-05 | 0.00287286 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102275749 | CCATGAATACCCTGC[C/T]GAACAGTTCTAAAGA | 51366 |
rs780246073 | snp | G/T | 1.65206e-05 | 0.00287403 | intron-variant | UBR5 | GRCh38.p7 | 8:102329266 | TATTCAATGCAAGAT[G/T]TCATAAAATAAAATA | 51366 |
rs780266111 | in-del | -/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102339543 | CAAAAAAAAAAAAAA[-/G]GGTAAAATTTTGAAG | 51366 |
rs780273908 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102277733 | AGCGCGGTGGCTCAC[G/T]CCTGTAATCCTAGCA | 51366 |
rs780278868 | in-del | -/AATTT | 3.38032e-05 | 0.00411102 | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102304196 | GAAAAAATTAAGATC[-/AATTT]AAGTTTTAGAACTAA | 51366 |
rs780285849 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102378487 | CGTCTCTACTAAAAA[C/T]ACAAAAATTAGCCGG | 51366 |
rs780302717 | snp | C/G | 1.72006e-05 | 0.00293258 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102294105 | AGTGTACCTAGTAGA[C/G]TATCTAAAAGCTTTA | 51366 |
rs780303855 | snp | C/G | 4.24277e-05 | 0.00460566 | intron-variant | UBR5 | GRCh38.p7 | 8:102264599 | ATTTAAATAATTCTA[C/G]AATACATATATCCCC | 51366 |
rs780310051 | snp | C/G | 1.68995e-05 | 0.00290679 | intron-variant | UBR5 | GRCh38.p7 | 8:102275860 | GGAAGGGGTGGGGGG[C/G]AGAAATAATTTAGCC | 51366 |
rs780310119 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102410131 | GCTGATTGTTTATAC[C/T]AGGAATGGAAAAAGA | 51366 |
rs780312257 | snp | A/G | 1.66615e-05 | 0.00288626 | missense, upstream-variant-2KB, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102304161 | TATTTCTTTCAGAAC[A/G]CTCCGCTTCTGAAAA | 51366 |
rs780321798 | snp | C/G | 1.64743e-05 | 0.00287 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102286469 | AGCACCATTGGCATG[C/G]GAGCTATTTGTGGTT | 51366 |
rs780322893 | snp | A/G | 1.64933e-05 | 0.00287165 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102312384 | ACAATCCTGCAGGAG[A/G]GAAGAAGGGTCAGCA | 51366 |
rs780341852 | snp | A/G | 1.67072e-05 | 0.00289021 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102286598 | ATCTTCAGAAAAGAA[A/G]GCAGGAACACTGCTT | 51366 |
rs780343841 | snp | A/G | 1.66685e-05 | 0.00288686 | intron-variant | UBR5 | GRCh38.p7 | 8:102279218 | TAGCACCTAAACATA[A/G]AAAGATAAAATGTTT | 51366 |
rs780348002 | snp | A/G | | | utr-variant-3-prime | UBR5 | GRCh38.p7 | 8:102252744 | ATCATTCAGTTTTAA[A/G]TATTTTTAGTGTTAA | 51366 |
rs780389814 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102408904 | GTAGTTGTATCCCTG[C/G]ATAAACACTGTAAAT | 51366 |
rs780401079 | snp | A/G | | | intron-variant, downstream-variant-500B, nc-transcript-variant | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102251868 | ACTTACTGAATCAGA[A/G]AGGAGGCAAGAGGAT | 51366 |
rs780416382 | snp | C/T | 1.64866e-05 | 0.00287106 | intron-variant | UBR5 | GRCh38.p7 | 8:102287414 | TAAGCAAGAAAGTAG[C/T]TGGGATAAGGCAACA | 51366 |
rs780431828 | snp | C/T | 3.30158e-05 | 0.00406286 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102280445 | CTTCATTATCAATAC[C/T]CAGTTCCAAGAGTTC | 51366 |
rs780461595 | snp | C/T | 1.64996e-05 | 0.0028722 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102347038 | TCGAGCTCCAGCTGA[C/T]GACCTACCAGAGGAT | 51366 |
rs780508287 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102398295 | ATAAAACTAGACCTC[-/T]TGTCTCTCACCATAC | 51366 |
rs780514158 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102334853 | CAAGGAGCCGAGATC[A/G]TGCCACTGCACTCCA | 51366 |
rs780528883 | in-del | -/A/AATA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102323092 | TTAAAGTATAATAAT[-/A/AATA]AATAAATTAATTAAT | 51366 |
