SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs751584386 | snp | C/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132662263 | TATATGGAATTTTAA[C/T]AAAGTTCAGCTTTAA | 79876 |
rs751616849 | snp | A/G | 3.31345e-05 | 0.00407016 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132676523 | CAAAATGAAGAATAT[A/G]TAGATAATGGACTGG | 79876 |
rs751709115 | snp | A/C | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132663996 | AGAGAATAGAGCAGA[A/C]AACTAAAATAGTAGA | 79876 |
rs751820042 | snp | A/G | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132663689 | AGTCAAACAGTTATT[A/G]CCTATATTGTTACCT | 79876 |
rs751933522 | snp | A/G | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132674145 | GGGTAAAAAACAGGC[A/G]TTTAATTTTTCTTTT | 79876 |
rs751998415 | snp | A/T | 9.93443e-05 | 0.00704715 | missense, intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675377 | GAAGCAGCAGGAGGA[A/T]TATAAGGTATATGAC | 79876 |
rs752006386 | in-del | -/TT | 1.65633e-05 | 0.00287774 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132665937 | ACTTCTGGTGACATA[-/TT]TGATGAAGAGCTATT | 79876 |
rs752029753 | snp | A/G | | | intron-variant | ACAD11, UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132657347 | TCTGTCTATCTCTGT[A/G]CTAATATCATACCAT | 79876 |
rs752077195 | snp | A/G | 1.65759e-05 | 0.00287883 | synonymous-codon, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675652 | TATACAAGAAGAGGA[A/G]GAGATAATCCATGAA | 79876 |
rs752164143 | in-del | -/ATAAAT | 1.67725e-05 | 0.00289585 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132672227 | ATGCTTTCAGTAAAC[-/ATAAAT]ATATTTCACAAAGCA | 79876 |
rs752171911 | snp | G/T | 1.65638e-05 | 0.00287778 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132665883 | GGTATGATAAACCCT[G/T]TCCAAGTTTTTGTAA | 79876 |
rs752187780 | snp | G/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132669409 | GTAGCTAGGACTACA[G/T]GCACGTGCCACCATG | 79876 |
rs752287654 | snp | C/T | | | intron-variant, utr-variant-5-prime | ACAD11, UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132654554 | ATGTCTGTGGAGAGC[C/T]GTAAAAGCCAATCAT | 79876 |
rs752452687 | snp | A/G | 1.67525e-05 | 0.00289413 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132672032 | TTTTTTTTGAAATGT[A/G]TTTTATTTTTCATGT | 79876 |
rs752457127 | in-del | -/CT | 5.14223e-05 | 0.00507035 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132666111 | TCATATAGGGAACTA[-/CT]CTCACTCCTGGAGTA | 79876 |
rs752461514 | snp | C/G | 1.64819e-05 | 0.00287066 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132671811 | AAACATGGATGGAAT[C/G]TGGGGTCAGTGAAAA | 79876 |
rs752479463 | snp | C/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132662714 | ATGTGTTATGGAATA[C/T]AGTTATAAGCATGTG | 79876 |
rs752538357 | snp | C/T | 1.6996e-05 | 0.00291508 | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132659757 | CTGGCTTCATGATCA[C/T]CCCCGCAGGCCACAG | 79876 |
rs752553531 | snp | A/G | 1.64887e-05 | 0.00287125 | upstream-variant-2KB, utr-variant-5-prime, missense, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132659658 | CAAAGCCAGACAAGT[A/G]CTGGTTTAGGTAGGC | 79876 |
rs752743266 | in-del | -/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132667994 | TAGGTTAATTTTTTT[-/T]CTTTTTAGTTTTTTA | 79876 |
rs752886771 | snp | C/T | 3.34694e-05 | 0.00409067 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132668945 | AAATGGAATAGCAAT[C/T]AAGTACCATATTCAG | 79876 |
rs752938981 | in-del | -/T | 1.66871e-05 | 0.00288847 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675580 | AATGAGTAAGAACAC[-/T]TTTGATGCTGTTTGA | 79876 |
rs752969077 | snp | C/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132674385 | TTACTTTTGCGCCAA[C/T]CTAATAAAAGACATC | 79876 |
rs753148999 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132658859 | CATTAATAAGACTAA[C/T]CAAAATAGGTATTAC | 79876 |
rs753235048 | snp | A/C | 4.72244e-05 | 0.00485901 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675222 | GTTTTAAATTTCTTT[A/C]TTTAAGTCTATTTTG | 79876 |
rs753304973 | snp | C/T | 1.68417e-05 | 0.00290182 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132665776 | TATTTGTATTACTAA[C/T]ACCTAAAAGACTGTA | 79876 |
rs753315973 | snp | A/T | 8.31566e-05 | 0.00644759 | upstream-variant-2KB, utr-variant-5-prime, missense, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132660664 | GTCCGCATCGAGAAG[A/T]TGAGCTCAGAGGTGG | 79876 |
rs753324669 | snp | A/C | 3.30983e-05 | 0.00406793 | missense, intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675366 | AGAAATTGCAGGAAG[A/C]AGCAGGAGGAATATA | 79876 |
rs753493645 | snp | A/G | 1.65515e-05 | 0.00287671 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132665866 | ATTGTAAGCGACTAT[A/G]AGGTATGATAAACCC | 79876 |
rs753687713 | snp | A/G/T | 6.60005e-05 | 0.00574426 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132671041 | GAAGCTCGAATGACA[A/G/T]TAAATACAGTGAGTA | 79876 |
rs753792163 | snp | A/T | 1.65282e-05 | 0.00287469 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132659561 | AAGGAAAACTCAATG[A/T]ACAAATTTTTTTCCG | 79876 |
rs753888009 | snp | A/G | 1.6489e-05 | 0.00287128 | upstream-variant-2KB, utr-variant-5-prime, synonymous-codon, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132659644 | CTCACGTTCGGCCCC[A/G]AAGCCAGACAAGTGC | 79876 |
rs754036932 | snp | C/G | 1.69146e-05 | 0.0029081 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675836 | TGAGCTGGTATCTGA[C/G]GTTTCAGAAGAGGAA | 79876 |
rs754096555 | snp | C/G | | | downstream-variant-500B, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132678213 | TTTTTTGTCTAATAT[C/G]TTTCATTAAAAACAA | 79876 |
rs754124787 | snp | A/T | 2.06597e-05 | 0.00321394 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675942 | CTTCAAAAATATGAT[A/T]TACCCATATGTAAAT | 79876 |
rs754140626 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132658974 | TAGGACTCTTTCTGT[A/G]GCCCTGTATTAGTAA | 79876 |
rs754212715 | snp | C/T | 1.65932e-05 | 0.00288034 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132668921 | AAGCAGCAGAACATA[C/T]TCTGAGGTAAATGGA | 79876 |
rs754428068 | snp | A/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132668031 | AGAAAATCCCATTTT[A/T]GTTTTTATTGTTTAG | 79876 |
rs754466338 | snp | A/C | 1.68485e-05 | 0.00290241 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132665778 | TTTGTATTACTAATA[A/C]CTAAAAGACTGTAAG | 79876 |
rs754550589 | snp | G/T | | | intron-variant, upstream-variant-2KB | ACAD11, UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132652792 | CAAAGTCCCTTAGAG[G/T]GTAGCTTCAGCCTGA | 79876 |
rs754585015 | snp | G/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132673517 | AATGCCTGGCTAATT[G/T]TTGTATTTTTTGTAG | 79876 |
rs754846540 | snp | A/C | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132661010 | AAGACTGATAGTAAG[A/C]ACTTTCAGAAGATGA | 79876 |
rs754852475 | snp | A/T | 1.65222e-05 | 0.00287417 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132671770 | GTTTTCACCCATTTC[A/T]ACTAAGGCTTGTAAT | 79876 |
rs754872249 | snp | A/G | 1.65274e-05 | 0.00287462 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132659562 | AGGAAAACTCAATGT[A/G]CAAATTTTTTTCCGC | 79876 |
rs754965052 | snp | A/G | 1.64885e-05 | 0.00287123 | upstream-variant-2KB, utr-variant-5-prime, missense, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132659646 | CACGTTCGGCCCCAA[A/G]GCCAGACAAGTGCTG | 79876 |
rs755019454 | snp | G/T | 1.67573e-05 | 0.00289454 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675686 | AATGAATGGGGTAGG[G/T]ATTCTTTTATAAATT | 79876 |
rs755085235 | snp | C/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132663694 | AACAGTTATTGCCTA[C/T]ATTGTTACCTTTATT | 79876 |
rs755105199 | snp | A/G | 1.65408e-05 | 0.00287578 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132665973 | AACATATACTATTTT[A/G]TATTTCACAGAAAAT | 79876 |
rs755107477 | snp | A/G | 1.68142e-05 | 0.00289945 | synonymous-codon, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675851 | GGTTTCAGAAGAGGA[A/G]CTGAAAAATTTTTCA | 79876 |
rs755191037 | in-del | -/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132664568 | TGTTAAAGCAAATTG[-/T]TTGGACTCCACATTC | 79876 |
rs755356052 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132659250 | AATTACACCAGCTTC[C/T]CAGAAAAAGATCTAA | 79876 |
rs755378234 | snp | A/G | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132674169 | TTCTTTTTATTTGTG[A/G]AAAAGGTTGAACACT | 79876 |
rs755453105 | snp | A/C | 1.65395e-05 | 0.00287567 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132672077 | CTTGTAGTTGCTGCA[A/C]ATATTGATGAAAAGA | 79876 |
rs755535417 | snp | A/C | 0.00012851 | 0.00801489 | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132660525 | GGGAGCGTTGGCGGC[A/C]GGAGTCCCAGCCATG | 79876 |
rs755595366 | snp | A/G | | | intron-variant, utr-variant-5-prime | ACAD11, UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132654555 | TGTCTGTGGAGAGCC[A/G]TAAAAGCCAATCATG | 79876 |
