SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs14170 | snp | C/T | 0.493744 | 0.0555782 | utr-variant-3-prime, synonymous-codon | AHSA2, USP34 | GRCh38.p7 | 2:61188357 | GGATTCTACCCTAGC[C/T]GAGGAAGAATCTGAG | 9736 |
rs16348 | in-del | -/CAAT | 0.5 | 0 | utr-variant-3-prime, intron-variant | AHSA2, USP34 | GRCh38.p7 | 2:61187505 | AAGTGCACAGAATAG[-/CAAT]CAATCAATCAGTCAT | 9736 |
rs751341 | snp | C/T | 0.498813 | 0.0243321 | intron-variant | USP34 | GRCh38.p7 | 2:61212071 | AGAAAGTTATAAAAT[C/T]AGTAACAAATTCTAT | 9736 |
rs777586 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | USP34 | GRCh38.p7 | 2:61201509 | ACTTTCTATAAGggc[C/T]ggacgtggtggctca | 9736 |
rs777587 | snp | C/T | 0.488545 | 0.074807 | intron-variant | USP34 | GRCh38.p7 | 2:61200540 | CTTTGTGGTAATTTT[C/T]ATATGGGCAACTGAG | 9736 |
rs777588 | snp | C/T | 0.474272 | 0.110462 | intron-variant | USP34 | GRCh38.p7 | 2:61199685 | GATAAAGATGACATC[C/T]CAAATTGGTGGGAAA | 9736 |
rs777589 | snp | A/G | 0.458315 | 0.13822 | intron-variant | USP34 | GRCh38.p7 | 2:61198486 | ATCTTATAATGGAGT[A/G]CTAGTCAAGAGTCCA | 9736 |
rs777590 | snp | C/G | 0.460027 | 0.135605 | intron-variant, utr-variant-3-prime | USP34, AHSA2 | GRCh38.p7 | 2:61190010 | CAAAAATATACCCAA[C/G]TAGAGATAAGACCAC | 9736 |
rs777591 | snp | A/G | 0.458951 | 0.137258 | intron-variant, utr-variant-3-prime | USP34, AHSA2 | GRCh38.p7 | 2:61190482 | AAGCATTAACTAATT[A/G]GAAATGACACACTGA | 9736 |
rs777592 | snp | C/G | 0.399253 | 0.200558 | intron-variant, downstream-variant-500B, utr-variant-3-prime | USP34, AHSA2 | GRCh38.p7 | 2:61191208 | TAATTATCTCACACA[C/G]AATCAGTGGTCTCAA | 9736 |
rs777593 | snp | A/C | 0.422473 | 0.180978 | intron-variant | USP34 | GRCh38.p7 | 2:61191968 | TACTGTAGAGAACAA[A/C]GTGGCATTTCTTCAG | 9736 |
rs778138 | snp | G/T | 0.380919 | 0.21298 | intron-variant | USP34 | GRCh38.p7 | 2:61460079 | CAACATAAAACTGTT[G/T]TCAAGTATCtttttt | 9736 |
rs778139 | snp | C/T | 0.470908 | 0.117046 | intron-variant | USP34 | GRCh38.p7 | 2:61457429 | AAGCTATAAGTAGGC[C/T]GTCTAGGTGTATATT | 9736 |
rs778140 | snp | A/G | 0.451732 | 0.147663 | intron-variant | USP34 | GRCh38.p7 | 2:61455841 | atattcttaatacat[A/G]tctcatagggatttt | 9736 |
rs778141 | snp | C/T | 0.451359 | 0.148171 | intron-variant | USP34 | GRCh38.p7 | 2:61455043 | aatacaaaaattagc[C/T]tagcattgtggcgtg | 9736 |
rs778142 | snp | A/C | 0.452473 | 0.146644 | intron-variant | USP34 | GRCh38.p7 | 2:61454293 | ctactaaaaacaaaa[A/C]ctagctgagcatgat | 9736 |
rs778143 | snp | G/T | 0.431029 | 0.17242 | intron-variant | USP34 | GRCh38.p7 | 2:61354755 | GGCTCCAGGCTTTCA[G/T]TTCCTCCACATGTTG | 9736 |
rs778144 | snp | A/C | 0.456332 | 0.141164 | intron-variant | USP34 | GRCh38.p7 | 2:61355993 | aatttaaattttaaa[A/C]aggttaccagaaaaa | 9736 |
rs778145 | snp | C/T | 0.484138 | 0.0876334 | intron-variant | USP34 | GRCh38.p7 | 2:61356500 | acacacacacacaca[C/T]acacacacacactgc | 9736 |