rs780579895 | snp | A/G | 2.55751e-05 | 0.00357588 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102345432 | AAAGTGATGAACGAC[A/G]AAAAGAAGGGTAACC | 51366 |
rs780581220 | snp | A/G | 1.64866e-05 | 0.00287106 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102326574 | GTGATGTTCGGCATT[A/G]AAGAAATACCAGCAC | 51366 |
rs780583442 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102367427 | TTTACTGGTGCCAAC[A/T]TCTAGAAGGCACATC | 51366 |
rs780594760 | snp | C/T | 8.62032e-05 | 0.00656461 | intron-variant | UBR5 | GRCh38.p7 | 8:102346891 | ACATTAAGTGTTCTA[C/T]GAGATCCATACCTGT | 51366 |
rs780602434 | snp | G/T | 4.99272e-05 | 0.00499611 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102300147 | TCATTTCCCGTAATC[G/T]CAAACTAAAAGAACA | 51366 |
rs780632416 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102333672 | CTGAATTTTGCCCCA[C/G]AAAACTTGGTTTTCA | 51366 |
rs780642401 | snp | C/G | 0.000114462 | 0.00756426 | intron-variant, upstream-variant-2KB | UBR5, LOC105375683 | GRCh38.p7 | 8:102412129 | AGGGGAGGGAGGGAA[C/G]GGCGCCCCTCCCCCC | 51366 |
rs780649040 | snp | G/T | 1.65315e-05 | 0.00287498 | intron-variant | UBR5 | GRCh38.p7 | 8:102295597 | CTGTGCTGCGCTCTT[G/T]TGATTTAACTTACTG | 51366 |
rs780652050 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102356359 | GAAGTCTGAGGCACG[A/C]GAATCACTTGAACCC | 51366 |
rs780653864 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102352302 | GACAGAGTGAGACTC[-/T]TGTCTCCAACAACAA | 51366 |
rs780653894 | snp | C/T | 1.64936e-05 | 0.00287168 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295498 | CCGTCTGCCTTGCGA[C/T]TGTCTGTACTAAGAA | 51366 |
rs780665987 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102287995 | ATGTATTATATATAG[C/T]GCCTAAATTTTCTAA | 51366 |
rs780702910 | snp | A/T | 1.65682e-05 | 0.00287817 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102323342 | TGCTAGCTTTTTCCA[A/T]GTTTTTCAAGCTTTC | 51366 |
rs780712410 | snp | A/G | 1.64917e-05 | 0.00287151 | intron-variant | UBR5 | GRCh38.p7 | 8:102289593 | TGTAAAGAATCAGAA[A/G]CTTATGAGTGGGCTC | 51366 |
rs780716044 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102375813 | TGCAGAGCCTGGCTG[G/T]CTAAGCGCCTTACAT | 51366 |
rs780719812 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102406924 | GAATGCCAAGACTTG[C/T]GCAAAAACACACTTT | 51366 |
rs780751036 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102326900 | ATTCATCAATTGCTT[-/T]TTTTTTTTTTTTTTT | 51366 |
rs780771731 | snp | A/G | 0.000249433 | 0.0111649 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295755 | CTCCCAACAATCACA[A/G]TAGGCTGTTGGTGAT | 51366 |
rs780782207 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102364610 | GAAACTTTCAAATGG[A/G]TTTTATACAGACATT | 51366 |
rs780786304 | snp | G/T | 1.65351e-05 | 0.00287528 | intron-variant | UBR5 | GRCh38.p7 | 8:102278960 | ATTTTAACAGAAATA[G/T]TCTAGTTACATTGAA | 51366 |
rs780800763 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102340141 | CGATCTTGTGATTAA[C/T]ATAGCCCCCATAAGT | 51366 |
rs780810096 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102316269 | AGTATAAATGGAAAG[C/G]AAACTAAACAATTTT | 51366 |
rs780829418 | in-del | -/AATA | 1.65776e-05 | 0.00287898 | intron-variant | UBR5 | GRCh38.p7 | 8:102278787 | GGACAAGTTGTCCTT[-/AATA]AATGTTATATTGCAA | 51366 |
rs780852120 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102395035 | CTCACGGTCTCCACA[C/T]GTGCTGTTCCTTCTG | 51366 |
rs780876975 | in-del | -/TAGTGCTTCCAGTAC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102337290 | TTGTTTGATGTTCAT[-/TAGTGCTTCCAGTAC]TAGTGCTTCCAGTAC | 51366 |