rs755608181 | snp | A/G | 1.66918e-05 | 0.00288888 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132672212 | TCTGAATAGTCTTGT[A/G]TGCTTTCAGTAAACA | 79876 |
rs755696045 | snp | C/T | 5.06693e-05 | 0.0050331 | upstream-variant-2KB, utr-variant-5-prime, missense, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132660652 | GGGGGCGGCCGGGTC[C/T]GCATCGAGAAGATGA | 79876 |
rs755718719 | in-del | -/AAGTA | 1.6507e-05 | 0.00287284 | frameshift-variant, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132668895 | TCATCAAGCAGGATT[-/AAGTA]AAGTTCAAGCAGCAG | 79876 |
rs755806234 | in-del | -/A | 1.65596e-05 | 0.00287741 | frameshift-variant, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675626 | GTAGCAGCACTGCCT[-/A]AACAAGAGGTTATAC | 79876 |
rs755808623 | snp | C/G | 3.34767e-05 | 0.00409112 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132676420 | GGTTCTTTTTTCACT[C/G]TATTTCCCTTATTTG | 79876 |
rs756026783 | snp | G/T | 1.65616e-05 | 0.00287759 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132670928 | TTAGAGTGTATTTTG[G/T]GTCCTGATGTTTTTC | 79876 |
rs756289017 | snp | C/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132673060 | TTGCGAGCAAAGAAA[C/T]TGAAAAAAGCATACA | 79876 |
rs756301582 | snp | A/C | 0.000127482 | 0.00798278 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132670283 | TTCATGGATAGAATA[A/C]GGTAAAATTTTAATT | 79876 |
rs756336575 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132659536 | TTAGGAAACCACCCA[A/G]GGCCAAAGGAAGGAA | 79876 |
rs756337960 | snp | G/T | 1.6674e-05 | 0.00288734 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675677 | CATGAAGATAATGAA[G/T]GGGGTAGGTATTCTT | 79876 |
rs756360659 | snp | C/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132674462 | GGAGGCCAAGGCAGG[C/T]GGATTGCTTGAGCCC | 79876 |
rs756448688 | snp | A/G | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132676058 | TAAGATGTGAGAGAG[A/G]GGTATGCAGTGTTAA | 79876 |
rs756461216 | snp | C/G | 4.96923e-05 | 0.00498434 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132665946 | GACATATTTGATGAA[C/G]AGCTATTAACCAACA | 79876 |
rs756520407 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132658891 | ACTTAGGAAACTAGT[C/T]CTCAGAGTGTTTATG | 79876 |
rs756713587 | snp | A/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132666572 | TACCAGAATTCAGTC[A/T]ACCAATCTTAGATTT | 79876 |
rs756719767 | snp | A/G | 3.29908e-05 | 0.00406132 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132671870 | ATTCCTGGAGAATCT[A/G]CTTGTTTTGCGGTAT | 79876 |
rs756799117 | in-del | -/T | 6.74929e-05 | 0.00580878 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132676409 | AATTCTATATGGTTC[-/T]TTTTTTCACTGTATT | 79876 |
rs756815658 | snp | C/T | 1.65666e-05 | 0.00287802 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132672057 | TCATGTAGTGTGCTC[C/T]ACCACTTGTAGTTGC | 79876 |
rs756905752 | snp | A/G | 1.76288e-05 | 0.00296885 | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132659799 | CCACAGGTCTCGAGT[A/G]CCGAAGTCCTTCAGG | 79876 |
rs757035355 | snp | A/G | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132664487 | TAACCACAGCAAGAG[A/G]GTAAGTTTAAAAATA | 79876 |
rs757180098 | snp | C/G | 1.69143e-05 | 0.00290807 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132676399 | TAAGCATCAAGAATT[C/G]TATATGGTTCTTTTT | 79876 |
rs757242211 | snp | G/T | 1.66032e-05 | 0.0028812 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132670914 | GTAAGTATAATGTAT[G/T]AGAGTGTATTTTGTG | 79876 |
rs757358257 | snp | C/T | | | intron-variant | ACAD11, UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132654896 | TTAGCATAAATAGGC[C/T]GATTTGAACCCGATA | 79876 |
rs757374363 | snp | C/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132676400 | AAGCATCAAGAATTC[C/T]ATATGGTTCTTTTTT | 79876 |
rs757478430 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132660287 | GCGAGGAAGGAAGCC[G/T]AAAGAGCCAGGTTTT | 79876 |
rs757746106 | snp | A/C | 1.67503e-05 | 0.00289393 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132665799 | AGACTGTAAGCTTTA[A/C]AACATATTTTTCTTT | 79876 |
rs757775810 | in-del | -/CTCA | | | intron-variant, nc-transcript-variant | NPHP3-ACAD11, UBA5 | GRCh38.p7 | 3:132678678 | TTTTTGAGACAGAGT[-/CTCA]CTCTGTTGCCCAGGC | 79876 |
rs757825403 | snp | G/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132669715 | CACCAATCCCTGCTT[G/T]AGGAATTTCCTTTGT | 79876 |
rs757837845 | snp | A/C | 3.31378e-05 | 0.00407036 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132665887 | TGATAAACCCTTTCC[A/C]AGTTTTTGTAAGATT | 79876 |
rs757845310 | snp | A/G | | | intron-variant, upstream-variant-2KB | ACAD11, UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132653334 | AGCAATCAGATGAGA[A/G]CTTCCACAAGCTTAC | 79876 |
rs758058913 | snp | C/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132666205 | CTAGATTGTTCTTTC[C/T]ACTCGGGTTGAGACA | 79876 |
rs758129447 | snp | A/G | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132667805 | AGTTTAATGTTTCCC[A/G]CAACTTATGTATAAA | 79876 |
rs758240623 | snp | C/T | | | intron-variant, upstream-variant-2KB | ACAD11, UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132652509 | TATACTTCACTTGCC[C/T]TTTCCTCACTTCATG | 79876 |
rs758333344 | snp | G/T | 3.3006e-05 | 0.00406226 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132659588 | TCCGCTGGAGGCAAA[G/T]GCTGACATCCATACC | 79876 |
rs758372365 | snp | A/C/G | 0.000184697 | 0.00960814 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675858 | GAAGAGGAACTGAAA[A/C/G]ATTTTTCAGGTCCAG | 79876 |
rs758456571 | snp | C/T | 5.04655e-05 | 0.00502297 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132668957 | AATCAAGTACCATAT[C/T]CAGTGAAATCTTACT | 79876 |
rs758644249 | in-del | -/G | | | upstream-variant-2KB, intron-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132658972 | GATAGGACTCTTTCT[-/G]TAGCCCTGTATTAGT | 79876 |
rs758834494 | snp | C/T | | | intron-variant, utr-variant-5-prime | ACAD11, UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132654616 | AGAACTCTGAGGCCT[C/T]CTTTCCTTTGGCTGT | 79876 |
rs758836261 | snp | A/C/T | 1.68627e-05 | 0.00290363 | upstream-variant-2KB, utr-variant-5-prime, missense, synonymous-codon, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132660669 | CATCGAGAAGATGAG[A/C/T]TCAGAGGTGGTGGAT | 79876 |
rs758892805 | snp | A/T | 2.3248e-05 | 0.00340932 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675223 | TTTTAAATTTCTTTA[A/T]TTAAGTCTATTTTGA | 79876 |
rs758963280 | snp | A/T | | | intron-variant | ACAD11, UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132655520 | CCAGGGCCTTTGCAT[A/T]AGCAGTCCCCTCTGT | 79876 |
rs758979156 | snp | A/G | 1.65537e-05 | 0.0028769 | missense, intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675372 | TGCAGGAAGCAGCAG[A/G]AGGAATATAAGGTAT | 79876 |
rs759071206 | snp | C/G | 6.62394e-05 | 0.00575459 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675635 | CTGCCTAAACAAGAG[C/G]TTATACAAGAAGAGG | 79876 |
rs759157155 | snp | A/C | 6.62054e-05 | 0.00575312 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132665874 | CGACTATGAGGTATG[A/C]TAAACCCTTTCCAAG | 79876 |
rs759157820 | snp | A/G | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132669360 | GCACCTCCGCCTCCC[A/G]GGCTCAAGCTATCTT | 79876 |
rs759161287 | snp | A/G | 3.73009e-05 | 0.00431846 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675777 | GAATAATTATTGCTT[A/G]TTAAATTCCTTAAAA | 79876 |
rs759166541 | snp | G/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132671533 | ACATTAATTTGACAA[G/T]AAATCCAATAAACTT | 79876 |
rs759237730 | in-del | -/G | | | intron-variant | ACAD11, UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132655428 | CTTTATTGCCTGACA[-/G]GGTCCCTGTTGCCCT | 79876 |
rs759250524 | snp | A/G | 3.3012e-05 | 0.00406262 | synonymous-codon, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132666013 | TGCCGTAGCAATAGT[A/G]GGTGTTGGTGGAGTA | 79876 |
rs759310417 | snp | A/G | | | utr-variant-5-prime, missense, intron-variant, upstream-variant-2KB | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132661032 | AGAAGATGAGATCAA[A/G]TATTAAACCTGCTAA | 79876 |
rs759346805 | snp | C/T | | | intron-variant | ACAD11, UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132657423 | CTATCCTTAGCCCTT[C/T]GCTCTTACACATAAA | 79876 |
rs759388024 | snp | C/G | 1.67699e-05 | 0.00289563 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132672030 | CTTTTTTTTTGAAAT[C/G]TGTTTTATTTTTCAT | 79876 |
rs759446670 | snp | C/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675545 | TGTCTGAATTCTTGA[C/T]TAATGCTTTAGAGAA | 79876 |
rs759558005 | in-del | -/AA | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132673608 | CCACCTCAGCCTCCC[-/AA]AGTGTTGGGATTACA | 79876 |
rs759606290 | snp | C/G | 1.6531e-05 | 0.00287493 | synonymous-codon, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132672121 | AGGTGTTTGTGCAGC[C/G]AGTCTTCCTACCACT | 79876 |
