SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs2196 | snp | C/T | 0.442249 | 0.159814 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33914310 | TGAAAAAAGGGAAAA[C/T]ACCCATGTTTGCTAA | 54926 |
rs4817 | snp | C/T | 0.472147 | 0.114677 | utr-variant-3-prime | UBE2R2 | GRCh38.p7 | 9:33917500 | TCTTTTTTTAAAAAA[C/T]ATGAACCCAAACTCC | 54926 |
rs216364 | snp | C/T | 0.44546 | 0.155869 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33818259 | TGGAAAGAGCGGTGG[C/T]CTATCTGTGCTTTTT | 54926 |
rs216365 | snp | C/T | 0.0803491 | 0.183626 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33818743 | AGTCATGTAGGGAGA[C/T]TGATAGCTTCCTACT | 54926 |
rs216366 | snp | A/G | 0.157311 | 0.232183 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33819367 | AATATTCACTACTGT[A/G]TATAGTCACTGAGTA | 54926 |
rs216367 | snp | A/T | 0.472147 | 0.114677 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33819557 | ATTGCTGTGTTTATG[A/T]TGAAGCATATTCTCT | 54926 |
rs216368 | snp | A/G | 0.471483 | 0.115954 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33819957 | GCCTTTTCTGACAAA[A/G]CATTGTTTAGCAAAA | 54926 |
rs216369 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33820998 | GATAGTTTCTTCTGT[C/T]CATTCTGAATACTAT | 54926 |
rs216370 | snp | A/T | 0.356811 | 0.226034 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33822096 | CATATATATATATAt[A/T]ttttttttttttgag | 54926 |
rs216371 | snp | C/T | | | intron-variant | UBE2R2 | GRCh38.p7 | 9:33822201 | ggttcaagcgattct[C/T]ctgcctcagcctcct | 54926 |
rs471371 | snp | C/T | 0.44252 | 0.159487 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33870846 | CATTGTTCACTTATT[C/T]CCTCAATATAGAAAA | 54926 |
rs484194 | snp | G/T | 0.113334 | 0.209338 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33864519 | GGAGTAATTCCAGAA[G/T]AGTTGAAAAGGTTCA | 54926 |
rs568936 | snp | C/T | 0.15665 | 0.231917 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33846735 | tcattcatttataac[C/T]tatctgtggctgctt | 54926 |
rs574081 | snp | A/C | 0.0980852 | 0.198549 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33881084 | ttagaacacaaaatg[A/C]tgtaactaaaaactt | 54926 |
rs579004 | snp | A/G | 0.116838 | 0.211584 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33871152 | CTCTTTAAGCAACTA[A/G]TAGAGATTTCATTTG | 54926 |
rs733384 | snp | C/G | 0 | 0 | downstream-variant-500B | UBE2R2 | GRCh38.p7 | 9:33920453 | TAACAGTGATAATGA[C/G]ACCACCTTTTAGTTT | 54926 |
rs855719 | snp | C/T | 0.452719 | 0.146304 | utr-variant-5-prime | UBE2R2 | GRCh38.p7 | 9:33817619 | GTGTGGGGCCTGGTC[C/T]GGCCCGCCGGGTGTG | 54926 |
rs912732 | snp | C/T | 0.0760491 | 0.179558 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33852476 | AATCTGGCTAAGACT[C/T]CCACACATTGGCAGC | 54926 |
rs1041099 | snp | A/G | 0.3744 | 0.216852 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33899787 | ACTGGGGCTGGGCGC[A/G]GTGTCTCACGCCTGT | 54926 |
rs1044452 | snp | C/T | | | utr-variant-3-prime | UBE2R2 | GRCh38.p7 | 9:33917306 | GAGCAAGTGGGGACC[C/T]GGCCATGGCCCCTCA | 54926 |
rs1325105 | snp | A/C | 0.466824 | 0.124448 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33854962 | CACTTTGGGAGGCTA[A/C]GGTGGGTGGATCACT | 54926 |
rs1325106 | snp | C/T | 0 | 0 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33854898 | ATAGTGAAACTGCTT[C/T]TACAAAAAATAAAAA | 54926 |
rs1570777 | snp | C/T | 0.445196 | 0.1562 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33901237 | ataaccctagactaa[C/T]catgagaaaacacat | 54926 |
rs1570778 | snp | C/G | 0.0752113 | 0.178743 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33900933 | aaacagagagagaga[C/G]agagacagagacaga | 54926 |
rs1570779 | snp | C/G | 0.471863 | 0.115225 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33900621 | tatggacttcagtta[C/G]ttataatgaattaac | 54926 |