rs780877843 | snp | G/T | 4.96348e-05 | 0.00498146 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102279202 | TCCTTATCATTCAAA[G/T]TAGCACCTAAACATA | 51366 |
rs780877856 | snp | C/T | 1.65356e-05 | 0.00287533 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102270047 | TACACACTGGTTGCA[C/T]TGCTTGTACACGAGG | 51366 |
rs780883381 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102270307 | TTATGGTACCTAGGT[A/G]GTAGAGTGCCAAAAC | 51366 |
rs780887146 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102304373 | TGTGATTTATTTCCT[C/T]ATTCCGCCTTCCTTC | 51366 |
rs780893564 | snp | G/T | 1.68681e-05 | 0.00290409 | intron-variant | UBR5 | GRCh38.p7 | 8:102346193 | ACTCCCCAGTCGAAA[G/T]AGCACTCCAGAAATG | 51366 |
rs780900042 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102272144 | GAGCAAGTTTGGAAA[-/T]CATAATGTGAACAGC | 51366 |
rs780912475 | snp | A/G | 1.6477e-05 | 0.00287024 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102289550 | TGTGGATTCCTGATG[A/G]TGTAGGATGACTGAG | 51366 |
rs780914167 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102259796 | CTGGGTGTGGTGGCT[C/T]ATGCCTGTAATCCCA | 51366 |
rs780936083 | in-del | -/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102354143 | TGTGTATATTTATTT[-/C]CATGAAAATATCAAT | 51366 |
rs780946680 | snp | C/G | 1.69306e-05 | 0.00290947 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102323485 | TAAAGAGGATTATTT[C/G]TCAAGCATACCTAGC | 51366 |
rs780961735 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102352987 | GTTTCTCCATTCACC[G/T]GACTGTTACCATAGA | 51366 |
rs780963358 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102383812 | CCTACATCAAGGTAC[A/C]TCAGTGTGAAATTTC | 51366 |
rs780967037 | snp | C/G | 1.65222e-05 | 0.00287417 | intron-variant | UBR5 | GRCh38.p7 | 8:102295577 | GAGGCTGAAAAGCTA[C/G]TCAGCTGTGCTGCGC | 51366 |
rs780967416 | snp | G/T | | | intron-variant, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102258583 | ATTTGGGTCCAGCTC[G/T]ATAGAGCAATCATCA | 51366 |
rs780979539 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102382923 | CAGGAATAATTTTCC[C/T]GCATGTAACTTCTAG | 51366 |
rs780980979 | snp | A/C | 1.64966e-05 | 0.00287194 | intron-variant | UBR5 | GRCh38.p7 | 8:102360580 | AATAGAAAGGACATA[A/C]TATCTTACCCATCAT | 51366 |
rs780989282 | snp | A/G | 1.7383e-05 | 0.00294808 | intron-variant | UBR5 | GRCh38.p7 | 8:102285095 | ATCCATTTTAAGTTG[A/G]GGACGTTCTGTATAT | 51366 |
rs780999387 | snp | A/T | 1.88585e-05 | 0.00307065 | intron-variant | UBR5 | GRCh38.p7 | 8:102294125 | TAAAAGCTTTAAAAA[A/T]TTATATTCACTCTAT | 51366 |
rs781040382 | snp | C/T | 1.65241e-05 | 0.00287433 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102259118 | CACATCTAGTAGACC[C/T]TTCCTCATTGCCTAG | 51366 |
rs781049828 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102365938 | AAGTACAGGTTCTTC[A/G]GTTTCATAATTCTCT | 51366 |
rs781061126 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102328965 | CATTAGATTACTAAG[A/G]CTTGAGACACTTTGT | 51366 |
rs781076690 | snp | A/G | 5.52329e-05 | 0.00525484 | synonymous-codon, intron-variant | UBR5 | GRCh38.p7 | 8:102361593 | TTACCTGTTTAAATT[A/G]TATTTGTTCAGCTTC | 51366 |
rs781086506 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102353843 | AGATCAAGACTAGCC[C/T]GGGCAACCTGTCAAA | 51366 |
rs781110133 | in-del | -/T | 1.64792e-05 | 0.00287042 | intron-variant | UBR5 | GRCh38.p7 | 8:102268928 | CCCACATACTGAAAG[-/T]TAAGTAGCTGATGTT | 51366 |
rs781129440 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102392546 | TAAAGAAAATACAGG[-/A]AAAAAAAAAAGGTAA | 51366 |