rs759636072 | snp | C/T | 1.65883e-05 | 0.00287991 | upstream-variant-2KB, utr-variant-5-prime, missense, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132659724 | GCACTTCGGCCAAAT[C/T]GGACTCGCCAGTAGC | 79876 |
rs759693805 | snp | A/G | 0.000108927 | 0.00737912 | upstream-variant-2KB, utr-variant-5-prime, synonymous-codon, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132660570 | GCGCCTGCAGCAGCG[A/G]GTCCAGGAGCTGGAG | 79876 |
rs759758677 | snp | C/T | 2.13751e-05 | 0.00326911 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675943 | TTCAAAAATATGATT[C/T]ACCCATATGTAAATA | 79876 |
rs759822455 | snp | C/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132667305 | AATGCAGCTAGACCA[C/T]GCCATTTTGAGTAGC | 79876 |
rs759846456 | snp | C/G | 1.66032e-05 | 0.0028812 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132668923 | GCAGCAGAACATACT[C/G]TGAGGTAAATGGAAT | 79876 |
rs759846536 | snp | A/G | 1.65239e-05 | 0.00287431 | synonymous-codon, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132676493 | TTCTGGTGAAAGCTT[A/G]GAAGACCTCATGGCC | 79876 |
rs759934449 | snp | A/C | 2.59872e-05 | 0.00360457 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132670262 | ACAGTGGAAAACTTT[A/C]AACATTTCATGGATA | 79876 |
rs760024033 | snp | A/T | 1.65141e-05 | 0.00287346 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132670956 | TTCAAACTTATTTTC[A/T]TTGACTAGTAATGGT | 79876 |
rs760111062 | in-del | -/TTTC | 0.000122901 | 0.00783809 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675215 | TTTTCATGTTTTAAA[-/TTTC]TTTATTTAAGTCTAT | 79876 |
rs760137778 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132677414 | CAAGGTTTGTCCTGT[A/G]TATTAGGAATAAAGG | 79876 |
rs760150546 | snp | A/G | 6.61594e-05 | 0.00575112 | missense, intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675348 | AATCCTCAGTGTGAT[A/G]ACAGAAATTGCAGGA | 79876 |
rs760154860 | snp | A/G | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132671922 | TCTTCACTGTTAGAT[A/G]CTTGAGTTCTTAGGG | 79876 |
rs760332635 | snp | A/G/T | | | intron-variant | ACAD11, UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132656683 | ATTTTTAGTAGAGAC[A/G/T]GGGTTTCACCATGTT | 79876 |
rs760372318 | snp | C/G | 1.65674e-05 | 0.00287809 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675614 | CTACAGAAAAAGGTA[C/G]CAGCACTGCCTAAAC | 79876 |
rs760442979 | snp | A/G | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132665512 | ATATTCTACCAAAGC[A/G]TAGAAAAATGTTGAA | 79876 |
rs760459551 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132658115 | TGATCCACGTGCCTC[A/G]GCCTCCCAAAGTGCT | 79876 |
rs760603622 | in-del | -/TCTAG | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132659939 | TCCCGAGGTTTTAGC[-/TCTAG]TCAAGTGCCAAAAGA | 79876 |
rs760638837 | snp | C/G | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132667249 | TGCATATTAAAGTTG[C/G]AGAAGTGCTCTTGCA | 79876 |
rs760720892 | snp | C/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132665641 | CTTGGGAGAGTTTTT[C/T]TAAACGGTGCCTGGG | 79876 |
rs760787432 | snp | A/T | 6.65292e-05 | 0.00576716 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132671753 | TTATTTTTTTTCCTT[A/T]TGTTTTCACCCATTT | 79876 |
rs760879507 | snp | C/T | 5.63227e-05 | 0.00530643 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132672016 | CTCATACTTTTTCTC[C/T]TTTTTTTTGAAATGT | 79876 |
rs760969249 | snp | A/G | 8.25512e-05 | 0.00642408 | upstream-variant-2KB, utr-variant-5-prime, stop-gained, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132659703 | TGTCGAACTTGTGCT[A/G]GGGCAGCACTTCGGC | 79876 |
rs760984777 | snp | C/T | 1.73027e-05 | 0.00294127 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675814 | ATAGGATCAAATTTA[C/T]AGGTATTGAGCTGGT | 79876 |
rs761013116 | snp | G/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675104 | AAATAAGATAAAATT[G/T]CTGTTTTCTGGATGC | 79876 |
rs761074855 | snp | A/T | 1.76456e-05 | 0.00297026 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675922 | ACACAATTCCAAAAA[A/T]GGTACTTCAAAAATA | 79876 |
rs761169562 | snp | A/G | 2.47957e-05 | 0.00352097 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132670250 | TATAATATAACCACA[A/G]TGGAAAACTTTCAAC | 79876 |
rs761177005 | snp | A/G | | | intron-variant, upstream-variant-2KB | ACAD11, UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132653101 | GACAAAGCATTAGTA[A/G]TATCTACTGAAATAT | 79876 |
rs761221286 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132660217 | CAACATCGCTGGCCT[C/T]CTGCCCTGGACACTT | 79876 |
rs761238888 | snp | A/G | 1.65302e-05 | 0.00287486 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132668908 | TTAAGTAAAGTTCAA[A/G]CAGCAGAACATACTC | 79876 |
rs761283391 | snp | C/T | | | intron-variant | ACAD11, UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132656917 | AGCATCATCAAGTTT[C/T]CGCCCATTTTTCTGG | 79876 |
rs761372183 | snp | C/T | 3.32662e-05 | 0.00407824 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132672189 | TAAAGTAAGTCAGGG[C/T]TAATTTTTCTGAATA | 79876 |
rs761407437 | snp | A/C | | | upstream-variant-2KB, intron-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132658536 | TAACTTGTCCAAATT[A/C]CACAGCAATTGAAAT | 79876 |
rs761619151 | snp | C/G | 1.65422e-05 | 0.0028759 | missense, intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675316 | AGGATTTTTTTCCTA[C/G]TATGTCCATGAAGCC | 79876 |
rs761758781 | snp | C/T | | | intron-variant, upstream-variant-2KB | ACAD11, UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132653061 | ACATGTACAGCAACA[C/T]TAGAAAGGGATCCAA | 79876 |
rs761795293 | snp | A/C | | | intron-variant, upstream-variant-2KB | ACAD11, UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132653920 | ATCTTCTTTTTGTCG[A/C]TGGCTCTCAAATTTA | 79876 |
rs761901685 | snp | A/G | | | downstream-variant-500B, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132678340 | AAGGCAGCTGATTAC[A/G]AAAAATTAATCATCA | 79876 |
rs761918115 | in-del | -/ATCCAT | 1.64991e-05 | 0.00287215 | upstream-variant-2KB, cds-indel, intron-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132659595 | GAGGCAAAGGCTGAC[-/ATCCAT]ACCTGTACTGGGCAA | 79876 |
rs761932331 | snp | A/T | 1.76052e-05 | 0.00296686 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132671736 | AATTACTTCTTGCTC[A/T]TTTATTTTTTTTCCT | 79876 |
rs761998975 | snp | C/T | 3.29788e-05 | 0.00406058 | synonymous-codon, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132671004 | ACCTGTTGATCTAGT[C/T]CTTAGCTGTGTGGAC | 79876 |
rs762024438 | snp | C/G | 1.64963e-05 | 0.00287192 | upstream-variant-2KB, utr-variant-5-prime, splice-donor-variant, intron-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132659602 | AGGCTGACATCCATA[C/G]CTGTACTGGGCAATG | 79876 |
rs762158063 | in-del | -/TC | 3.38387e-05 | 0.00411317 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132672012 | ACATCTCATACTTTT[-/TC]TCTTTTTTTTTGAAA | 79876 |
rs762177687 | snp | C/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132663257 | TTTCAGTTGAAAATC[C/T]GTTGAAGAAACAAAA | 79876 |
rs762382872 | snp | C/T | 1.78277e-05 | 0.00298555 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675800 | CCTTAAAAACTGACA[C/T]AGGATCAAATTTACA | 79876 |
rs762491043 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132659975 | CCCAATGTGTGTTCG[A/G]GTTTCAATTCTCCAG | 79876 |
rs762502767 | snp | C/G | 0.00019837 | 0.00995719 | synonymous-codon, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132666052 | GACTGCTGAAATGCT[C/G]ACAAGATGTGGCATT | 79876 |
rs762588346 | snp | C/T | 0.000148853 | 0.00862578 | synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132668848 | TATGACAAGGTGGAA[C/T]TAGCCAATATGAATA | 79876 |
rs762628468 | snp | A/G | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132669029 | TTCTCTATAAAATGC[A/G]GTTTTCACTTGTACA | 79876 |
rs762778183 | in-del | -/C | | | upstream-variant-2KB, intron-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132659415 | TTCCATTACCGCCCT[-/C]CAATTGGGAAGCCCC | 79876 |
rs762779162 | snp | C/T | 1.65814e-05 | 0.00287931 | stop-gained, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132672164 | GCTGGGATCTTAGTA[C/T]AAAACGTGTTAAAGT | 79876 |
rs762794075 | snp | A/G | 0.000210349 | 0.0102533 | upstream-variant-2KB, utr-variant-5-prime, missense, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132660577 | CAGCAGCGGGTCCAG[A/G]AGCTGGAGCGGGAAC | 79876 |
rs762890718 | in-del | -/TTTT | 7.59886e-05 | 0.00616348 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132672016 | CTCATACTTTTTCTC[-/TTTT]TTTTTGAAATGTGTT | 79876 |
rs762991189 | snp | A/G | | | intron-variant | ACAD11, UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132654908 | GGCTGATTTGAACCC[A/G]ATAGGACACACCTGA | 79876 |
rs763029530 | snp | A/G | 0.000138418 | 0.00831804 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132660721 | GCGTCGCCGGTCGGA[A/G]GCAGGCGCGGGGGAC | 79876 |
