SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6325244 | snp | A/C | 0.5 | 0 | intron-variant | Ubxn11 | Mm_Celera | 4:134113647 | AGAACCCTGAGCACA[A/C]GAGCACTCTTCCTTA | 67586 |
rs13461695 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime | Sh3bgrl3, Ubxn11 | GRCm38.p3 | 4:134127560 | TAAGCCCTGACGATG[A/G]CTGTCCCCAGCCACA | 67586 |
rs13468675 | snp | A/G | | | missense, nc-transcript-variant | Ubxn11 | Mm_Celera | 4:134126609 | ATTCAGCTGCCTTTG[A/G]GATCTTGAGCACCTT | 67586 |
rs27544023 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime, downstream-variant-500B | Sh3bgrl3, Ubxn11 | Mm_Celera | 4:134127663 | GGTCTGGGTCTGGGT[C/T]TGCAGATTAGGACGA | 67586 |
rs27544024 | snp | C/T | 0.124444 | 0.216185 | downstream-variant-500B, intron-variant, utr-variant-3-prime | Ubxn11, Sh3bgrl3 | Mm_Celera | 4:134126912 | TGGGTTCCTGTTCTC[C/T]AAGTTGTACTAAGTG | 67586 |
rs27544025 | snp | C/T | 0.401235 | 0.199068 | downstream-variant-500B, utr-variant-3-prime | Ubxn11 | Mm_Celera | 4:134126784 | CCCCTGACATAAGCT[C/T]CACAAGGCTCTCCAG | 67586 |
rs27544026 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ubxn11 | Mm_Celera | 4:134126343 | AGGGAGCTGGGGAGC[A/G]CTGAAGGCCTCTGGA | 67586 |
rs27544027 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Ubxn11 | Mm_Celera | 4:134126176 | TTAGGTGAGACCTAG[A/G]CTCCAGCCACTCTCC | 67586 |
rs27544028 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Ubxn11 | Mm_Celera | 4:134125942 | TCCCTTTCAGATGAC[C/T]GCAGGCTAGGTTAGG | 67586 |
rs27544029 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubxn11 | Mm_Celera | 4:134125590 | CCCTTGAGGTCCTCC[C/T]TGCAGCGCACTGCCC | 67586 |
rs27544030 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubxn11 | Mm_Celera | 4:134125416 | AGCTTGGCCCAGGTG[C/T]GCCTGGCTAATGTCC | 67586 |
rs27544031 | snp | A/G | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Ubxn11 | Mm_Celera | 4:134124271 | AGCTTCTGAAGCCAC[A/G]TGGTTCGGGTAGAAG | 67586 |
rs27544032 | snp | C/T | 0.456747 | 0.140554 | intron-variant, downstream-variant-500B | Ubxn11 | GRCm38.p3 | 4:134124197 | CCAGCATTCAGGGCA[C/T]CTTAACAGCGCAACT | 67586 |
rs27544033 | snp | A/T | 0.231111 | 0.249285 | intron-variant, downstream-variant-500B | Ubxn11 | Mm_Celera | 4:134124145 | GCATCTTGAAGGTAC[A/T]ACATTGCCAATGGGA | 67586 |
rs27544034 | snp | A/G | 0.124444 | 0.216185 | intron-variant, utr-variant-3-prime | Ubxn11 | Mm_Celera | 4:134123808 | GGCATGACATAGATG[A/G]CTGCAGAGGCCTCAC | 67586 |
rs27544035 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Ubxn11 | GRCm38.p3 | 4:134123627 | GAGCTCTGGGTCCAT[A/G]CCTACTCACACTCAC | 67586 |
rs27544036 | snp | A/G | 0.231111 | 0.249285 | missense, nc-transcript-variant | Ubxn11 | Mm_Celera | 4:134123428 | AGGTGGACTTTGACA[A/G]ACTGATGGCCAGTCT | 67586 |
rs27544037 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubxn11 | Mm_Celera | 4:134123288 | ATCCAATAGCTGCCA[C/T]TGTTAGCTAGTGTGG | 67586 |
rs27544038 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Ubxn11 | Mm_Celera | 4:134122716 | CCAAGTTAGCCCTCA[C/T]GCAGCCACTTCCTTG | 67586 |
rs27544039 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Ubxn11 | Mm_Celera | 4:134122388 | ACTGTGCAGGGCCAC[A/G]TGTGCAGCAGTTTCC | 67586 |
rs27544040 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Ubxn11 | Mm_Celera | 4:134122337 | CTTTTATGGCACCTT[C/T]CTGAGTGTCCTGGTT | 67586 |
rs27544041 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Ubxn11 | GRCm38.p3 | 4:134122027 | CCAGTCAACCCTGCT[C/T]CCTCCGGTTGGCCCC | 67586 |
rs27544042 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ubxn11 | Mm_Celera | 4:134121859 | CATCCTGCCACAAAA[C/T]AGCTCTCAGCAAGCT | 67586 |