rs781145340 | snp | C/T | 1.65034e-05 | 0.00287253 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102329312 | AAGGCTCAGATTCAC[C/T]CCATTTCCACTGATA | 51366 |
rs781152864 | in-del | -/CA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102351413 | CTGAAATAAGCCTGT[-/CA]CACACACACACACAA | 51366 |
rs781161144 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102410382 | ACAAGACAAGCACTA[C/T]CAACATGGTTCTGTT | 51366 |
rs781162783 | snp | A/G | 1.66214e-05 | 0.00288278 | intron-variant | UBR5 | GRCh38.p7 | 8:102311532 | TAAAGTTTGACTCCT[A/G]ATCAAAAAATGTATC | 51366 |
rs781174110 | snp | C/T | 1.6504e-05 | 0.00287258 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102329316 | CTCAGATTCACTCCA[C/T]TTCCACTGATAAAGT | 51366 |
rs781176935 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102290833 | TACCAATACATAAAA[C/T]GTATTACAGTTGAAC | 51366 |
rs781194226 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102341069 | AAACTTACACTATTC[A/G]GAAATACTTTCATTA | 51366 |
rs781199929 | in-del | -/A | 3.49669e-05 | 0.00418117 | intron-variant | UBR5 | GRCh38.p7 | 8:102300198 | ACCATATCTACACAT[-/A]AATGAAACGGTGTAC | 51366 |
rs781200195 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102285851 | CTCTGGGATTATATA[C/T]ACTTACGTAAATCTA | 51366 |
rs781251137 | in-del | -/GAA | 1.674e-05 | 0.00289305 | intron-variant | UBR5 | GRCh38.p7 | 8:102299010 | GTACAAAACAACAAT[-/GAA]GAAGACACAGTAAAA | 51366 |
rs781268416 | snp | A/G | 1.68105e-05 | 0.00289914 | intron-variant | UBR5 | GRCh38.p7 | 8:102312529 | TTAGCAATAGCTTAT[A/G]TAAAATCAACATACA | 51366 |
rs781268764 | snp | A/G | 0.00013256 | 0.00814018 | intron-variant | UBR5 | GRCh38.p7 | 8:102278792 | AGTTGTCCTTAATAA[A/G]TGTTATATTGCAAAA | 51366 |
rs781284990 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102374326 | GAACTTGAGGATCCA[C/G]GGAATGAAAGCTAAG | 51366 |
rs781305697 | snp | A/G | 1.65351e-05 | 0.00287528 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295111 | ACTGCTGGCACTAAG[A/G]CTTGAGGAGAAACGA | 51366 |
rs781310882 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102379184 | GAGTAGGGGTATATG[C/T]GAACACTAAACTCAT | 51366 |
rs781323324 | snp | G/T | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102305170 | ATTTCCATCACATCT[G/T]TGGCTGATGAATGTC | 51366 |
rs781331442 | snp | A/T | 1.64961e-05 | 0.00287189 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102287489 | CGCCCACTAGCATTA[A/T]CTTGGTTGCTGTGGT | 51366 |
rs781335697 | snp | A/T | | | intron-variant, upstream-variant-2KB | UBR5 | GRCh38.p7 | 8:102303814 | AGAACAAATTGAAAG[A/T]AACAAATTTAAACTA | 51366 |
rs781350883 | snp | C/G | 1.64906e-05 | 0.00287142 | intron-variant | UBR5 | GRCh38.p7 | 8:102266915 | TAATTTAAATTCTGT[C/G]ATTATCAGCACATGA | 51366 |
rs781367181 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102359859 | ATTTTTTAAAGGTCA[A/G]GAGCCTAGATTAATT | 51366 |
rs781378122 | snp | C/T | 3.35182e-05 | 0.00409365 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102295774 | GCTGTTGGTGATGTC[C/T]GTTTGAGTCTATAGA | 51366 |
rs781391251 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102280332 | GAAGTTAAAAAGCTT[G/T]AAGGGGAACTACTGA | 51366 |
rs781407675 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102390992 | ATTTGGGAGGCCGAG[A/G]CGGGAGAATCCCTAG | 51366 |
rs781415502 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102403267 | AGAAATAAATAAGGC[A/G]AGGCACAGTGGTTCA | 51366 |
rs781420205 | in-del | -/T | 1.65168e-05 | 0.00287369 | intron-variant | UBR5 | GRCh38.p7 | 8:102295567 | CGTGAGGAGGGAGGC[-/T]GAAAAGCTACTCAGC | 51366 |