rs778146 | snp | A/G | 0.490063 | 0.0697833 | intron-variant | USP34 | GRCh38.p7 | 2:61379340 | cctggccaacacggt[A/G]aaaacccatctctac | 9736 |
rs778147 | snp | A/C | 0.421526 | 0.181876 | intron-variant | USP34 | GRCh38.p7 | 2:61379431 | aggctgaggcaagag[A/C]atcgcttgaacccag | 9736 |
rs778148 | snp | A/G | 0.436976 | 0.165952 | intron-variant | USP34 | GRCh38.p7 | 2:61379731 | AATACAGATTTTCAT[A/G]TTACTTTGTCCTATT | 9736 |
rs778149 | snp | A/T | 0.489893 | 0.0703642 | intron-variant | USP34 | GRCh38.p7 | 2:61381214 | tcaataaaaaaaaaa[A/T]aaataaataaataaa | 9736 |
rs778150 | snp | C/T | 0.484491 | 0.0866827 | intron-variant | USP34 | GRCh38.p7 | 2:61381237 | taaataaaaaataaa[C/T]aaaaaatgtaaaact | 9736 |
rs778151 | snp | A/C | 0.493837 | 0.055168 | intron-variant | USP34 | GRCh38.p7 | 2:61381285 | acacacacacacaca[A/C]aAAActacctagcta | 9736 |
rs778152 | snp | A/C | 0.456332 | 0.141164 | intron-variant | USP34 | GRCh38.p7 | 2:61381405 | gtgcaattgctcaat[A/C]agagctcactgcagc | 9736 |
rs778153 | snp | A/G | 0.490231 | 0.0692021 | intron-variant | USP34 | GRCh38.p7 | 2:61381517 | ctaattttcttctgc[A/G]cagagatggagtctc | 9736 |
rs778154 | snp | C/T | 0.435837 | 0.167226 | intron-variant | USP34 | GRCh38.p7 | 2:61419496 | TTGGTTAAAAATTCT[C/T]AATACAGGGATTAAA | 9736 |
rs778155 | snp | A/G | 0.460175 | 0.135375 | synonymous-codon | USP34 | GRCh38.p7 | 2:61420766 | TGTCCAGGAATTGAT[A/G]TAAGTAAATATTTTG | 9736 |
rs778156 | snp | A/G | 0.426035 | 0.177515 | intron-variant | USP34 | GRCh38.p7 | 2:61421797 | CACACACACACACAC[A/G]CGCGCGCGCGCGCAC | 9736 |
rs778157 | snp | C/G | 0.460365 | 0.13508 | intron-variant | USP34 | GRCh38.p7 | 2:61327154 | AGCATCCCAAAATTA[C/G]CTTCCCAAAATCGCA | 9736 |
rs778158 | snp | A/G | 0.459801 | 0.135955 | intron-variant | USP34 | GRCh38.p7 | 2:61328286 | CAGCCTGGGCAAAAG[A/G]GCAAAAACTCCGTCA | 9736 |
rs778159 | snp | C/T | 0.487495 | 0.0780784 | intron-variant | USP34 | GRCh38.p7 | 2:61329609 | TGAGTTCATAGACAG[C/T]CCAGAATACTAAGCT | 9736 |
rs778160 | snp | C/T | 0.378765 | 0.214288 | intron-variant | USP34 | GRCh38.p7 | 2:61330029 | CAAAAGTAGTGTTTG[C/T]GGAAATGTCAACTTG | 9736 |
rs796597 | snp | C/T | 0.443464 | 0.15834 | intron-variant | USP34 | GRCh38.p7 | 2:61453925 | ATGATGAAACCCTGT[C/T]TCTACCCAAAATACA | 9736 |
rs809011 | snp | A/C | 0.0372196 | 0.131242 | intron-variant | USP34 | GRCh38.p7 | 2:61329184 | GCGCCACCACGCCTG[A/C]CTTTTTTTTTTTTGT | 9736 |
rs810354 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | USP34 | GRCh38.p7 | 2:61202445 | AGCTCTCCTCCAGAG[A/G]TCCTCTATCTCGGGA | 9736 |
rs811372 | snp | C/T | 0.499995 | 0.00159744 | intron-variant | USP34 | GRCh38.p7 | 2:61202433 | GAACTCTGGAAGTCC[C/T]GAGATAGAGGACCTC | 9736 |
rs811378 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP34 | GRCh38.p7 | 2:61349382 | CATAATCAACAAGAT[A/G]TAAGTGGAGAAACCT | 9736 |