rs27544043 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ubxn11 | Mm_Celera | 4:134121641 | CAGGAGGTGCAATAC[A/G]GCGGACTGTTGGTGG | 67586 |
rs27544044 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Ubxn11 | Mm_Celera | 4:134121274 | CTAGATGTCCTTTTC[A/G]AGGCAGAAAGCAGAC | 67586 |
rs27544045 | snp | A/T | 0.387812 | 0.208586 | intron-variant | Ubxn11 | Mm_Celera | 4:134121005 | TCTTGGCCTATACTG[A/T]CTTGTGTGGAAGCTC | 67586 |
rs27544046 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ubxn11 | Mm_Celera | 4:134120746 | CAGGTCCACTGACAT[A/G]ATCTTGAGGCCAGGT | 67586 |
rs27544047 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Ubxn11 | Mm_Celera | 4:134120745 | TCAGGTCCACTGACA[G/T]GATCTTGAGGCCAGG | 67586 |
rs27544048 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Ubxn11 | Mm_Celera | 4:134120703 | CCTGGAGCATGGTAC[C/T]TCACAAGGCCTCCAA | 67586 |
rs27544049 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ubxn11 | Mm_Celera | 4:134120696 | CACATGACCTGGAGC[A/C]TGGTACCTCACAAGG | 67586 |
rs27544050 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ubxn11 | GRCm38.p3 | 4:134120664 | AGCTGAGTGAGTCAC[A/G]TAGGTCCTGTAGGGC | 67586 |
rs27544051 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ubxn11 | GRCm38.p3 | 4:134120197 | ATCATACCCAAAATG[A/G]CGAGAATGTGTGACC | 67586 |
rs27544052 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Ubxn11 | Mm_Celera | 4:134120042 | GACTTTCTGAGCCTA[A/G]CAGAACCACACTGCT | 67586 |
rs27544053 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Ubxn11 | Mm_Celera | 4:134119946 | CACACAGGGCCTCTG[G/T]GTATCTACCATTGCT | 67586 |
rs27544054 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Ubxn11 | Mm_Celera | 4:134119819 | GCTGTTTTCTGATGC[A/G]AGAGGCTGAGAGGTG | 67586 |
rs27544055 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ubxn11 | Mm_Celera | 4:134119724 | TGAGGGTGTGCTCGG[A/G]AACTACCCAGAGGCT | 67586 |
rs27544056 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Ubxn11 | Mm_Celera | 4:134119575 | TGACACCCAGGAGCA[G/T]GCAGTACAGTGCTTG | 67586 |
rs27544057 | snp | A/T | 0.375 | 0.216506 | intron-variant | Ubxn11 | GRCm38.p3 | 4:134119445 | CTGGGGCTGCTGCCG[A/T]AGCTGTGCCAGTGTC | 67586 |
rs27544058 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Ubxn11 | Mm_Celera | 4:134119148 | CAGAGCAGGTTTTGG[A/G]CCTGGGTGAAGAGAA | 67586 |
rs27544059 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ubxn11 | Mm_Celera | 4:134118980 | AATGGACTAGATCCA[A/G]AACTTTTGCCTTAGG | 67586 |
rs27544060 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Ubxn11 | Mm_Celera | 4:134118896 | TGTGTCTGGGCATCC[A/G]TCCGTCACTTCCTAC | 67586 |
rs27544061 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ubxn11 | Mm_Celera | 4:134118895 | TTGTGTCTGGGCATC[C/T]GTCCGTCACTTCCTA | 67586 |
rs27544062 | snp | C/G | 0.32 | 0.24 | intron-variant | Ubxn11 | Mm_Celera | 4:134118805 | GAGCTTTTCCTCCTC[C/G]GAGCTCCCTCTTGTC | 67586 |
rs27544063 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ubxn11 | GRCm38.p3 | 4:134118731 | CTTGCTTTTGCCTTC[C/T]GGTGTGGGACAGACC | 67586 |
rs27544064 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ubxn11 | Mm_Celera | 4:134118682 | CGAGCCTTCCACGTC[A/G]GGGTTCCTGGGCCAC | 67586 |
rs27544065 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ubxn11 | Mm_Celera | 4:134118641 | GGCCGCTCCAGGCCT[A/G]GCTCTGAAGCCGTGG | 67586 |
rs27544066 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Ubxn11 | Mm_Celera | 4:134118542 | GACCACATGGCTGAT[A/C]TCTGAACGCATCTTC | 67586 |
rs27544067 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Ubxn11 | Mm_Celera | 4:134118121 | AGAAGATGAGGTAGG[C/T]GCTGCTGTGGAGGAC | 67586 |