rs763048524 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132661963 | CTGACATCTCTAATC[A/G]GAATAAGTGGAAACT | 79876 |
rs763097263 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132659758 | TGGCTTCATGATCAC[C/T]CCCGCAGGCCACAGC | 79876 |
rs763145207 | snp | A/T | 1.65315e-05 | 0.00287498 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132676504 | GCTTGGAAGACCTCA[A/T]GGCCAAAATGAAGAA | 79876 |
rs763173306 | snp | A/G | 3.29864e-05 | 0.00406105 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132670982 | ATGGTGGGTTAGAAG[A/G]AGGAAAACCTGTTGA | 79876 |
rs763388472 | in-del | -/AG | | | intron-variant, nc-transcript-variant | NPHP3-ACAD11, UBA5 | GRCh38.p7 | 3:132678673 | TTATTTTTTTGAGAC[-/AG]AGTCTCACTCTGTTG | 79876 |
rs763418982 | snp | A/G | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132674005 | AATTTCTGAATTTAC[A/G]AAATATTTACTAAAT | 79876 |
rs763518648 | in-del | -/C | 1.70304e-05 | 0.00291803 | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132659756 | CTGGCTTCATGATCA[-/C]CCCCCGCAGGCCACA | 79876 |
rs763606373 | in-del | -/AT | 2.84006e-05 | 0.00376822 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675961 | CCATATGTAAATATC[-/AT]ATAAAATATTTATCA | 79876 |
rs763633418 | snp | C/G | 1.6516e-05 | 0.00287362 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132668851 | GACAAGGTGGAACTA[C/G]CCAATATGAATAGAC | 79876 |
rs763770764 | snp | C/T | 1.66252e-05 | 0.00288311 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132672045 | GTGTTTTATTTTTCA[C/T]GTAGTGTGCTCCACC | 79876 |
rs763776116 | snp | C/G | 6.89964e-05 | 0.00587311 | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132659776 | CGCAGGCCACAGCAA[C/G]GCGGCATCCACAGGT | 79876 |
rs763860645 | snp | C/T | 3.3184e-05 | 0.00407319 | synonymous-codon, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132672169 | GATCTTAGTACAAAA[C/T]GTGTTAAAGTAAGTC | 79876 |
rs763973062 | in-del | -/AATT | | | intron-variant, upstream-variant-2KB | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132661725 | CTCCCCAGTAAAAAC[-/AATT]AAGTCGTGTAGCTAA | 79876 |
rs764140265 | snp | G/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132667267 | AAGTGCTCTTGCATC[G/T]CTAACAAGCTTCAGG | 79876 |
rs764159106 | snp | A/G | 5.37764e-05 | 0.00518511 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132670311 | ATTTATGAATATTTT[A/G]TATAATGTCCAGCTC | 79876 |
rs764310247 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132678005 | TTGAATTTAAAAAAT[A/G]AAATGCAGTTTTTCA | 79876 |
rs764375500 | snp | A/G | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132676148 | ATTAATGAACCAAGT[A/G]TAGTAGATTTTGATT | 79876 |
rs764501665 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132658915 | GTTTATGTAACATAT[C/T]TAAACTCCCAGACAG | 79876 |
rs764562675 | snp | C/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132672399 | ATTAAATATTACATA[C/T]AATACATGTGTGCAT | 79876 |
rs764683347 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132661616 | AGTGAGAAAATTGAG[A/G]CTTAGAGAGCCACCT | 79876 |
rs764732753 | snp | A/T | 4.97088e-05 | 0.00498517 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675645 | AAGAGGTTATACAAG[A/T]AGAGGAAGAGATAAT | 79876 |
rs764818446 | snp | A/C | 1.65567e-05 | 0.00287716 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132665879 | ATGAGGTATGATAAA[A/C]CCTTTCCAAGTTTTT | 79876 |
rs764865650 | snp | A/C | | | intron-variant, upstream-variant-2KB | ACAD11, UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132654166 | GTCTCTTCCTTTCCT[A/C]GCCCACATTTAATCA | 79876 |
rs764929126 | snp | A/T | 1.64817e-05 | 0.00287064 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132671810 | CAAACATGGATGGAA[A/T]CTGGGGTCAGTGAAA | 79876 |
rs765075923 | snp | C/T | 1.65941e-05 | 0.00288041 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132666066 | TGACAAGATGTGGCA[C/T]TGGTAAGGTAAAAAC | 79876 |
rs765129157 | snp | C/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132667400 | CTGGTGTCCAGACTG[C/T]ACCCCATAATAAGTG | 79876 |
rs765201647 | snp | A/T | 0.000108184 | 0.00735393 | upstream-variant-2KB, utr-variant-5-prime, missense, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132660572 | GCCTGCAGCAGCGGG[A/T]CCAGGAGCTGGAGCG | 79876 |
rs765242964 | snp | C/G | 0.000167943 | 0.00916206 | upstream-variant-2KB, utr-variant-5-prime, missense, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132659745 | CGCCAGTAGCACCTG[C/G]CTTCATGATCACCCC | 79876 |
rs765309520 | in-del | -/AG | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675186 | ATTTTTAAAAAATTT[-/AG]GTGTTCTAGTATTTT | 79876 |
rs765318348 | snp | A/C/T | 0.000229581 | 0.0107117 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675948 | AAATATGATTTACCC[A/C/T]TATGTAAATATCATA | 79876 |
rs765373167 | in-del | -/GT | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132668163 | TGGCCATTTTAGTGT[-/GT]GTGTGTGTGTGTGTG | 79876 |
rs765381812 | snp | A/G | | | downstream-variant-500B, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132678382 | ATTACTAAACTCATA[A/G]CATTTGTCCAGATTT | 79876 |
rs765412110 | in-del | -/CAGCA | 1.65179e-05 | 0.00287379 | upstream-variant-2KB, utr-variant-5-prime, frameshift-variant, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132659707 | GAACTTGTGCTGGGG[-/CAGCA]CTTCGGCCAAATCGG | 79876 |
rs765475609 | snp | A/T | 5.01006e-05 | 0.00500478 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132668942 | GGTAAATGGAATAGC[A/T]ATCAAGTACCATATT | 79876 |
rs765492246 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132660357 | CTCCGAGGAAGGCCT[A/G]TGGGAGTCTCGGAGA | 79876 |
rs765529135 | snp | A/G/T | 3.30536e-05 | 0.00406521 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132676498 | GTGAAAGCTTGGAAG[A/G/T]CCTCATGGCCAAAAT | 79876 |
rs765565180 | snp | G/T | 5.67811e-05 | 0.00532797 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132670273 | CTTTCAACATTTCAT[G/T]GATAGAATAAGGTAA | 79876 |
rs765642345 | snp | A/G | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132672764 | AATCTGCTTTTAGAT[A/G]CCTCTGCTATCCAAA | 79876 |
rs765992202 | snp | A/G | 0.000241984 | 0.010997 | intron-variant, upstream-variant-2KB | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132661071 | TTGAGTTTCATTAAA[A/G]GCTTATCAATGCATC | 79876 |
rs766063059 | snp | C/T | 1.65625e-05 | 0.00287766 | synonymous-codon, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675620 | AAAAAGGTAGCAGCA[C/T]TGCCTAAACAAGAGG | 79876 |
rs766448523 | snp | C/T | 1.65743e-05 | 0.00287869 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132671760 | TTTTCCTTATGTTTT[C/T]ACCCATTTCTACTAA | 79876 |
rs766451375 | snp | A/G | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132667227 | CACAATCCCCAAATG[A/G]TTCATTTGCATATTA | 79876 |
rs766453456 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132662012 | ATTTTAAAATTTTAC[A/G]AATGAAGACTTTGAA | 79876 |
rs766539267 | in-del | -/AGA | 1.65334e-05 | 0.00287514 | cds-indel, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132672103 | AAAGACTCTGAAACG[-/AGA]AGGTGTTTGTGCAGC | 79876 |
rs766541591 | snp | C/G | 1.64893e-05 | 0.0028713 | upstream-variant-2KB, utr-variant-5-prime, missense, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132659643 | CCTCACGTTCGGCCC[C/G]AAAGCCAGACAAGTG | 79876 |
rs766635597 | snp | A/G | 1.65116e-05 | 0.00287324 | upstream-variant-2KB, utr-variant-5-prime, synonymous-codon, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132659704 | GTCGAACTTGTGCTG[A/G]GGCAGCACTTCGGCC | 79876 |
rs766644374 | snp | A/C | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132662328 | AGTACATTTTTGTCT[A/C]CAGTCCTCCTTGACA | 79876 |
rs766751608 | snp | A/C | 1.67413e-05 | 0.00289316 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132666079 | CATTGGTAAGGTAAA[A/C]ACATTTCTCTTTGCC | 79876 |
rs766848668 | snp | C/G | | | intron-variant, nc-transcript-variant | NPHP3-ACAD11, UBA5 | GRCh38.p7 | 3:132678678 | TTTTTGAGACAGAGT[C/G]TCACTCTGTTGCCCA | 79876 |
rs766932828 | in-del | -/GG | 8.30944e-05 | 0.00644518 | upstream-variant-2KB, utr-variant-5-prime, frameshift-variant, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132660665 | CCGCATCGAGAAGAT[-/GG]GAGCTCAGAGGTGGT | 79876 |
rs767024381 | snp | C/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132669383 | GCTATCTTCGCATCT[C/T]AGCCTCCTGAGTAGC | 79876 |
rs767107499 | snp | C/T | 4.96069e-05 | 0.00498006 | missense, intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675330 | ACTATGTCCATGAAG[C/T]CAAATCCTCAGTGTG | 79876 |
rs767139749 | snp | C/T | 3.32646e-05 | 0.00407814 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132672190 | AAAGTAAGTCAGGGC[C/T]AATTTTTCTGAATAG | 79876 |
rs767149224 | snp | C/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132671578 | AATATTTACTGACTG[C/T]GTCTTGAATACTGTC | 79876 |
