SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs12584 | snp | A/T | 0.486235 | 0.0818856 | missense | UBR4 | GRCh38.p7 | 1:19086767 | GTAGCCTTGGAGGAG[A/T]TGGAGAATAAGCCCC | 23352 |
rs732725 | snp | A/G | 0.418491 | 0.184691 | intron-variant | UBR4 | GRCh38.p7 | 1:19088320 | AGTCTGTGCTTTGGA[A/G]AAGGAGCTTGTAGGA | 23352 |
rs841371 | snp | A/G | 0.081446 | 0.184634 | intron-variant | UBR4 | GRCh38.p7 | 1:19186022 | CCCTTCGTATTTCAC[A/G]TTGTTCCCACAAACC | 23352 |
rs841372 | snp | C/T | 0.081446 | 0.184634 | intron-variant | UBR4 | GRCh38.p7 | 1:19186739 | CTCCATAATCTCTTT[C/T]ATTTTTTCCTAAATC | 23352 |
rs841373 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBR4 | GRCh38.p7 | 1:19198126 | AGTGAGCAGTAGCTG[C/T]ACGGATACTCTCCAG | 23352 |
rs841374 | snp | C/T | 0.429238 | 0.174281 | intron-variant | UBR4 | GRCh38.p7 | 1:19199091 | ACCGTATGTAGCTTA[C/T]AGATTTGTCTTATTG | 23352 |
rs870482 | snp | C/T | 0.154661 | 0.231107 | intron-variant | UBR4 | GRCh38.p7 | 1:19173834 | GAAATGTGCAGAATA[C/T]GGAACAAATTATTTG | 23352 |
rs942179 | snp | A/G | 0.40595 | 0.195396 | intron-variant | UBR4 | GRCh38.p7 | 1:19122320 | AAAGTAAACTGGATT[A/G]TAGTTTCTTAGGTCA | 23352 |
rs942180 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBR4 | GRCh38.p7 | 1:19105367 | CTGAATGCTTCCTAG[A/G]TGTGGGAAATTCCCA | 23352 |
rs942181 | snp | C/T | 0.455502 | 0.142369 | intron-variant | UBR4 | GRCh38.p7 | 1:19099065 | TGGGCCTTTTGGCCA[C/T]CACGAGTGATGCTGT | 23352 |
rs942182 | snp | C/T | 0.15665 | 0.231917 | intron-variant | UBR4 | GRCh38.p7 | 1:19150087 | GTCTCCCTACAGTGG[C/T]ATATTCTTAAGCATT | 23352 |
rs946419 | snp | A/G | 0.405776 | 0.195535 | intron-variant | UBR4 | GRCh38.p7 | 1:19160345 | CAAGATGATTTTTAC[A/G]AGTATTATCCATTGT | 23352 |
rs951908 | snp | C/G | 0.459727 | 0.136069 | intron-variant | UBR4 | GRCh38.p7 | 1:19173341 | AGCTTTGCCTATAGT[C/G]ATCTCCTAAACACTT | 23352 |
rs952789 | snp | G/T | 0.0652144 | 0.168387 | intron-variant | UBR4 | GRCh38.p7 | 1:19173379 | TCTTCAAATTTAAAA[G/T]CTCCAGTAAGCACAA | 23352 |
rs952790 | snp | A/G | 0.143602 | 0.226229 | synonymous-codon | UBR4 | GRCh38.p7 | 1:19173460 | CCAGTTGACATAGGA[A/G]CTGATCCGGAGCCGA | 23352 |
rs1009806 | snp | C/T | 0.44858 | 0.151875 | intron-variant | UBR4 | GRCh38.p7 | 1:19174057 | ACACATCAACCAGTA[C/T]TGACAGGAGATATAG | 23352 |