rs811871 | snp | C/T | 0.488606 | 0.0746142 | intron-variant | USP34 | GRCh38.p7 | 2:61350814 | TATTTTTTAATATGA[C/T]GGTAAAATGCTAATT | 9736 |
rs812925 | snp | C/G | 0.379158 | 0.214052 | intron-variant | USP34 | GRCh38.p7 | 2:61453858 | TAGTCTTTTGAATGT[C/G]ACACATATTTAACTA | 9736 |
rs921152 | snp | C/T | 0.489142 | 0.0728777 | intron-variant | USP34 | GRCh38.p7 | 2:61336140 | GTGTGTGTGTGTGTC[C/T]GCACAATTTTTTTTT | 9736 |
rs921153 | snp | A/G | 0.335559 | 0.234904 | intron-variant | USP34 | GRCh38.p7 | 2:61336273 | TGTAACTACAGGTAC[A/G]GGCCACCATGCCCAG | 9736 |
rs935861 | snp | C/T | 0.497121 | 0.0378299 | intron-variant | USP34 | GRCh38.p7 | 2:61251875 | CCTTGTTAGAAAGGC[C/T]GCCCCCTTGATATAC | 9736 |
rs935862 | snp | A/G | 0.415563 | 0.18732 | intron-variant | USP34 | GRCh38.p7 | 2:61251996 | GCAAACACACCCACA[A/G]CTTTTTCCATTCTGA | 9736 |
rs967968 | snp | C/G | 0.481242 | 0.0950111 | intron-variant | USP34 | GRCh38.p7 | 2:61428921 | CACAGAATTAGTCCA[C/G]ACAGGTAGCCAACAA | 9736 |
rs988911 | snp | A/G | 0.325004 | 0.238493 | intron-variant | USP34 | GRCh38.p7 | 2:61380375 | ACCTGAAATGATTCA[A/G]AAATAGAAAATACAC | 9736 |
rs1017584 | snp | C/T | 0.332337 | 0.236052 | intron-variant | USP34 | GRCh38.p7 | 2:61340771 | TGGGTTGTCTTACTA[C/T]TGAGTTATGAAATTA | 9736 |
rs1059541 | snp | C/G | 0.317451 | 0.240729 | utr-variant-3-prime, intron-variant | AHSA2, USP34 | GRCh38.p7 | 2:61187335 | AAGTCTGTGGGGACA[C/G]ATTAGTTCTGTGGAC | 9736 |
rs1059543 | snp | C/T | 0.3848 | 0.210544 | intron-variant | USP34 | GRCh38.p7 | 2:61193104 | TTTCCCCTTTATGTA[C/T]TTTAAAATATAGAAA | 9736 |
rs1137242 | snp | A/G | 0 | 0 | intron-variant | USP34 | GRCh38.p7 | 2:61359958 | gtttctactaaaaat[A/G]gaaaaattagcctgg | 9736 |
rs1186696 | snp | A/C | 0.480223 | 0.0974544 | intron-variant | USP34 | GRCh38.p7 | 2:61433348 | tccttacaagtggcg[A/C]atcggccaggtgcgg | 9736 |
rs1186697 | snp | A/G | 0.448452 | 0.152042 | intron-variant | USP34 | GRCh38.p7 | 2:61434282 | catccccccaggcca[A/G]ccaggcagccaagag | 9736 |
rs1186698 | snp | A/G | 0.204189 | 0.245767 | intron-variant | USP34 | GRCh38.p7 | 2:61434960 | gtacaagggaataca[A/G]gtaagaactttaatg | 9736 |
rs1186699 | snp | A/C | 0.401037 | 0.199218 | intron-variant | USP34 | GRCh38.p7 | 2:61435420 | cagaatccttacagg[A/C]aaggagtgaatggga | 9736 |
rs1186700 | snp | A/C | 0.45198 | 0.147323 | intron-variant | USP34 | GRCh38.p7 | 2:61436237 | tgggaatttgaggca[A/C]aagaatcgcttgaac | 9736 |
rs1186701 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | USP34 | GRCh38.p7 | 2:61437071 | gagggaagtttatag[C/T]aataaatgcctatgc | 9736 |
rs1186702 | snp | A/C | | | intron-variant | USP34 | GRCh38.p7 | 2:61437608 | gaaaccccgtctcta[A/C]taaaaatacaaaaaa | 9736 |
rs1186703 | snp | A/C | 0.460365 | 0.13508 | intron-variant | USP34 | GRCh38.p7 | 2:61445830 | ctatgcacatgtaat[A/C]ccagctactcgggag | 9736 |