rs1570780 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33900584 | tattaactgcaacca[A/G]tgaatgacactaatg | 54926 |
rs1734666 | snp | G/T | | | intron-variant | UBE2R2 | GRCh38.p7 | 9:33818372 | TTTCTTTTTtggggg[G/T]gggggtgggggtggg | 54926 |
rs1749267 | snp | C/T | 0.157311 | 0.232183 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33846329 | taactcacgggaaaa[C/T]agtagcaaaaaatta | 54926 |
rs1749268 | snp | A/G | 0.442113 | 0.159977 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33837332 | atggtcggggctgag[A/G]taagaatatcgcttg | 54926 |
rs1749269 | snp | C/T | 0.471863 | 0.115225 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33836657 | tgattctcctgcctc[C/T]gcctcccgagtagct | 54926 |
rs1749270 | snp | A/C | 0.15698 | 0.23205 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33836439 | gtggtgatgattgca[A/C]aattctgactaaaaa | 54926 |
rs1749276 | snp | A/G | 0.114387 | 0.210022 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33879600 | ccaagcatggtggac[A/G]tgcctgtaatcccag | 54926 |
rs1749277 | snp | C/T | 0.155325 | 0.23138 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33866054 | acctgaggtcaggag[C/T]tcgagactagcctgg | 54926 |
rs1749278 | snp | C/T | 0.113685 | 0.209567 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33865579 | agtaatgagagaaat[C/T]ctcatcttccacagt | 54926 |
rs1769716 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33866430 | CCAACAAGGTGAAAC[C/T]CCGTCTCTACTAAAA | 54926 |
rs1769717 | snp | G/T | 0.155325 | 0.23138 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33866319 | cctgggaggtggagg[G/T]tgcagtgagctgaga | 54926 |
rs1769718 | snp | C/T | 0.442113 | 0.159977 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33866300 | AGTGAGCTGAGATCA[C/T]GCCACTGCACTCCAG | 54926 |
rs1769719 | snp | C/T | 0.155325 | 0.23138 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33866270 | gcctgggtgagggag[C/T]aagactctgtctcaa | 54926 |
rs1769721 | snp | C/T | 0.470811 | 0.117228 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33864066 | gctgaggcaaaagga[C/T]tgcttgcttgagacc | 54926 |
rs1769724 | snp | C/T | 0.442113 | 0.159977 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33836753 | tttttttttttgaga[C/T]aagagtcttgctctg | 54926 |
rs1769725 | snp | C/T | 0.471578 | 0.115772 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33870046 | gagactaggtttcac[C/T]atattggtcagtctg | 54926 |
rs1853760 | snp | C/T | 0.079617 | 0.182947 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33914360 | TCAAGCATTTGTAAT[C/T]CCCTTAACATGTCAT | 54926 |
rs1886585 | snp | C/T | 0.0752113 | 0.178743 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33904816 | TCTCCCCACCACCTC[C/T]AGCCCCACCAATTTA | 54926 |
rs1925235 | snp | C/T | 0.15698 | 0.23205 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33858365 | GAACCAAGTGCTTAA[C/T]AAAATACACTTATTG | 54926 |
rs2050789 | snp | C/T | 0.303938 | 0.244112 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33880692 | CAGGCCACAGAGTTG[C/T]ACCAGATCAGTATCG | 54926 |
rs2185321 | snp | C/T | | | intron-variant | UBE2R2 | GRCh38.p7 | 9:33840424 | TCTATCCCTTTTTTT[C/T]CCTTAGTTTTTATGT | 54926 |
rs2243565 | snp | C/T | 0.46875 | 0.121031 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33853411 | TCTGCCTCAGCCTCC[C/T]GAATAGCTGGGATTA | 54926 |
rs2243722 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33872576 | tggtcttgaccttct[A/G]acctcaggtgatttg | 54926 |
rs2244055 | snp | A/C | 0.113685 | 0.209567 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33869405 | TATACTTGGTTTTAC[A/C]TAGTTACATATACAA | 54926 |
rs2247487 | snp | C/T | 0.155325 | 0.23138 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33863072 | ACGCACCTGTAATCC[C/T]AGCTACTCAGGAGGC | 54926 |