rs1043899 | snp | A/G | 0.48697 | 0.0796554 | synonymous-codon | UBR4 | GRCh38.p7 | 1:19088810 | CCGGGCAGAGAAGAA[A/G]CGCATGGCCATGGCA | 23352 |
rs1043905 | snp | C/T | 0.458106 | 0.138556 | synonymous-codon | UBR4 | GRCh38.p7 | 1:19084635 | TCAGCTCAACATCCA[C/T]GACATCAAACTGCTC | 23352 |
rs1044010 | snp | C/G | 0.486186 | 0.0819531 | synonymous-codon | UBR4 | GRCh38.p7 | 1:19121349 | GCTCTCCTGTGCTCT[C/G]TGCGGCAGCAAGGTG | 23352 |
rs1106839 | snp | A/G | 0.458435 | 0.13804 | intron-variant | UBR4 | GRCh38.p7 | 1:19093898 | TCACAGACCTAGTTC[A/G]GCGTTTTAGTGGAGA | 23352 |
rs1138838 | snp | A/G | 0 | 0 | intron-variant | UBR4 | GRCh38.p7 | 1:19102213 | tacaaaaaaatacat[A/G]aattggccaggcgtg | 23352 |
rs1339119 | snp | A/G | | | intron-variant | UBR4 | GRCh38.p7 | 1:19149119 | ACAAACTATTTTTTA[A/G]GTGCATGCCAATTGC | 23352 |
rs1538485 | snp | A/C | 0.0930568 | 0.194599 | intron-variant | UBR4 | GRCh38.p7 | 1:19178549 | GGGAACAGAAAGCAA[A/C]GCCTTTTAGGAAAAC | 23352 |
rs1538486 | snp | A/T | | | intron-variant | UBR4 | GRCh38.p7 | 1:19186465 | GTTTGGTCAGGAAAC[A/T]ACAGGAATCTGCTGA | 23352 |
rs1886024 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | UBR4 | GRCh38.p7 | 1:19075474 | CCTTAGCACATGCCT[C/T]GCGTTCTTCCCAGAA | 23352 |
rs1886025 | snp | C/T | 0.394721 | 0.203852 | intron-variant | UBR4 | GRCh38.p7 | 1:19075320 | AGGAAGGAGGGTCCC[C/T]TGGGCTCGAGCTCCA | 23352 |
rs1886026 | snp | C/T | 0.478104 | 0.102316 | intron-variant | UBR4 | GRCh38.p7 | 1:19075234 | GCCTTTGCCAGGCAG[C/T]GAGCCTCCGTGCCTT | 23352 |
rs1970369 | snp | A/G | 0.233818 | 0.249476 | intron-variant | UBR4 | GRCh38.p7 | 1:19180244 | cccaggcaggagtgc[A/G]gttgcacgatctcag | 23352 |
rs1970370 | snp | A/G | 0.406641 | 0.194842 | intron-variant | UBR4 | GRCh38.p7 | 1:19180250 | CAGGAGTGCGGTTGC[A/G]CGATCTCAGCTCACT | 23352 |
rs1970509 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBR4 | GRCh38.p7 | 1:19185549 | GCATGTAAATTATAC[C/T]CCAATAAAACTGAtt | 23352 |
rs1999967 | snp | G/T | 0.409891 | 0.192184 | intron-variant | UBR4 | GRCh38.p7 | 1:19162345 | CAAGCTTTTGGCTCT[G/T]TTTTCCAGCCTCCTG | 23352 |
rs2066002 | snp | A/G | 0.444267 | 0.157354 | intron-variant | UBR4 | GRCh38.p7 | 1:19177806 | CCCAGGAGTTATAAT[A/G]TCAAGCACTAGAAGA | 23352 |
rs2146865 | snp | C/G | 0.479663 | 0.0987666 | intron-variant | UBR4 | GRCh38.p7 | 1:19078790 | AGAGGCAGTCTCCCC[C/G]TGCCTGTCGCTCCCC | 23352 |