rs1186704 | snp | A/G | 0.452597 | 0.146474 | intron-variant | USP34 | GRCh38.p7 | 2:61445856 | gggagcctgaggcag[A/G]agtatcgcttgaacc | 9736 |
rs1186705 | snp | A/C | 0.401392 | 0.198948 | intron-variant | USP34 | GRCh38.p7 | 2:61446143 | aaaaaaaCTAAACTA[A/C]AACTTAGAAATGTCT | 9736 |
rs1186706 | snp | G/T | 0.47934 | 0.0995154 | intron-variant | USP34 | GRCh38.p7 | 2:61446259 | ttttgaaaatctagg[G/T]tctagcttaatagaa | 9736 |
rs1186707 | snp | A/C | 0.476314 | 0.106217 | intron-variant | USP34 | GRCh38.p7 | 2:61446385 | gtaggaatattttaa[A/C]agctttgtcttaaat | 9736 |
rs1186708 | snp | A/G | 0.349233 | 0.229462 | intron-variant | USP34 | GRCh38.p7 | 2:61446571 | gaagccaaggcgggc[A/G]gatcacttaaagtca | 9736 |
rs1186709 | snp | C/T | 0.461148 | 0.133852 | intron-variant | USP34 | GRCh38.p7 | 2:61462245 | ctttttttttttttt[C/T]cccctgagatggagt | 9736 |
rs1186710 | snp | A/T | 0.481009 | 0.0955756 | intron-variant | USP34 | GRCh38.p7 | 2:61461592 | tgaggtgggaggatc[A/T]cttgagccctggaat | 9736 |
rs1186711 | snp | A/G | 0.437542 | 0.165312 | intron-variant | USP34 | GRCh38.p7 | 2:61461370 | atttcgctcttgttc[A/G]ctagggtggagtgca | 9736 |
rs1209434 | snp | A/G | 0.477768 | 0.103061 | intron-variant | USP34 | GRCh38.p7 | 2:61445823 | cgtggtgctatgcac[A/G]tgtaataccagctac | 9736 |
rs1211434 | snp | A/G | | | intron-variant | USP34 | GRCh38.p7 | 2:61437582 | ttcaagaccagcctg[A/G]ccaatatggtgaaac | 9736 |
rs1212149 | snp | G/T | 0 | 0 | intron-variant | USP34 | GRCh38.p7 | 2:61337307 | attgtgtttgtgaaa[G/T]tcaaccaagttgttc | 9736 |
rs1374659 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | USP34 | GRCh38.p7 | 2:61428636 | AAAGACAAAGCATAA[C/T]AATTACACAAGGATA | 9736 |
rs1376864 | snp | A/T | 0 | 0 | intron-variant | USP34 | GRCh38.p7 | 2:61332668 | TTATAGAAAGAGGCA[A/T]TGAAAAATGGCTCAC | 9736 |
rs1405490 | snp | C/T | 0.364401 | 0.222289 | intron-variant | USP34 | GRCh38.p7 | 2:61332945 | GGAGTATCACTTTTA[C/T]AGTTCTTGGAAGTCT | 9736 |
rs1465042 | snp | A/G | 0.459118 | 0.137002 | intron-variant | USP34 | GRCh38.p7 | 2:61345187 | TTTTGGGTTCAAGTG[A/G]TTCTCCTGCCTCAGC | 9736 |
rs1466034 | snp | A/C | 0 | 0 | intron-variant | USP34 | GRCh38.p7 | 2:61203058 | GAGAAAAATTATGAG[A/C]CAATCCTTTTTTTCT | 9736 |
rs1584300 | snp | A/C | 0.323434 | 0.238972 | intron-variant | USP34 | GRCh38.p7 | 2:61358866 | AGTAACACAATTTTC[A/C]AAAGCATGTAAAAGA | 9736 |
rs1584301 | snp | C/T | 0.346147 | 0.230772 | intron-variant | USP34 | GRCh38.p7 | 2:61358997 | ATTCATGTTAACGGA[C/T]AGGAAGACTTATTTT | 9736 |
rs1823685 | snp | C/T | 0.319616 | 0.240112 | intron-variant | USP34 | GRCh38.p7 | 2:61207950 | AACATGCCAAGAGTA[C/T]CATAAGAATTCACAG | 9736 |
rs1838978 | snp | C/T | 0.437118 | 0.165792 | intron-variant | USP34 | GRCh38.p7 | 2:61313788 | ATGGAAGCATGTTAT[C/T]TATAAGGAATGTATA | 9736 |
rs1867838 | snp | A/C | 0.472429 | 0.114129 | intron-variant | USP34 | GRCh38.p7 | 2:61467696 | GTAGGCGGAGGTTGC[A/C]GTGAGCCGAGATCAT | 9736 |