rs2247503 | snp | C/T | 0.113685 | 0.209567 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33862788 | TAAACATTTCCCCCA[C/T]TTTGTGGTTTTGCCT | 54926 |
rs2248071 | snp | C/T | 0.466927 | 0.124269 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33857805 | TGACAGATTGTTGAA[C/T]GGCATGTGAACTGTT | 54926 |
rs2248085 | snp | C/G | 0.115438 | 0.210697 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33857596 | ggtcacggtggctca[C/G]gcctgtaatcccagc | 54926 |
rs2248910 | snp | C/T | 0.442385 | 0.15965 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33838477 | CATGGTAAACTTTCC[C/T]GAGATGTTTGCTAAT | 54926 |
rs2250083 | snp | C/T | 0.471196 | 0.1165 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33888755 | CCAAGGCAGGTGGAT[C/T]ACTTGGGGTCAGAAG | 54926 |
rs2250089 | snp | C/G | 0.0980852 | 0.198549 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33888572 | acccaggctggagtg[C/G]agtggtgcgatttca | 54926 |
rs2251015 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33876241 | gtggcatgcgcctgt[A/G]gctactcgagagact | 54926 |
rs2252125 | snp | A/G | 0.156319 | 0.231784 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33835199 | gttgcctaggctgga[A/G]tttaatggcatgatc | 54926 |
rs2252228 | snp | C/T | 0.0980852 | 0.198549 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33834111 | AATGTTTGGTAGACT[C/T]TAGAGTCCCACAGTA | 54926 |
rs2252367 | snp | A/C | 0.4711 | 0.116682 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33833001 | ATGGCTCTGAGGACT[A/C]AGAGTTATTATTTGT | 54926 |
rs2254030 | snp | A/T | 0.114036 | 0.209795 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33874373 | CTTCTTTTTTCAGTT[A/T]ATAAAAATAATAACA | 54926 |
rs2256180 | snp | C/T | 0.472052 | 0.11486 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33825231 | AAAAAGAATGATCTT[C/T]ATAAAAGCAAAGCTT | 54926 |
rs2256212 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33824326 | gtgaaacccggtctc[C/T]actaaaaatacacaa | 54926 |
rs2265039 | snp | C/G | 0.15698 | 0.23205 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33837650 | ggctgttcttgaact[C/G]ctgagctcaattgat | 54926 |
rs2265040 | snp | A/G | 0.441705 | 0.160466 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33844757 | caaggaaaaccactc[A/G]aaatcatttgccttt | 54926 |
rs2265539 | snp | A/G | 0.140242 | 0.224618 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33844813 | caccactacactcca[A/G]cctgggccacagagc | 54926 |
rs2265540 | snp | G/T | 0.0452528 | 0.143452 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33844577 | aattcagttcaacct[G/T]aaatggaatctgcta | 54926 |
rs2380872 | snp | A/G | 0.3742 | 0.216966 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33830653 | tgcgcctctcatccc[A/G]gccacttgggaggct | 54926 |
rs2477515 | snp | G/T | 0.115788 | 0.21092 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33831699 | GAGTCTCACTATGTC[G/T]CCCAGGCTGAAGTGC | 54926 |
rs2477516 | snp | A/G | 0.114738 | 0.210248 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33834814 | ACTCGGGAGGCTGAG[A/G]CAGGAGAATCCCTTG | 54926 |
rs2477517 | snp | A/G | 0.471578 | 0.115772 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33875960 | AAAATTTCAAAAAGG[A/G]AAGAAATTTCAGTGA | 54926 |
rs2486675 | snp | A/C | 0.471958 | 0.115042 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33845081 | acagttgattaaaaa[A/C]caaggcaatgaaggc | 54926 |
rs2486676 | snp | A/T | 0.5 | 0 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33859801 | CTCTCTCTCTCTCTC[A/T]CACACACACACACAC | 54926 |
rs2486677 | snp | C/T | 0.442249 | 0.159814 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33877852 | aagaCGgagggagag[C/T]gggagagagagagag | 54926 |
rs2486678 | snp | A/C/G | 0.0349115 | 0.127424 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33877823 | agagagagagagaga[A/C/G]agacagacagacaga | 54926 |