rs2146866 | snp | C/T | 0.473266 | 0.112482 | intron-variant | UBR4 | GRCh38.p7 | 1:19078743 | GCTGGTCTTTAATCC[C/T]GAACTGAATCATTGG | 23352 |
rs2146867 | snp | A/T | 0.394538 | 0.203982 | intron-variant | UBR4 | GRCh38.p7 | 1:19077577 | CCCGGCTAATTTTGT[A/T]TTTTTAGTAGAGATG | 23352 |
rs2181596 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | UBR4 | GRCh38.p7 | 1:19154483 | TGGGGGAGGAAGAGA[C/T]TTTCAACAAGTTTGC | 23352 |
rs2181597 | snp | C/T | 0.477175 | 0.104362 | intron-variant | UBR4 | GRCh38.p7 | 1:19077682 | GCAATGGCGTGATCT[C/T]GGCTCACTGCAACCT | 23352 |
rs2181598 | snp | C/G | 0.411631 | 0.207938 | intron-variant | UBR4 | GRCh38.p7 | 1:19077373 | AGGAAGACCTTCCCC[C/G]CCGGGTCTCTCTTTG | 23352 |
rs2236377 | snp | C/T | 0.458744 | 0.137571 | intron-variant | UBR4 | GRCh38.p7 | 1:19099705 | TACAATTATTTGGAA[C/T]AACAGCTTCACCTGC | 23352 |
rs2236378 | snp | C/T | 0.0285327 | 0.115984 | synonymous-codon | UBR4 | GRCh38.p7 | 1:19095566 | GAACACCTTGAACGT[C/T]ATGCTGGGGACCCTA | 23352 |
rs2274000 | snp | C/T | 0.0771179 | 0.180587 | synonymous-codon | UBR4 | GRCh38.p7 | 1:19144894 | AGGACTAACTCATAT[C/T]GAAGCTACTGTCAAT | 23352 |
rs2274001 | snp | A/G | 0.424037 | 0.179474 | intron-variant | UBR4 | GRCh38.p7 | 1:19138279 | TTATTGTCTAATGCT[A/G]TCAGTTACTGTCTTA | 23352 |
rs2274002 | snp | A/G | 0.0143368 | 0.0834438 | intron-variant | UBR4 | GRCh38.p7 | 1:19127593 | GGTTCATGGGTTTGG[A/G]GAAAGGTAAGCGGAT | 23352 |
rs2274003 | snp | C/T | 0.446118 | 0.155041 | intron-variant | UBR4 | GRCh38.p7 | 1:19114718 | CTTTACTTTCTAGCC[C/T]AAGCCTTCTTCGACT | 23352 |
rs2274004 | snp | C/T | 0.280256 | 0.248162 | intron-variant | UBR4 | GRCh38.p7 | 1:19114678 | TTTCAGGGCCCAGCT[C/T]TTGGGTGGGAGCAAA | 23352 |
rs2274005 | snp | A/T | 0.272241 | 0.249009 | intron-variant | UBR4 | GRCh38.p7 | 1:19114564 | TCTCCAGGTACAGAT[A/T]ACTTTGGATTTGGAT | 23352 |
rs2274006 | snp | C/T | 0.408188 | 0.193589 | intron-variant | UBR4 | GRCh38.p7 | 1:19095362 | GGCTGGCTCACCTCC[C/T]GCCCCCATGCTGCTG | 23352 |
rs2274007 | snp | A/C | 0.266 | 0.249487 | intron-variant | UBR4 | GRCh38.p7 | 1:19095352 | CCTCCTGCCCCCATG[A/C]TGCTGCCATGGCACT | 23352 |
rs2274008 | snp | A/C | 0.404733 | 0.196361 | intron-variant | UBR4 | GRCh38.p7 | 1:19086926 | TGAGAGCAACCTGAA[A/C]CCCAAGGCATTGCCC | 23352 |
rs2274009 | snp | A/G | 0.479583 | 0.0989539 | intron-variant | UBR4 | GRCh38.p7 | 1:19085970 | AGGGTGGGGGATGGA[A/G]GCTTACTCAAGGGGT | 23352 |