rs781428180 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | UBR5 | GRCh38.p7 | 8:102253764 | AAACCGCAATAAAAG[C/T]GGTTTTTATAGGTAA | 51366 |
rs781450808 | snp | G/T | 2.00729e-05 | 0.00316797 | intron-variant | UBR5 | GRCh38.p7 | 8:102286632 | CCTAAAATTTTTATT[G/T]TTAAAACCAAAAACA | 51366 |
rs781474039 | snp | C/G | 1.65457e-05 | 0.00287621 | synonymous-codon, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102281294 | GAATGGATACCTTTT[C/G]CGTTCTAGTTGAGGT | 51366 |
rs781476037 | snp | C/G | 1.64773e-05 | 0.00287026 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102272563 | GGCATTTTGGATACA[C/G]TCTAGATTTGGCAAT | 51366 |
rs781506636 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102410283 | CCAACTGAGTAAGCT[A/T]GTCAGGTTTCTTGGT | 51366 |
rs781533765 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102274078 | AGCTGGTAGCAAAAC[C/T]TACAAAGAAGAATTA | 51366 |
rs781567939 | snp | C/T | 1.6489e-05 | 0.00287128 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102272705 | GGTGTAGTAGCACAT[C/T]TTCGACCAAAGTGAT | 51366 |
rs781585909 | snp | C/T | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102305246 | TTCATTAGATATTGT[C/T]GACAGGCCTCATAGT | 51366 |
rs781607363 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102369874 | TGCTTTGATTTCTGC[C/T]AAAAAGCCAGTATTT | 51366 |
rs781620887 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102381389 | ACAAACAAAACCATC[A/C]GATCTCATGAGAACT | 51366 |
rs781635152 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102288134 | ACTCATACTGAGTAA[C/T]TTCTCAAATAACCTG | 51366 |
rs781638538 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102379921 | AGTAAAAGAGACTGG[C/G]TGCCAGAGCTGGGTT | 51366 |
rs781658503 | snp | A/G | 1.70971e-05 | 0.00292374 | intron-variant | UBR5 | GRCh38.p7 | 8:102346895 | TAAGTGTTCTACGAG[A/G]TCCATACCTGTGAAA | 51366 |
rs781672698 | in-del | -/TTTGT | | | intron-variant | UBR5 | GRCh38.p7 | 8:102371581 | CCTGATTCTGGGTTG[-/TTTGT]TTTTTTTTTTTTTGA | 51366 |
rs781709329 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102355235 | CACTTCCTGATCCAG[A/G]ACAACTCCCAGCAGC | 51366 |
rs781729881 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102270768 | AGATGATCCACCCAC[C/T]TCGGCCTCCCAAAGT | 51366 |
rs781740289 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102273084 | CAAATGATCAGAGAT[A/G]TTAAAAAAAAAATAC | 51366 |
rs781759704 | snp | G/T | 1.65217e-05 | 0.00287412 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102293626 | GACTGATCAGATGAT[G/T]GTCGTGGTGGTAGTG | 51366 |
rs781767695 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102325467 | TAAGGATTAAGTTTT[G/T]AAACATTCATAACAG | 51366 |
rs781782728 | snp | C/T | 1.69778e-05 | 0.00291352 | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102293762 | TCAGTGACTCTGCTA[C/T]GTTGCACAATTCTTC | 51366 |
rs796052149 | snp | A/G | | | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102281379 | TTTGCTCATTGAAGC[A/G]TGTGGCATATGTTTT | 51366 |
rs796076867 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102321766 | ATGGAACAGAACAGA[C/G]CCCTCAGAAATAATG | 51366 |
rs796081144 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102381465 | CAATCACCTCCCATC[A/G]TGTCCCTCCCTTGAC | 51366 |
rs796090229 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102396721 | ATATATTTTTTTTTT[-/T]CTTGAGACAGAGTCT | 51366 |
rs796095662 | in-del | -/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102301865 | GTGTAAGAAATGGGG[-/G]TAGTGACAAGCTAGA | 51366 |
rs796099924 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102339803 | AAAAACTTCATTGCT[C/G]CATCTGCCATTTACA | 51366 |