rs767183858 | snp | A/G | 0.00017234 | 0.00928117 | upstream-variant-2KB, utr-variant-5-prime, missense, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132660643 | GGCGACGGAGGGGGC[A/G]GCCGGGTCCGCATCG | 79876 |
rs767273944 | snp | C/T | 0.000171482 | 0.00925807 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132660985 | TTAATTAGTCCGCCT[C/T]GCTGTGTATAAGACT | 79876 |
rs767470900 | snp | A/G | | | intron-variant | ACAD11, UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132654745 | CAGAATACTTGCTGT[A/G]TTTCCCTTCTCTATT | 79876 |
rs767509214 | snp | C/T | 1.65861e-05 | 0.00287972 | utr-variant-3-prime, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132676531 | AGAATATGTAGATAA[C/T]GGACTGGGATATATT | 79876 |
rs767687250 | snp | C/T | 1.64898e-05 | 0.00287135 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132671005 | CCTGTTGATCTAGTT[C/T]TTAGCTGTGTGGACA | 79876 |
rs767781183 | snp | C/T | 1.75705e-05 | 0.00296394 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132671737 | ATTACTTCTTGCTCT[C/T]TTATTTTTTTTCCTT | 79876 |
rs767850008 | snp | A/G | 0.000142003 | 0.00842503 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675802 | TTAAAAACTGACATA[A/G]GATCAAATTTACAGG | 79876 |
rs767916998 | snp | A/G | 1.66158e-05 | 0.0028823 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675665 | GAAGAGATAATCCAT[A/G]AAGATAATGAATGGG | 79876 |
rs767932738 | snp | C/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132674297 | TTATGTGATTTTCTC[C/T]GTATAGAAGCTTTTA | 79876 |
rs767939963 | snp | A/G | 4.95929e-05 | 0.00497936 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132666053 | ACTGCTGAAATGCTG[A/G]CAAGATGTGGCATTG | 79876 |
rs767954320 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132660151 | GGCCGTCAGACTGTC[C/G]AGCCTAAGAATAAAA | 79876 |
rs768027912 | snp | A/G | 1.65362e-05 | 0.00287538 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132676455 | TAGCAAGAAGATTCT[A/G]TCACTGAGTTAACAG | 79876 |
rs768058306 | snp | C/G | | | upstream-variant-2KB, intron-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132658853 | TCATTTCATTAATAA[C/G]ACTAATCAAAATAGG | 79876 |
rs768061607 | in-del | -/TTTA | 7.27581e-05 | 0.00603107 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675219 | CATGTTTTAAATTTC[-/TTTA]TTTAAGTCTATTTTG | 79876 |
rs768117654 | snp | C/T | 7.32986e-05 | 0.00605342 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132670235 | TTTGAAGTACACAAC[C/T]ATAATATAACCACAG | 79876 |
rs768338891 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132658476 | TCCTACAATATGAAC[A/G]TTACTATCTCCTTTT | 79876 |
rs768451738 | snp | A/G | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132670083 | GGTTGGGGTGCAGTG[A/G]GTGCGATGATAGCTC | 79876 |
rs768509328 | snp | C/T | 1.65611e-05 | 0.00287755 | missense, intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675298 | TTGGATACAATGCAA[C/T]GCAGGATTTTTTTCC | 79876 |
rs768599364 | snp | A/G | 1.67013e-05 | 0.0028897 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675574 | AACTGAGAATGAGTA[A/G]GAACACTTTGATGCT | 79876 |
rs768687133 | snp | C/T | 1.65921e-05 | 0.00288024 | utr-variant-5-prime, intron-variant, missense, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132665824 | TTCTTTGTTTTAAGC[C/T]GCTTGATGGCATTGA | 79876 |
rs768704548 | snp | C/T | | | intron-variant, upstream-variant-2KB | ACAD11, UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132653828 | CTTAATATTGGGGTG[C/T]CTTGGACTCAGTCTC | 79876 |
rs768865603 | snp | C/T | 4.56527e-05 | 0.00477748 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132670157 | AGCCTCTTGAAATGC[C/T]AGGATTACAGGCTTA | 79876 |
rs768878026 | snp | C/T | 1.68775e-05 | 0.0029049 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132671726 | ATTTATTGTAAATTA[C/T]TTCTTGCTCTTTTAT | 79876 |
rs769073598 | snp | A/C | 1.65021e-05 | 0.00287241 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132659590 | CGCTGGAGGCAAAGG[A/C]TGACATCCATACCTG | 79876 |
rs769080837 | snp | C/T | | | intron-variant | ACAD11, UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132655598 | CCCTTCAAGTCTTTG[C/T]TGAATGCCGTGTGCT | 79876 |
rs769218988 | snp | A/G | 1.64942e-05 | 0.00287173 | upstream-variant-2KB, utr-variant-5-prime, synonymous-codon, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132659679 | TTAGGTAGGCCTCCA[A/G]GGACTTGCTGTCGAA | 79876 |
rs769347927 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132677229 | ATTATATTCTGCACC[A/G]AACAAGGAACAGAAA | 79876 |
rs769409942 | snp | C/T | 1.86076e-05 | 0.00305016 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675779 | ATAATTATTGCTTAT[C/T]AAATTCCTTAAAAAC | 79876 |
rs769433883 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132659878 | CTGGCTCCAGCCAAC[A/C]GCACACAGCCTACGC | 79876 |
rs769500265 | snp | A/C | 1.68015e-05 | 0.00289836 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675884 | TCCAGTTCCAGACTT[A/C]CCTGAAGGAATTACA | 79876 |
rs769565577 | in-del | -/TG | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132670419 | TAGTACAGCAATTTT[-/TG]TGTAATTTTTATGTA | 79876 |
rs769590457 | snp | C/T | 1.68952e-05 | 0.00290642 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132668801 | TTTTCATCAGAATAC[C/T]ACTATTTTCATTTTA | 79876 |
rs769645376 | snp | A/G | 1.65573e-05 | 0.00287721 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132672146 | ACCACTATGGGTGTG[A/G]TTGCTGGGATCTTAG | 79876 |
rs769678266 | snp | C/T | 3.98859e-05 | 0.00446558 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132670183 | GCTTATAATCATTCC[C/T]TTTTTCCTTCTTAGG | 79876 |
rs769806924 | snp | C/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132674187 | AAGGTTGAACACTTA[C/T]ATTCTTCTGTGAATT | 79876 |
rs769837796 | in-del | -/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132672016 | CTCATACTTTTTCTC[-/T]TTTTTTTTGAAATGT | 79876 |
rs769890329 | snp | A/G | 6.63031e-05 | 0.00575736 | missense, intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675292 | TTTACCTTGGATACA[A/G]TGCAATGCAGGATTT | 79876 |
rs769894338 | snp | C/G/T | 1.65982e-05 | 0.00288077 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132671098 | GATTTATCTGTTTTC[C/G/T]TGTATATTCTATCAG | 79876 |
rs769919837 | snp | C/T | 6.65303e-05 | 0.00576721 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132665816 | ACATATTTTTCTTTG[C/T]TTTAAGCCGCTTGAT | 79876 |
rs769976328 | snp | A/G | 3.49339e-05 | 0.0041792 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132660719 | CTGCGTCGCCGGTCG[A/G]AGGCAGGCGCGGGGG | 79876 |
rs770055508 | snp | A/G | | | downstream-variant-500B, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132678469 | GCACAGAGACTCTAA[A/G]TGATAGTAAAACAAC | 79876 |
rs770143526 | snp | A/G | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132665060 | CATCTAACCAAGATG[A/G]CTATCTAACAATATT | 79876 |
rs770214645 | snp | A/G | 1.65026e-05 | 0.00287246 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132670967 | TTTCTTTGACTAGTA[A/G]TGGTGGGTTAGAAGA | 79876 |
rs770227806 | snp | A/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132663723 | TTAGTGTCCCACACT[A/T]AAATATGAACAGAAC | 79876 |
rs770381460 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132660269 | CCGGGTTTAGCCGGC[C/T]CAGCGAGGAAGGAAG | 79876 |
rs770390285 | snp | A/G | 1.65086e-05 | 0.00287298 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132659582 | TTTTTTTCCGCTGGA[A/G]GCAAAGGCTGACATC | 79876 |
rs770594099 | snp | A/T | | | intron-variant, upstream-variant-2KB | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132661430 | AAAAAATCAGTATGT[A/T]TAAAGGTCTTAGAGT | 79876 |
rs770647555 | snp | A/G | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132662927 | CATCAAGGTAAGGAT[A/G]GCAAATTCCTGTGAT | 79876 |
rs770666884 | snp | C/G | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132671339 | TTAGTATCTTATAAT[C/G]TTGGTCAGCATTAGT | 79876 |
rs770693243 | snp | G/T | 3.4195e-05 | 0.00413477 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132668785 | TAGTTTTTTGGTATG[G/T]TTTTCATCAGAATAC | 79876 |
rs770731051 | snp | C/T | 1.87549e-05 | 0.0030622 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675768 | ATACAAATTGAATAA[C/T]TATTGCTTATTAAAT | 79876 |
rs770749604 | snp | A/G | 0.00125981 | 0.0250662 | upstream-variant-2KB, utr-variant-5-prime, missense, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132660557 | CGGAGTCTGTGGAGC[A/G]CCTGCAGCAGCGGGT | 79876 |
rs770821132 | snp | A/G | 6.71321e-05 | 0.00579323 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675873 | AATTTTTCAGGTCCA[A/G]TTCCAGACTTACCTG | 79876 |
rs770861629 | snp | A/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132677348 | ACTCATTCTTTAGGC[A/T]ACTCCTGGATACTTC | 79876 |
rs770884092 | snp | A/G | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132673341 | TTTGAATACTAGATT[A/G]ATCACTCTTCTTTTT | 79876 |
rs770925003 | in-del | -/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132671736 | AATTACTTCTTGCTC[-/T]TTTATTTTTTTTCCT | 79876 |