rs2274010 | snp | A/G | 0.000217856 | 0.0104346 | missense | UBR4 | GRCh38.p7 | 1:19078050 | CTGACAGATAAGGCA[A/G]TGAAGGACTATTCCG | 23352 |
rs2275401 | snp | A/G | 0.000378853 | 0.013758 | missense | UBR4 | GRCh38.p7 | 1:19167134 | AGATGCGTTCCAGGG[A/G]GTTGCTACTGATCTC | 23352 |
rs2281748 | snp | C/T | 0.483576 | 0.0892574 | intron-variant | UBR4 | GRCh38.p7 | 1:19074911 | TGACACACCTCTGCC[C/T]GTTGTGCTTTGCAGG | 23352 |
rs2282330 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | UBR4 | GRCh38.p7 | 1:19152105 | CTACACAGTAATCCT[A/G]CTGGTATTGGTGGAA | 23352 |
rs2282331 | snp | C/T | 0.499437 | 0.0167637 | intron-variant | UBR4 | GRCh38.p7 | 1:19154445 | ATGAAACTCTCACTA[C/T]CTTACACACCCCTCT | 23352 |
rs2296104 | snp | A/G | 0.405603 | 0.195673 | intron-variant | UBR4 | GRCh38.p7 | 1:19119894 | AGCTTCTGCTCTGGG[A/G]TATGTTGGGTGATGG | 23352 |
rs2296105 | snp | A/G | 0.478188 | 0.10213 | intron-variant | UBR4 | GRCh38.p7 | 1:19097071 | CAGAATTGTGGGGAG[A/G]TTGTTTCTTCAATTG | 23352 |
rs2296106 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBR4 | GRCh38.p7 | 1:19096744 | GAAAAGGGCTGTCAG[C/T]CATCAGCCAGGAATA | 23352 |
rs2296107 | snp | C/G | 0.445855 | 0.155373 | intron-variant | UBR4 | GRCh38.p7 | 1:19150155 | ACAGCCTCTCTTGCT[C/G]GCAATGTTATTATCA | 23352 |
rs2296108 | snp | A/C | 0.499437 | 0.0167637 | intron-variant | UBR4 | GRCh38.p7 | 1:19148481 | GGCCCTGAGGCCTCG[A/C]AGCTAAAGAACATTT | 23352 |
rs2296109 | snp | C/G | 0.424037 | 0.179474 | intron-variant | UBR4 | GRCh38.p7 | 1:19144255 | TGCCAGAACAGGAAG[C/G]GGGGATTAACTTAAC | 23352 |
rs2313165 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | UBR4 | GRCh38.p7 | 1:19075536 | AGAGCCAGTGGGAGC[C/T]GTAAAGAGGTGGTGG | 23352 |
rs2313506 | snp | C/T | 0.0872718 | 0.189788 | intron-variant | UBR4 | GRCh38.p7 | 1:19084916 | ACTGAACGTGACACT[C/T]GCCAAGTTTTGATGA | 23352 |
rs2313507 | snp | C/T | 0.479663 | 0.0987666 | intron-variant | UBR4 | GRCh38.p7 | 1:19084950 | CCCACCACTCTTGGG[C/T]GCCCATTTCTTAATG | 23352 |
rs2313508 | snp | C/T | 0.0872718 | 0.189788 | intron-variant | UBR4 | GRCh38.p7 | 1:19085006 | GCTGCATGTGGAGTA[C/T]ATTTTGGAGGAAGCA | 23352 |
rs2313509 | snp | C/T | 0.448452 | 0.152042 | intron-variant | UBR4 | GRCh38.p7 | 1:19111366 | ATGGGATCTGGCCCT[C/T]GCACCCTCTGACCTA | 23352 |