rs2734603 | snp | C/T | 0.0592351 | 0.161582 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33817966 | CCCGGACCCTGCTTC[C/T]GCGGCCGAGGCCTCC | 54926 |
rs2764317 | snp | C/G | | | intron-variant | UBE2R2 | GRCh38.p7 | 9:33877819 | agagagagagacaga[C/G]agacagacagacaga | 54926 |
rs2764318 | snp | G/T | 0.0984431 | 0.198823 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33874181 | gcaggcagatcactt[G/T]aagtcaggagttcaa | 54926 |
rs2764319 | snp | A/T | 0.0984431 | 0.198823 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33874180 | caggcagatcacttg[A/T]agtcaggagttcaac | 54926 |
rs2790726 | snp | A/C | 0.113685 | 0.209567 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33877715 | TGCCCTTAGATTATA[A/C]TACTACCAGCTTTAG | 54926 |
rs2790735 | snp | A/C | 0.0998734 | 0.199905 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33856871 | GAAAggaaggaagga[A/C]ggacggacagacgga | 54926 |
rs2790737 | snp | A/G | 0.0991586 | 0.199366 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33825492 | gcactttgggaggcc[A/G]aggtgggtggattac | 54926 |
rs2985703 | snp | C/T | 0.114738 | 0.210248 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33828722 | atgtgccaccatgcc[C/T]agctaatttttgtag | 54926 |
rs2994030 | snp | C/G | 0.494568 | 0.0518327 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33834925 | CAGGAAAAAAAAAAA[C/G]AAAAGAAAAGAAAAG | 54926 |
rs2994032 | snp | C/T | 0.442113 | 0.159977 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33824587 | gagcttgcagtgaac[C/T]gatatcgaggcactg | 54926 |
rs2994033 | snp | C/G | 0.442113 | 0.159977 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33824620 | CTCTAGCCTGGGCGA[C/G]AGAGCGAGGCTCTGT | 54926 |
rs3060448 | in-del | -/TT/TTG/TTT/TTTTG | 0 | 0 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33835165 | TTTTTTTTTTTTTTT[-/TT/TTG/TTT/TTTTG]GAGACCCAATCTCTT | 54926 |
rs3060468 | in-del | -/G/GTT | | | intron-variant | UBE2R2 | GRCh38.p7 | 9:33906138 | GTTGTTGTTGTTGTT[-/G/GTT]TTGAAATGGAGTTTT | 54926 |
rs3060472 | in-del | -/TAC | | | cds-indel | UBE2R2 | GRCh38.p7 | 9:33920355 | TTCTGCCCATCTGTC[-/TAC]TAATAAAATGTGAAA | 54926 |
rs3184789 | snp | A/C | | | utr-variant-3-prime | UBE2R2 | GRCh38.p7 | 9:33917407 | CTCCCTTTTTATGGG[A/C]CCTTTAATGGGAGAG | 54926 |
rs3814511 | snp | A/G | 0.331179 | 0.236453 | upstream-variant-2KB | UBE2R2 | GRCh38.p7 | 9:33816478 | GACAATAACAAACTG[A/G]GTCTCTAGCCCTTCT | 54926 |
rs3814512 | snp | C/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | UBE2R2 | GRCh38.p7 | 9:33816279 | TCTGAACCACGGGGG[C/G]ACCAAAGACTGTCCC | 54926 |
rs3824461 | snp | A/G | | | utr-variant-3-prime | UBE2R2 | GRCh38.p7 | 9:33917717 | TAAAAAAAAAAAAAA[A/G]CAAATTTGCCAAGGT | 54926 |
rs3832626 | in-del | -/CA | | | utr-variant-3-prime | UBE2R2 | GRCh38.p7 | 9:33917358 | GTGGGGAAACACACA[-/CA]GCTCCTGCTGACTCC | 54926 |
rs3849913 | snp | C/T | 0.331642 | 0.236293 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33870545 | TCACTCGTTCTCATA[C/T]TTCTTGGCTCCTCCC | 54926 |
rs3849914 | snp | C/T | 0.0752113 | 0.178743 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33871497 | TTTAGGGAGAACATA[C/T]GTGGTAATGGTACAG | 54926 |
rs4515641 | snp | A/G | 0.373799 | 0.217195 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33846424 | ttacattgtcattgc[A/G]taataaagacaatgc | 54926 |
rs4878551 | snp | C/G | 0.156319 | 0.231784 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33891540 | TAATCCCAGTTGCTT[C/G]GGAGGCTGAGGCATG | 54926 |
rs4878552 | snp | C/T | 0.4711 | 0.116682 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33896594 | actaccggcgctgtg[C/T]catgactggctattt | 54926 |
rs4879731 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | UBE2R2 | GRCh38.p7 | 9:33891462 | actagcctggccaac[A/T]cagtgaaatcccacc | 54926 |