rs771075583 | snp | C/T | 3.34504e-05 | 0.00408951 | synonymous-codon, intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675269 | GTTAAATTTTGGTAC[C/T]GTTAGTTTTTACCTT | 79876 |
rs771185612 | snp | C/G | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132665237 | AGGGAGAGGAAAATG[C/G]GGGTGGAGGCTGAAT | 79876 |
rs771295288 | snp | C/T | 1.99834e-05 | 0.0031609 | upstream-variant-2KB, utr-variant-5-prime, missense, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132660568 | GAGCGCCTGCAGCAG[C/T]GGGTCCAGGAGCTGG | 79876 |
rs771361395 | snp | A/G | 1.65209e-05 | 0.00287405 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132676483 | CAGTGGAAGATTCTG[A/G]TGAAAGCTTGGAAGA | 79876 |
rs771386440 | in-del | -/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132667799 | TTCCCAAGTTTAATG[-/T]TTCCCGCAACTTATG | 79876 |
rs771493106 | snp | A/T | 2.51007e-05 | 0.00354256 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132670255 | TATAACCACAGTGGA[A/T]AACTTTCAACATTTC | 79876 |
rs771541090 | snp | A/G | 3.30491e-05 | 0.00406491 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132670950 | ATGTTTTTCAAACTT[A/G]TTTTCTTTGACTAGT | 79876 |
rs771730809 | snp | A/G | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132664760 | CTTTGTAGTATAATG[A/G]TGAAGGAAGAGCCTA | 79876 |
rs771759605 | snp | C/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132673605 | TGCCCACCTCAGCCT[C/T]CCAAAGTGTTGGGAT | 79876 |
rs771764695 | snp | G/T | 1.65206e-05 | 0.00287403 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132659576 | TACAAATTTTTTTCC[G/T]CTGGAGGCAAAGGCT | 79876 |
rs771793223 | snp | C/T | | | intron-variant | ACAD11, UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132656643 | GGATTTACAGGTACC[C/T]ACCACCACACCCAGC | 79876 |
rs771807911 | snp | A/G | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132669662 | GAAGGCTGCACAAAA[A/G]CAGGTGGTGGGCCAG | 79876 |
rs771834658 | in-del | -/GTGTGT | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132668159 | CTAATGGCCATTTTA[-/GTGTGT]GTGTGTGTGTGTGTG | 79876 |
rs771877204 | snp | G/T | 1.66178e-05 | 0.00288247 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675597 | TTGATGCTGTTTGAT[G/T]TCTACAGAAAAAGGT | 79876 |
rs771902887 | in-del | -/ATT | 0.000132153 | 0.00812766 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132671888 | TGTTTTGCGGTATGC[-/ATT]ATTCTTTTTGGAATA | 79876 |
rs771918240 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132661066 | AAACTTTGAGTTTCA[C/T]TAAAGGCTTATCAAT | 79876 |
rs772013226 | snp | C/G | 1.65154e-05 | 0.00287358 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132665994 | CACAGAAAATCCGTA[C/G]CTTTGCCGTAGCAAT | 79876 |
rs772060943 | snp | C/G | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132674874 | AGCTTTCTTAATTAT[C/G]TCAGGGATTTAAAAA | 79876 |
rs772168913 | snp | C/G | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132667089 | ATGCTGATGTTGCTA[C/G]GATTACACCAGTAAG | 79876 |
rs772289840 | snp | A/T | 1.65081e-05 | 0.00287293 | upstream-variant-2KB, utr-variant-5-prime, missense, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132659699 | TTGCTGTCGAACTTG[A/T]GCTGGGGCAGCACTT | 79876 |
rs772377138 | snp | C/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132668474 | TGAAAGGGAATTAAT[C/T]TTAATTTCTGAGTAA | 79876 |
rs772443221 | snp | C/T | 1.69479e-05 | 0.00291095 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132672000 | ATACTATTTGGAACA[C/T]CTCATACTTTTTCTC | 79876 |
rs772448150 | snp | C/G | | | intron-variant, upstream-variant-2KB | ACAD11, UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132653663 | ACGTCCTCCTCCTAT[C/G]TTCTTAAACCCATTT | 79876 |
rs772532453 | snp | A/G | 1.6534e-05 | 0.00287519 | synonymous-codon, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132672091 | AAATATTGATGAAAA[A/G]ACTCTGAAACGAGAA | 79876 |
rs772542966 | snp | C/T | 0.000191173 | 0.00977496 | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132660531 | GTTGGCGGCCGGAGT[C/T]CCAGCCATGGCGGAG | 79876 |
rs772658862 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132659940 | CCCGAGGTTTTAGCT[C/T]TAGTCAAGTGCCAAA | 79876 |
rs772679697 | snp | A/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132677505 | GATCATGACCACTAA[A/T]CTGTAAATTGATATA | 79876 |
rs772799590 | snp | G/T | 1.65745e-05 | 0.00287871 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675612 | TTCTACAGAAAAAGG[G/T]AGCAGCACTGCCTAA | 79876 |
rs772888455 | snp | A/G | 1.65397e-05 | 0.00287569 | missense, intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675345 | CCAAATCCTCAGTGT[A/G]ATGACAGAAATTGCA | 79876 |
rs772889629 | snp | A/G | 1.65493e-05 | 0.00287652 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132665851 | TTGAAACGAATGGGA[A/G]TTGTAAGCGACTATG | 79876 |
rs773016010 | snp | A/G | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132674816 | TATACATTTAAGATT[A/G]TGCATTTTATAGTAA | 79876 |
rs773155430 | snp | C/T | 6.60447e-05 | 0.00574613 | synonymous-codon, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132666001 | AATCCGTACCTTTGC[C/T]GTAGCAATAGTAGGT | 79876 |
rs773209691 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132668905 | GGATTAAGTAAAGTT[C/G]AAGCAGCAGAACATA | 79876 |
rs773263197 | snp | A/C | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132671141 | ATCCTAAAAACAGTT[A/C]TGAATGTAAACCCTT | 79876 |
rs773352117 | in-del | -/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132672015 | CTCATACTTTTTCTC[-/T]TTTTTTTTTGAAATG | 79876 |
rs773384065 | snp | A/G | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132663811 | ATGTAAGATAAACAC[A/G]TCCCCCTAAATTATC | 79876 |
rs773387945 | snp | A/G | | | intron-variant | ACAD11, UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132654884 | AGCTGGTTGGAGTTA[A/G]CATAAATAGGCTGAT | 79876 |
rs773438827 | snp | A/T | 1.67086e-05 | 0.00289033 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132671744 | CTTGCTCTTTTATTT[A/T]TTTTCCTTATGTTTT | 79876 |
rs773526826 | snp | A/G | 1.69421e-05 | 0.00291046 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132672004 | TATTTGGAACATCTC[A/G]TACTTTTTCTCTTTT | 79876 |
rs773649942 | snp | A/G | 4.95119e-05 | 0.00497529 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132668887 | TTCCAACCTCATCAA[A/G]CAGGATTAAGTAAAG | 79876 |
rs773715700 | in-del | -/CAGAGTA | | | intron-variant, upstream-variant-2KB | ACAD11, UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132654417 | AAATCACTGACCACT[-/CAGAGTA]GTAAGCATATGTGTG | 79876 |
rs773826017 | snp | C/T | 3.30633e-05 | 0.00406578 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132676459 | AAGAAGATTCTGTCA[C/T]TGAGTTAACAGTGGA | 79876 |
rs773929339 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132661512 | AGTAGCAAGCAGTTA[C/T]TGAGCTTTCACTGTG | 79876 |
rs774051957 | snp | A/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132660799 | CTCATGGGGACGCCC[A/G]CCACCCTTTTCTTGG | 79876 |
rs774077344 | snp | A/G | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132673449 | ACCTCCTGAGCTCAA[A/G]TGATCCTCCCACCTC | 79876 |
rs774130118 | snp | C/T | | | intron-variant | ACAD11, UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132656424 | TGAGTTATTTTTCAA[C/T]AGCAGCTATACTAAT | 79876 |
rs774141219 | snp | A/T | 1.6549e-05 | 0.0028765 | missense, intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675304 | ACAATGCAATGCAGG[A/T]TTTTTTTCCTACTAT | 79876 |
rs774231165 | snp | G/T | 1.84147e-05 | 0.0030343 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132660745 | GGGGGACGAGGTCAG[G/T]CTCCGTGAGGTCAGA | 79876 |
rs774231185 | snp | C/T | 1.66818e-05 | 0.00288802 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675582 | ATGAGTAAGAACACT[C/T]TGATGCTGTTTGATT | 79876 |
rs774266355 | snp | C/T | | | intron-variant | ACAD11, UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132655162 | TATATACTTACACTA[C/T]GACCACTTCTTACCC | 79876 |
rs774318611 | snp | A/G | 1.65833e-05 | 0.00287948 | utr-variant-5-prime, intron-variant, missense, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132665825 | TCTTTGTTTTAAGCC[A/G]CTTGATGGCATTGAA | 79876 |
rs774340220 | snp | C/G | | | intron-variant | ACAD11, UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132657153 | TCTTTTATCTACCTG[C/G]AACTGTGTGAGATAA | 79876 |
rs774402385 | snp | A/C | 3.29848e-05 | 0.00406095 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132670989 | GTTAGAAGAAGGAAA[A/C]CCTGTTGATCTAGTT | 79876 |
rs774574069 | snp | C/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132665335 | TTAAACTGCAGATTA[C/T]CAGTAACTAGTTAAA | 79876 |
rs774583067 | snp | A/G | 1.65446e-05 | 0.00287612 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132671905 | TATTCTTTTTGGAAT[A/G]TTCTTCACTGTTAGA | 79876 |
rs774627226 | snp | A/G | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132666817 | TAAAAATATTTATTG[A/G]AATTTTAATACCTTT | 79876 |