rs2313510 | snp | C/T | 0 | 0 | intron-variant | UBR4 | GRCh38.p7 | 1:19199280 | GGGACCTGCAATCTT[C/T]TCAACTAGCACACTT | 23352 |
rs2872331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBR4 | GRCh38.p7 | 1:19114598 | TCTAGTTTCATTACC[A/G]ATCAACACTTTTCTA | 23352 |
rs3068081 | in-del | -/TTTTTT | | | intron-variant | UBR4 | GRCh38.p7 | 1:19185586 | ttctttttttttttt[-/TTTTTT]gagagggagtctcgc | 23352 |
rs3215751 | in-del | -/A | 0.00755907 | 0.0610114 | intron-variant | UBR4 | GRCh38.p7 | 1:19096230 | TTGTTGTTTTTAAAA[-/A]TGGATTTTGTAATGT | 23352 |
rs3737266 | snp | C/T | 0.0988009 | 0.199095 | intron-variant | UBR4 | GRCh38.p7 | 1:19153677 | TTTTATGGGCCTCCA[C/T]TGAAAGAGCTGGGAA | 23352 |
rs3748757 | snp | A/G | 0.457931 | 0.138798 | intron-variant | UBR4 | GRCh38.p7 | 1:19165363 | TTCCATTTTTCTCCC[A/G]TCTTGCCTCCCAGTG | 23352 |
rs3748758 | snp | G/T | 0.499396 | 0.0173617 | intron-variant | UBR4 | GRCh38.p7 | 1:19161999 | CGGGTCATTTGCGAG[G/T]CAACTATTCACCCCG | 23352 |
rs3748759 | snp | A/G | 0.499834 | 0.0091133 | intron-variant | UBR4 | GRCh38.p7 | 1:19161162 | CTTAGGGACTCTGAC[A/G]TTTTCTGTCCCTAGG | 23352 |
rs3748760 | snp | C/T | 0.0437281 | 0.141251 | downstream-variant-500B | UBR4 | GRCh38.p7 | 1:19074203 | GGCTGAAGGAAGGCT[C/T]GCGGAGTAGGGCACA | 23352 |
rs3748761 | snp | C/G | 0.477853 | 0.102875 | downstream-variant-500B | UBR4 | GRCh38.p7 | 1:19074197 | AGGAAGGCTCGCGGA[C/G]TAGGGCACAGTCTTG | 23352 |
rs3748762 | snp | A/G | 0.0908922 | 0.192833 | downstream-variant-500B | UBR4 | GRCh38.p7 | 1:19074132 | CTCATGCTGCTGTGA[A/G]TCGGGAATCCCTTGG | 23352 |
rs3762396 | snp | C/T | 0.458284 | 0.138267 | intron-variant | UBR4 | GRCh38.p7 | 1:19183900 | TTTTCTACTTGTCTT[C/T]AAGGTTCATCAGATG | 23352 |
rs3935168 | snp | C/G | | | intron-variant | UBR4 | GRCh38.p7 | 1:19166042 | TCTGCCAGTGATTTA[C/G]GGAAAAAGACACTTT | 23352 |
rs4066013 | snp | A/T | 0.40595 | 0.195396 | intron-variant | UBR4 | GRCh38.p7 | 1:19134141 | ctgggcatggtggca[A/T]gcacctagctactca | 23352 |
rs4319363 | snp | A/G | 0.0876345 | 0.190099 | intron-variant | UBR4 | GRCh38.p7 | 1:19132047 | TTACAACAGAATTTA[A/G]AAAATAATTTGAATT | 23352 |
rs4325153 | snp | A/C | 0.409552 | 0.192466 | intron-variant | UBR4 | GRCh38.p7 | 1:19166382 | AGTGAGCTCCTCTGT[A/C]CATCTCATCAGAGCT | 23352 |
rs4911974 | snp | C/T | 0.411242 | 0.191052 | intron-variant | UBR4 | GRCh38.p7 | 1:19116014 | TTGGAAAGATAAACC[C/T]AGGCTATTTTAGAGA | 23352 |