rs796109958 | in-del | -/AA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102287188 | AAAAAAAAAAAAAAA[-/AA]GGCAAGAAAATAAAA | 51366 |
rs796132513 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102293247 | TCATTTTCATACATA[C/T]TAAAGTTTGAGAAGC | 51366 |
rs796168108 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102410800 | GGAAGCGCATGACAA[A/G]CAGGGCATCATGCAA | 51366 |
rs796187556 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102309344 | ACAGGTACAATCCAC[C/G]ATGCCCGACTGTGTA | 51366 |
rs796212873 | in-del | -/AC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102396649 | CACACATATATATAT[-/AC]ACACACACACACACA | 51366 |
rs796232496 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102374041 | TTTTAACATCCCAGA[A/G]GCATGGAAGGTTTCT | 51366 |
rs796239537 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102377142 | ATGGAACACTCGCTA[A/G]TAAGATCTTGGGGAA | 51366 |
rs796252691 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102404522 | GACCCCATGGAAAAA[C/T]CACTGAATTTCAAGA | 51366 |
rs796264766 | snp | C/T | | | missense, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102314780 | TGGCAATTGAGGATG[C/T]ATCACTACACGTGGA | 51366 |
rs796299827 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102277821 | CCAACAAAGCGAAAC[C/G]CTGTCTCTACTAAAA | 51366 |
rs796303315 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102407119 | TTAATTTTTTTTTCC[-/T]TTTTTTTTGAGACAG | 51366 |
rs796317555 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102313049 | CACAGAATTTGAAAC[C/G]AGGACAAATTTGGGT | 51366 |
rs796342024 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102270273 | AAAGTTAGAAAACCA[C/G]AGCATATAGGTTGTT | 51366 |
rs796369647 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102379037 | CCTTTTTTGCCGTGC[-/T]TTTTTTTTTTTTTAA | 51366 |
rs796373383 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102267602 | GGCAGAGGAATAAAC[A/G]AACAGTACATAAAAT | 51366 |
rs796404703 | in-del | -/A | | | intron-variant | UBR5 | GRCh38.p7 | 8:102329038 | GCAAAAAAGAAAAAA[-/A]GAAAACAAGAATTAA | 51366 |
rs796419088 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102335369 | ATGTCATGAGGATTA[C/T]AGTTAATAAAATGGT | 51366 |
rs796420483 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102367199 | TTCTTAAGTAAACAG[G/T]CAGTCAGTCCTCAAT | 51366 |
rs796425614 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102371936 | GCTGGTTATGATGGC[G/T]CATGCCTGTAATCTC | 51366 |
rs796448694 | in-del | -/GGG | | | intron-variant | UBR5 | GRCh38.p7 | 8:102283342 | TAGGAAGGGGAAGGC[-/GGG]GGGGGGGGGGGGTGA | 51366 |
rs796488462 | in-del | -/ATA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102387274 | AAACAATAATTTACT[-/ATA]ATGTCAGTTTCTATC | 51366 |
rs796494857 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102401533 | GCAGAAAGATGAACA[A/G]ATGCCAACAAAATCA | 51366 |
rs796509131 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102307273 | TAAAATCTGGATTTT[A/T]AATGTAAATCCTGTG | 51366 |
rs796523165 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102353970 | CAGGAGGCGGAGGCT[G/T]CAATAAGCCAAAATC | 51366 |
rs796564019 | in-del | -/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102309111 | AGGCTGGAGTGCAGT[-/G]GCATGATCTCAGCTC | 51366 |
rs796567075 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102263372 | CCACCCTGGGTGACA[C/G]AGTGAGACTGTCTCA | 51366 |
rs796581862 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102386705 | CATATAGGCCGGGCG[C/T]GGTGGCTCATGCCTG | 51366 |
rs796582885 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102357649 | TGGACAAAAGGGTAT[-/T]AGTGGACAACTGGAG | 51366 |