rs774688820 | snp | G/T | 1.68491e-05 | 0.00290245 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132671730 | ATTGTAAATTACTTC[G/T]TGCTCTTTTATTTTT | 79876 |
rs774782762 | snp | A/T | 0.000131983 | 0.00812243 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132659595 | GAGGCAAAGGCTGAC[A/T]TCCATACCTGTACTG | 79876 |
rs775075107 | snp | A/C | 1.68007e-05 | 0.00289828 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675885 | CCAGTTCCAGACTTA[A/C]CTGAAGGAATTACAG | 79876 |
rs775081752 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132661458 | AGTAGCGCTTGTACA[C/T]GGCAAGCCTTATACA | 79876 |
rs775151731 | snp | C/T | 1.65269e-05 | 0.00287457 | synonymous-codon, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132666050 | GTGACTGCTGAAATG[C/T]TGACAAGATGTGGCA | 79876 |
rs775206325 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132658041 | TAATTTTTGTATCTT[C/T]AGTAGAGATGGGGGT | 79876 |
rs775225961 | snp | C/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132674898 | TTAAAAAATACACTT[C/T]TCCCACATTTTAGCT | 79876 |
rs775239838 | snp | A/G | 6.66856e-05 | 0.00577394 | synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132668820 | ATTTTCATTTTAGTT[A/G]CTACTCTTTGATTAT | 79876 |
rs775252380 | in-del | -/A | 1.66059e-05 | 0.00288144 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132671934 | GATACTTGAGTTCTT[-/A]GGGGCATTGAAAATG | 79876 |
rs775369367 | snp | C/T | 3.31565e-05 | 0.0040715 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132672162 | TTGCTGGGATCTTAG[C/T]ACAAAACGTGTTAAA | 79876 |
rs775378273 | snp | A/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132665235 | TGAGGGAGAGGAAAA[A/T]GGGGGTGGAGGCTGA | 79876 |
rs775417992 | in-del | -/AG | | | intron-variant | ACAD11, UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132657169 | AACTGTGTGAGATAA[-/AG]AGTCTAATTTCTATT | 79876 |
rs775434087 | snp | A/C | 1.7497e-05 | 0.00295774 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132660720 | TGCGTCGCCGGTCGG[A/C]GGCAGGCGCGGGGGA | 79876 |
rs775461439 | snp | C/G | 1.65682e-05 | 0.00287817 | missense, intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675295 | ACCTTGGATACAATG[C/G]AATGCAGGATTTTTT | 79876 |
rs775549663 | snp | A/G | 1.93785e-05 | 0.0031127 | upstream-variant-2KB, utr-variant-5-prime, missense, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132660575 | TGCAGCAGCGGGTCC[A/G]GGAGCTGGAGCGGGA | 79876 |
rs775703307 | snp | G/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132667113 | CAGTAAGAACCACTG[G/T]ATCCTTGCTCTACTC | 79876 |
rs775790523 | snp | A/G | | | intron-variant, upstream-variant-2KB | ACAD11, UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132653680 | TCTTAAACCCATTTC[A/G]ATCAAGCTTTCATTC | 79876 |
rs775814103 | snp | C/T | 1.65411e-05 | 0.00287581 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132671079 | TGTGCAAGATATATT[C/T]ATGGATTTATCTGTT | 79876 |
rs776043186 | snp | C/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675233 | CTTTATTTAAGTCTA[C/T]TTTGATTTTTCTAGG | 79876 |
rs776053118 | in-del | -/C | | | intron-variant, upstream-variant-2KB | ACAD11, UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132653749 | ACAAACCATGGTTTT[-/C]CCCCCACCTCTTTGG | 79876 |
rs776160212 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132660154 | CGTCAGACTGTCGAG[C/T]CTAAGAATAAAAAGA | 79876 |
rs776196650 | snp | A/G | 1.65081e-05 | 0.00287293 | synonymous-codon, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132666007 | TACCTTTGCCGTAGC[A/G]ATAGTAGGTGTTGGT | 79876 |
rs776295334 | snp | C/G | 1.656e-05 | 0.00287745 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675629 | GCAGCACTGCCTAAA[C/G]AAGAGGTTATACAAG | 79876 |
rs776372392 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132659861 | CGAGGCCGGGGTGGG[A/G]TCTGGCTCCAGCCAA | 79876 |
rs776386473 | snp | C/T | 1.86775e-05 | 0.00305588 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675775 | TTGAATAATTATTGC[C/T]TATTAAATTCCTTAA | 79876 |
rs776483647 | snp | A/T | 1.7029e-05 | 0.00291791 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132668791 | TTTGGTATGTTTTTC[A/T]TCAGAATACCACTAT | 79876 |
rs776579431 | snp | A/G | 1.65323e-05 | 0.00287505 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132672108 | CTCTGAAACGAGAAG[A/G]TGTTTGTGCAGCCAG | 79876 |
rs776585666 | in-del | -/GTGT | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132668161 | AATGGCCATTTTAGT[-/GTGT]GTGTGTGTGTGTGTG | 79876 |
rs776688921 | snp | A/G | 1.68108e-05 | 0.00289916 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132672026 | TTCTCTTTTTTTTTG[A/G]AATGTGTTTTATTTT | 79876 |
rs776731396 | snp | A/G | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132667306 | ATGCAGCTAGACCAC[A/G]CCATTTTGAGTAGCA | 79876 |
rs776948479 | snp | A/G | 0.000438212 | 0.0147957 | upstream-variant-2KB, utr-variant-5-prime, missense, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132660569 | AGCGCCTGCAGCAGC[A/G]GGTCCAGGAGCTGGA | 79876 |
rs776991393 | in-del | -/ATC | | | downstream-variant-500B, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132678349 | GATTACGAAAAATTA[-/ATC]ATCATTGAATTTAGT | 79876 |
rs776994336 | snp | G/T | 1.65214e-05 | 0.0028741 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132676489 | AAGATTCTGGTGAAA[G/T]CTTGGAAGACCTCAT | 79876 |
rs777084389 | snp | G/T | 2.59845e-05 | 0.00360438 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132670259 | ACCACAGTGGAAAAC[G/T]TTCAACATTTCATGG | 79876 |
rs777172295 | snp | C/T | 1.65233e-05 | 0.00287426 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132670951 | TGTTTTTCAAACTTA[C/T]TTTCTTTGACTAGTA | 79876 |
rs777202136 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132661623 | AAATTGAGGCTTAGA[G/T]AGCCACCTCAGGTTC | 79876 |
rs777215263 | snp | C/T | | | intron-variant, utr-variant-5-prime | ACAD11, UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132654581 | TCATGGCTGAGATGC[C/T]TGCAGAATCTCTGCC | 79876 |
rs777234104 | snp | C/G/T | 3.30285e-05 | 0.00406366 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132659578 | CAAATTTTTTTCCGC[C/G/T]GGAGGCAAAGGCTGA | 79876 |
rs777264408 | snp | C/T | 3.30453e-05 | 0.00406467 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132671057 | TAAATACAGTGAGTA[C/T]TCCTGCTGTGCAAGA | 79876 |
rs777343271 | in-del | -/GATG | 1.65526e-05 | 0.00287681 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132670934 | TGTATTTTGTGTCCT[-/GATG]TTTTTCAAACTTATT | 79876 |
rs777351354 | snp | A/G | 1.64814e-05 | 0.00287061 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132671843 | GCAGTTTCAGGGCAT[A/G]TACAGCTTATAATTC | 79876 |
rs777389328 | snp | A/G | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132662846 | TGATTAACCCAAACC[A/G]TTTCCCTCATCTGTA | 79876 |
rs777611847 | snp | A/T | 1.72e-05 | 0.00293253 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132668771 | TTTTTTGATATGTTT[A/T]GTTTTTTGGTATGTT | 79876 |
rs777768973 | snp | A/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132674543 | AAAAAAATACAAAAA[A/T]TAGCCAAGCGTGGTG | 79876 |
rs777808651 | snp | A/G | 3.14817e-05 | 0.00396735 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675965 | ATGTAAATATCATAT[A/G]AAATATTTATCATCT | 79876 |
rs777873836 | snp | C/G | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132673069 | AAGAAATTGAAAAAA[C/G]CATACATATAAACTC | 79876 |
rs777899489 | snp | A/T | 3.38101e-05 | 0.00411143 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132668966 | CCATATTCAGTGAAA[A/T]CTTACTTTATGTATT | 79876 |
rs778106383 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132657672 | ATTTTTGATGCTCCT[A/G]TAAGTTTTTGAAAAT | 79876 |
rs778163006 | snp | A/G | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132663613 | GAAAGACTGAAAGAC[A/G]CTGACATTGTGGGTT | 79876 |
rs778192026 | snp | A/C | 1.65343e-05 | 0.00287521 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132672098 | GATGAAAAGACTCTG[A/C]AACGAGAAGGTGTTT | 79876 |
rs778232284 | snp | C/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132664718 | ACAGGAAACAGTGGA[C/T]TAATACAGAATAAAG | 79876 |
rs778278215 | snp | C/T | 2.08779e-05 | 0.00323087 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675231 | TTCTTTATTTAAGTC[C/T]ATTTTGATTTTTCTA | 79876 |
rs778370826 | in-del | -/TGGG | 3.32027e-05 | 0.00407434 | utr-variant-3-prime, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132676535 | ATGTAGATAATGGAC[-/TGGG]TGGGATATATTGTAT | 79876 |
rs778379222 | snp | A/G | 1.65304e-05 | 0.00287488 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132670945 | TCCTGATGTTTTTCA[A/G]ACTTATTTTCTTTGA | 79876 |
rs778459928 | snp | C/G | 1.68207e-05 | 0.00290001 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132665787 | CTAATACCTAAAAGA[C/G]TGTAAGCTTTAAAAC | 79876 |
rs778516773 | snp | A/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132669268 | TTTTAATTTTTTTAA[A/T]TAAAAAATAAAATTT | 79876 |