rs4911975 | snp | A/G | | | intron-variant | UBR4 | GRCh38.p7 | 1:19143263 | aaggaaggaaggaag[A/G]aagaaagaaagaaag | 23352 |
rs4911976 | snp | A/G | 0.260227 | 0.249791 | intron-variant | UBR4 | GRCh38.p7 | 1:19143295 | aagaaagaaagaaag[A/G]aagaaagaaagaaag | 23352 |
rs4911978 | snp | C/T | 0.432651 | 0.170701 | intron-variant | UBR4 | GRCh38.p7 | 1:19193052 | AAAGTACTGGGATCA[C/T]AGGTGTGAGTCACCA | 23352 |
rs4912045 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | UBR4 | GRCh38.p7 | 1:19094628 | TGAAATGAAAGGTTG[A/G]ACTAAAGCCTCTGTC | 23352 |
rs4912046 | snp | C/T | 0.477853 | 0.102875 | intron-variant | UBR4 | GRCh38.p7 | 1:19102435 | AAAGGTAAAGGTCCC[C/T]GACGAAGTCACAAAC | 23352 |
rs4912047 | snp | C/G | 0.193653 | 0.243567 | intron-variant | UBR4 | GRCh38.p7 | 1:19106128 | ATCTTCCTTAGCAAA[C/G]ATGCTGATCATTCTT | 23352 |
rs4912048 | snp | G/T | 0.409212 | 0.192748 | intron-variant | UBR4 | GRCh38.p7 | 1:19108938 | CCACTGTGGAAACAA[G/T]GATGGTCATATAGGG | 23352 |
rs4912049 | snp | A/G | | | intron-variant | UBR4 | GRCh38.p7 | 1:19143251 | caggaaggaaggaag[A/G]aaggaaggaagaaag | 23352 |
rs4912050 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | UBR4 | GRCh38.p7 | 1:19144168 | AACACTTTCCTTTCT[C/T]GGTCACTCACTCACA | 23352 |
rs4912051 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | UBR4 | GRCh38.p7 | 1:19188567 | taaaacaaaagagag[A/G]aaagaaaaTTACATT | 23352 |
rs4912054 | snp | A/G | 0.163892 | 0.234703 | intron-variant | UBR4 | GRCh38.p7 | 1:19197467 | AACCCCGACTCTACA[A/G]AAAATACAAAAATTA | 23352 |
rs5772831 | in-del | -/G | | | intron-variant | UBR4 | GRCh38.p7 | 1:19146517 | GCTTTAAAGCAACCA[-/G]GGGCCCAACCAAGCT | 23352 |
rs5772832 | in-del | -/T | | | intron-variant | UBR4 | GRCh38.p7 | 1:19185574 | CTGATTTCTTTTTTC[-/T]TTTTTTTTTTTTTTT | 23352 |
rs6426672 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | UBR4 | GRCh38.p7 | 1:19098915 | CCAATAGAAACaaga[A/G]aagggaagaaatggc | 23352 |
rs6426673 | snp | A/G | 0.111224 | 0.207945 | intron-variant | UBR4 | GRCh38.p7 | 1:19098969 | aagaaaaagaaacag[A/G]aagagaggaatggaa | 23352 |
rs6426677 | snp | A/G | 0.457325 | 0.1397 | synonymous-codon | UBR4 | GRCh38.p7 | 1:19106955 | CGTGGTGAGGGCCTC[A/G]ACGGGGACATCCTGG | 23352 |
rs6426678 | snp | C/T | 0.445987 | 0.155207 | intron-variant | UBR4 | GRCh38.p7 | 1:19121004 | TGGTATGAGAAGTCA[C/T]GCTGTTTAAGGTGTC | 23352 |