rs1867839 | snp | A/C | 0.471292 | 0.116318 | intron-variant | USP34 | GRCh38.p7 | 2:61467662 | ACTGCACTCCAGCCT[A/C]GGCCACAGAACAAGA | 9736 |
rs1880866 | snp | C/G | 0.485664 | 0.0834419 | upstream-variant-2KB, nc-transcript-variant | USP34, LOC105377633 | GRCh38.p7 | 2:61471837 | CCTCTTCCGTAAAAA[C/G]GAGACGATGTCAGGC | 9736 |
rs1900572 | snp | G/T | 0.468949 | 0.12067 | | | GRCh38.p7 | 2:61423580 | aaatcccacattcac[G/T]ggttggaagacatta | 9736 |
rs1900573 | snp | C/T | 0.388964 | 0.20782 | | | GRCh38.p7 | 2:61369777 | agaaaaaaaaaaaag[C/T]caaagccacatctgg | 9736 |
rs2005285 | snp | C/T | 0.4941 | 0.0539917 | intron-variant | USP34 | GRCh38.p7 | 2:61253955 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 9736 |
rs2034311 | snp | A/T | 0.314544 | 0.241524 | intron-variant | USP34 | GRCh38.p7 | 2:61396413 | TGTGGGTTAATGAGC[A/T]TCGTTATGCGTATAT | 9736 |
rs2053750 | snp | A/T | 0.477684 | 0.103247 | intron-variant | USP34 | GRCh38.p7 | 2:61429138 | agacactatctctac[A/T]aaacaaattttaaaa | 9736 |
rs2060824 | snp | C/T | 0.499759 | 0.0109798 | intron-variant | USP34 | GRCh38.p7 | 2:61257421 | GTTCTTCAATGAACA[C/T]ATAACAAAAACAAAA | 9736 |
rs2060825 | snp | A/G | 0.25045 | 0.25 | intron-variant | USP34 | GRCh38.p7 | 2:61263639 | GGTACCCACCACCAT[A/G]CCCAGCTATTTTTTT | 9736 |
rs2067548 | snp | C/T | 0.172674 | 0.237741 | intron-variant | USP34 | GRCh38.p7 | 2:61288446 | GTGAGACTGAATTTA[C/T]TATTTGAACTCAGTA | 9736 |
rs2067549 | snp | C/G | 0.250732 | 0.249999 | intron-variant | USP34 | GRCh38.p7 | 2:61288270 | GGAGCCATTTATCAC[C/G]CCTAGATCTTGTGGA | 9736 |
rs2084318 | snp | C/T | 0.488057 | 0.0763479 | intron-variant | USP34 | GRCh38.p7 | 2:61425466 | gggacaacacagcaa[C/T]tgcaagccactgaac | 9736 |
rs2100123 | snp | A/T | 0.320814 | 0.239761 | intron-variant | USP34 | GRCh38.p7 | 2:61425211 | GGATACCAAATTAAG[A/T]TCTACATAGAAAAAA | 9736 |
rs2121660 | snp | C/T | 0.445592 | 0.155704 | intron-variant | USP34 | GRCh38.p7 | 2:61425923 | ggactctcttgcatc[C/T]tggataccagctcag | 9736 |
rs2121661 | snp | A/G | 0.463126 | 0.13068 | intron-variant | USP34 | GRCh38.p7 | 2:61334523 | TGCATGAGCCTTAAA[A/G]GAGGCAAAACAAATT | 9736 |
rs2121663 | snp | A/G | 0 | 0 | intron-variant | USP34 | GRCh38.p7 | 2:61361062 | tcttgagtaagaata[A/G]agttggaagtatcac | 9736 |
rs2123111 | snp | C/T | 0.491394 | 0.0650306 | intron-variant | USP34 | GRCh38.p7 | 2:61223319 | AGGAAGAAAAACTTA[C/T]TTCCACTAATATTTT | 9736 |
rs2123112 | snp | A/C | 0.476918 | 0.104919 | intron-variant | USP34 | GRCh38.p7 | 2:61214940 | AGGCAAGCTAAAGAA[A/C]AGTGGTTTAAAAATT | 9736 |
rs2123113 | snp | C/G | 0.321053 | 0.23969 | intron-variant | USP34 | GRCh38.p7 | 2:61290336 | GCAATTTCATCACTT[C/G]GTATTAATCCAAGAG | 9736 |
rs2166720 | snp | C/T | 0.326605 | 0.237974 | synonymous-codon | USP34 | GRCh38.p7 | 2:61350300 | AGTATTTAATAAAGA[C/T]GCAAAAGAACTCTGT | 9736 |