rs778653244 | snp | A/G | 1.64885e-05 | 0.00287123 | upstream-variant-2KB, utr-variant-5-prime, synonymous-codon, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132659650 | TTCGGCCCCAAAGCC[A/G]GACAAGTGCTGGTTT | 79876 |
rs778668228 | snp | A/T | 1.65021e-05 | 0.00287241 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132671047 | CGAATGACAATAAAT[A/T]CAGTGAGTATTCCTG | 79876 |
rs778676844 | snp | G/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132664508 | TTTAAAAATAATTGA[G/T]GACAGTGTTTTAAAC | 79876 |
rs778781211 | in-del | -/T | 3.54566e-05 | 0.00421035 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132671741 | CTTCTTGCTCTTTTA[-/T]TTTTTTTCCTTATGT | 79876 |
rs778792369 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132676495 | CTGGTGAAAGCTTGG[A/G]AGACCTCATGGCCAA | 79876 |
rs778869265 | snp | A/G | 3.39807e-05 | 0.00412179 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675710 | ATAAATTGAAATGGC[A/G]GTATAAAACAAAACC | 79876 |
rs778898950 | snp | A/G | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132674726 | GGGAGCTGGAGGCAC[A/G]TGGGATGCTGAAAAT | 79876 |
rs778957097 | snp | C/T | 8.2603e-05 | 0.00642609 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132665990 | ATTTCACAGAAAATC[C/T]GTACCTTTGCCGTAG | 79876 |
rs779014409 | snp | A/G | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132663969 | GGAAAATAAAGTTGA[A/G]AGAAATCATCCAGAG | 79876 |
rs779047931 | snp | A/G/T | 6.72296e-05 | 0.00579749 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675853 | TTTCAGAAGAGGAAC[A/G/T]GAAAAATTTTTCAGG | 79876 |
rs779051289 | snp | C/T | 1.70348e-05 | 0.00291841 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132666100 | TCTCTTTGCCTGTCA[C/T]ATAGGGAACTACTCA | 79876 |
rs779305265 | snp | C/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132668337 | AGTCAGGTTATACTA[C/T]ATTTTAAGTTACAGC | 79876 |
rs779326368 | snp | A/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675214 | TTTTTCATGTTTTAA[A/T]TTTCTTTATTTAAGT | 79876 |
rs779358320 | snp | A/C | | | intron-variant, upstream-variant-2KB | ACAD11, UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132653587 | CTTTCTCTTGACCTC[A/C]CTTCCCCCCTACTTA | 79876 |
rs779391652 | snp | A/G | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132664946 | GAAAATACATAGGAA[A/G]TTAAGCATCAGGAGA | 79876 |
rs779415068 | snp | A/G | 8.37837e-05 | 0.00647185 | upstream-variant-2KB, utr-variant-5-prime, missense, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132660653 | GGGGCGGCCGGGTCC[A/G]CATCGAGAAGATGAG | 79876 |
rs779426395 | snp | C/T | 1.6537e-05 | 0.00287545 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132672081 | TAGTTGCTGCAAATA[C/T]TGATGAAAAGACTCT | 79876 |
rs779530886 | snp | A/T | 3.32662e-05 | 0.00407824 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132676431 | CACTGTATTTCCCTT[A/T]TTTGTCAATAGCAAG | 79876 |
rs779557250 | snp | C/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132673353 | ATTGATCACTCTTCT[C/T]TTTGTTTTTTTGGAG | 79876 |
rs779566025 | snp | C/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132669784 | AGTTGTAGGTAGTTA[C/T]TGGACATGGTTAAGT | 79876 |
rs779804715 | snp | A/C/G | 0.000184491 | 0.00960295 | utr-variant-3-prime, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132676566 | TTCTCATGTTAAAGC[A/C/G]TCTTCCCTTGAAATT | 79876 |
rs779873223 | snp | C/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132676813 | TTGGCCTTTTGGAGT[C/G]GGGGAAGGACAAATC | 79876 |
rs779906517 | snp | A/G | | | intron-variant, upstream-variant-2KB | ACAD11, UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132652551 | GCAAAACTCCCATCC[A/G]TGTTAAATCCATTTT | 79876 |
rs779936725 | snp | A/G | 1.64966e-05 | 0.00287194 | upstream-variant-2KB, utr-variant-5-prime, synonymous-codon, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132659605 | CTGACATCCATACCT[A/G]TACTGGGCAATGGTC | 79876 |
rs779990586 | snp | G/T | 1.65611e-05 | 0.00287755 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132670929 | TAGAGTGTATTTTGT[G/T]TCCTGATGTTTTTCA | 79876 |
rs780061591 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132660493 | GTGGGGCGAAGGCGG[C/T]GGCGAAGGCCCGGGC | 79876 |
rs780110027 | snp | A/C | 6.65126e-05 | 0.00576644 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675433 | ATATTGAATAGGACA[A/C]TACATAAACAGATTT | 79876 |
rs780197321 | snp | G/T | 6.67925e-05 | 0.00577856 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675680 | GAAGATAATGAATGG[G/T]GTAGGTATTCTTTTA | 79876 |
rs780215968 | snp | A/C | | | upstream-variant-2KB, intron-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132659009 | GTTATTTTTAGAATA[A/C]AGTTTTAAGAATGTA | 79876 |
rs780273845 | snp | A/T | 3.32231e-05 | 0.00407559 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132665820 | ATTTTTCTTTGTTTT[A/T]AGCCGCTTGATGGCA | 79876 |
rs780296092 | snp | C/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132672420 | ATGTGTGCATATTCA[C/T]ACGTGAATATATGTG | 79876 |
rs780307709 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132677450 | TTCTAAACTGCCTCT[A/G]CAATGACTTGTAGTC | 79876 |
rs780425506 | snp | G/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132670071 | CTCTGTCCCCCAGGT[G/T]GGGGTGCAGTGGGTG | 79876 |
rs780429694 | snp | C/G | | | intron-variant | ACAD11, UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132655474 | AGGCATTTGGGCTGT[C/G]TTTCCTCAACACACT | 79876 |
rs780658128 | snp | C/T | 1.64955e-05 | 0.00287184 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132671871 | TTCCTGGAGAATCTG[C/T]TTGTTTTGCGGTATG | 79876 |
rs780673385 | snp | C/T | 6.59652e-05 | 0.00574267 | upstream-variant-2KB, utr-variant-5-prime, missense, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132659673 | GCTGGTTTAGGTAGG[C/T]CTCCAGGGACTTGCT | 79876 |
rs780709187 | snp | A/G | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132668038 | CCCATTTTTGTTTTT[A/G]TTGTTTAGTGTGCTG | 79876 |
rs780764978 | snp | C/T | 0.000268853 | 0.0115911 | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132660504 | GCGGCGGCGAAGGCC[C/T]GGGCTGGGAGCGTTG | 79876 |
rs780883035 | snp | A/C | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132676882 | TCTGTTGCATGAGGA[A/C]ATGGACAATAAAGTA | 79876 |
rs780983764 | snp | A/G | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132673899 | TGAACTCCTGGGCTC[A/G]AGCAGTCTGCCCATA | 79876 |
rs781045424 | snp | A/T | 1.67891e-05 | 0.00289729 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675882 | GGTCCAGTTCCAGAC[A/T]TACCTGAAGGAATTA | 79876 |
rs781106553 | snp | A/C | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132662563 | CAAAAGGTTATAGGA[A/C]AGGGATATGTATGTG | 79876 |
rs781220018 | snp | A/G | 4.41803e-05 | 0.00469981 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132670167 | AATGCTAGGATTACA[A/G]GCTTATAATCATTCC | 79876 |
rs781312726 | snp | C/T | 1.65756e-05 | 0.00287881 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675392 | ATATAAGGTATATGA[C/T]AATCTGTTAGAATGC | 79876 |
rs781315472 | snp | A/T | 1.65734e-05 | 0.00287862 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132670919 | TATAATGTATTAGAG[A/T]GTATTTTGTGTCCTG | 79876 |
rs781419204 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132657574 | TGGCATCTCTCAATT[C/T]TTAAAATTCTTTTTA | 79876 |
rs781430635 | snp | A/T | 1.66885e-05 | 0.00288859 | missense, intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132675273 | AATTTTGGTACTGTT[A/T]GTTTTTACCTTGGAT | 79876 |
rs781453211 | in-del | -/C | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132665778 | TTTGTATTACTAATA[-/C]CTAAAAGACTGTAAG | 79876 |
rs781481137 | snp | A/C | 3.2987e-05 | 0.00406108 | missense, intron-variant, nc-transcript-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132670980 | TAATGGTGGGTTAGA[A/C]GAAGGAAAACCTGTT | 79876 |
rs781536231 | snp | A/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132672877 | AGTTTATGAATCAAC[A/T]CATACTTTATTAAAA | 79876 |
rs781575444 | snp | C/T | | | intron-variant | ACAD11, UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132655637 | TCTTCCTGCCCCACA[C/T]CCAAACATTTCCTAT | 79876 |
rs781605897 | snp | C/G | 0.000123221 | 0.00784827 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | UBA5, ACAD11, NPHP3-ACAD11 | GRCh38.p7 | 3:132660713 | GGTAACCTGCGTCGC[C/G]GGTCGGAGGCAGGCG | 79876 |
rs781676124 | in-del | -/A | 1.70931e-05 | 0.0029234 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132666106 | GCCTGTCATATAGGG[-/A]AACTACTCACTCCTG | 79876 |
rs781682144 | snp | A/G | 1.67253e-05 | 0.00289178 | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132665803 | TGTAAGCTTTAAAAC[A/G]TATTTTTCTTTGTTT | 79876 |
rs796256562 | in-del | -/CTC | | | intron-variant, upstream-variant-2KB | ACAD11, UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132653635 | TTCGTAGAAAAACTC[-/CTC]AAGAGATTACACGTC | 79876 |
rs796575512 | snp | C/T | | | intron-variant | UBA5, NPHP3-ACAD11 | GRCh38.p7 | 3:132676207 | TAGTTTTAGCTACGA[C/T]GTCGTTTAAAAAGCT | 79876 |