rs796583926 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102287668 | ACTAAGAAGGCATAG[G/T]GGGTAGGAGTTGGGG | 51366 |
rs796611325 | in-del | -/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102308818 | AAAATTTTAAATATA[-/G]GAAAAAGTGCTTAAT | 51366 |
rs796627564 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102336499 | TTTTTAAGGTTTCAT[A/G]TTTCACATTTAGGTC | 51366 |
rs796652702 | in-del | -/GGAA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102387722 | AAAAAAAAAAAAAAT[-/GGAA]GGAAGGAAGGAAGGA | 51366 |
rs796708318 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102400629 | TCATAGTGCTACTAT[A/C]TATGGATGAGCCTCA | 51366 |
rs796719904 | in-del | -/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102306012 | GCTGGGCATGAGCAA[-/C]CCACACCCAGCCCTC | 51366 |
rs796729644 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102353326 | TCCTACAATTTTGAT[C/G]CCGTTATACAGTTCT | 51366 |
rs796737751 | snp | A/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102340085 | TCACCACCTGTCTCC[A/T]GCACTAAACCTCACA | 51366 |
rs796752582 | in-del | -/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102371585 | ATTCTGGGTTGTTTG[-/T]TTTTTTTTTTTTTGA | 51366 |
rs796797202 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102386456 | AAGAAAAATGAGCAC[A/G]GAGACTGTCACTTTA | 51366 |
rs796799415 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102342109 | TGACTTTAGAAATTT[C/G]ACAAAACAAATTTCT | 51366 |
rs796818818 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102276203 | AAATAAATATGTCCA[C/T]GTCAACGATGCTCAA | 51366 |
rs796851037 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102284933 | TCCCAGCTACTCGGG[A/C]GGCTGGGGCAGGAGA | 51366 |
rs796893011 | snp | A/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102283351 | GAAGGCGGGGGGGGG[A/G]GGGGGTGAGTAGGGG | 51366 |
rs796898755 | snp | A/C | | | intron-variant, nc-transcript-variant | UBR5 | GRCh38.p7 | 8:102258852 | AAAACAATGTAAAAA[A/C]TTGTTTTAATGCTTG | 51366 |
rs796900052 | in-del | -/AA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102372983 | CACACACACACACAC[-/AA]TCAGTCATGTTCCTT | 51366 |
rs796900073 | snp | A/C | | | intron-variant | UBR5 | GRCh38.p7 | 8:102384469 | CACTCAGGGAGGCCA[A/C]GGCAGGAGGAACACA | 51366 |
rs796901086 | in-del | -/AC | | | intron-variant | UBR5 | GRCh38.p7 | 8:102361979 | CAATTGTTTAAAAAA[-/AC]AAAACAAAACAAAAA | 51366 |
rs796919807 | in-del | CC/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102277693 | CCTTACCCACCCCCC[CC/T]CCTTTAAATTCACTT | 51366 |
rs796926298 | snp | C/G | | | intron-variant | UBR5 | GRCh38.p7 | 8:102321474 | ACATTCCATGCTCAT[C/G]GGTAGGAAGAATCAA | 51366 |
rs796928998 | in-del | -/TA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102312495 | TAGCACCTGGAAGTA[-/TA]GGCAAATTCAATGAA | 51366 |
rs796972471 | multinucleotide-polymorphism | CG/GA | | | intron-variant | UBR5 | GRCh38.p7 | 8:102399065 | GGGCATGGAAACAGG[CG/GA]TTAAAAAAAGACCAA | 51366 |
rs796983942 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102332987 | AACAAACCAGCCCAA[G/T]AGCAAGAGCATGGTG | 51366 |
rs796988923 | in-del | -/TAAA | | | intron-variant, downstream-variant-500B, nc-transcript-variant | UBR5, UBR5-AS1 | GRCh38.p7 | 8:102252065 | TTTGGGGGCAGCTAC[-/TAAA]TAGTGAAATCATTCC | 51366 |
rs797014048 | snp | G/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102267894 | ACCTATCTTCCCTTT[G/T]TTTTTCTTTTTTTTT | 51366 |
rs797018627 | snp | C/T | | | intron-variant | UBR5 | GRCh38.p7 | 8:102409664 | TATTGCCCCAACTTA[C/T]TAAAACTTGGTAAAG | 51366 |