rs27559968 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Ubxn11 | GRCm38.p3 | 4:134118053 | AGAGTAGCTGATGAC[A/G]GCTGAACAGAGGGCG | 67586 |
rs27559969 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Ubxn11 | GRCm38.p3 | 4:134117789 | ACTTGGGCCTGGGCT[C/T]CATCTCTCTGCCCCT | 67586 |
rs27559970 | snp | C/G | 0.492188 | 0.0620098 | intron-variant | Ubxn11 | GRCm38.p3 | 4:134117223 | TTCGGGAACAGGAAT[C/G]GTGGCAGCACCGCCC | 67586 |
rs27559971 | snp | C/G/T | 0.396694 | 0.202437 | intron-variant | Ubxn11 | GRCm38.p3 | 4:134117201 | CTGGTTTCTGCTTCC[C/G/T]GGGCTTTTCGGGAAC | 67586 |
rs27559972 | snp | C/T | 0.5 | 0 | intron-variant | Ubxn11 | GRCm38.p3 | 4:134117042 | ATCCATCTGTAGGAA[C/T]TCAGACCCCCTCATT | 67586 |
rs27559973 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Ubxn11 | GRCm38.p3 | 4:134116946 | ATCACTGTTAACCAT[A/G]GGTATTTAGTGGGGA | 67586 |
rs27559974 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Ubxn11 | GRCm38.p3 | 4:134116792 | TTCTCATGGTTTGTC[C/G]TCATCCTTCATTTTG | 67586 |
rs27559975 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ubxn11 | Mm_Celera | 4:134116320 | TCCCTGGCCTTACTT[C/T]AGTCTCTGCTTGCTC | 67586 |
rs27559976 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Ubxn11 | GRCm38.p3 | 4:134116273 | GTTGTGAGTTACCTA[C/T]GTCATCAGGGAAAGA | 67586 |
rs27559977 | snp | C/G | 0.487535 | 0.077957 | intron-variant | Ubxn11 | GRCm38.p3 | 4:134116223 | AGAGGCCCATTGTTT[C/G]AAGCCCTGCCATCCC | 67586 |
rs27559978 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Ubxn11 | GRCm38.p3 | 4:134116220 | TCCAGAGGCCCATTG[C/T]TTGAAGCCCTGCCAT | 67586 |
rs27559979 | snp | A/G | 0.231111 | 0.249285 | missense, nc-transcript-variant, intron-variant, utr-variant-5-prime | Ubxn11 | Mm_Celera | 4:134116040 | CCATAGCGGTTTCTC[A/G]GCGACTATGGCCTGC | 67586 |
rs27559980 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Ubxn11 | Mm_Celera | 4:134115749 | ACCCACAAAGTCCTC[A/G]GAGTTCTAGAGTAAT | 67586 |
rs27559981 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Ubxn11 | GRCm38.p3 | 4:134115748 | GACCCACAAAGTCCT[C/T]GGAGTTCTAGAGTAA | 67586 |
rs27559982 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Ubxn11 | Mm_Celera | 4:134115621 | ATGCGCACCTGCACA[C/T]ACCTGGGATCGCAGC | 67586 |
rs27559983 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ubxn11 | Mm_Celera | 4:134114938 | AAGAGCCATAACAGG[A/G]AGAGCGTGGTTGGAG | 67586 |
rs27559984 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ubxn11 | Mm_Celera | 4:134114540 | TGTGTGCCATTACCG[C/T]GTGTCTGATTCATCA | 67586 |
rs27559985 | snp | C/G | 0.188366 | 0.242283 | intron-variant | Ubxn11 | Mm_Celera | 4:134114373 | AGCAAGGACCTTTCA[C/G]GTGTTTATTGAGTCC | 67586 |
rs27559986 | snp | G/T | 0.18 | 0.24 | intron-variant | Ubxn11 | Mm_Celera | 4:134113770 | TCCAGCCACGCCACA[G/T]CATCTTCCTCTGGTT | 67586 |
rs27559987 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Ubxn11 | GRCm38.p3 | 4:134113764 | CTACGCTCCAGCCAC[A/G]CCACATCATCTTCCT | 67586 |
rs27559988 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ubxn11 | GRCm38.p3 | 4:134113762 | CTCTACGCTCCAGCC[A/G]CGCCACATCATCTTC | 67586 |
rs27559989 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ubxn11 | GRCm38.p3 | 4:134113752 | TCTGGAACCTCTCTA[C/T]GCTCCAGCCACGCCA | 67586 |
rs27559990 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Ubxn11 | Mm_Celera | 4:134113650 | ACCCTGAGCACACGA[C/G]CACTCTTCCTTAATA | 67586 |
rs27559991 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ubxn11 | Mm_Celera | 4:134113443 | ATGGAGGTAAGACTG[A/G]TGGAATGGACAGCCA | 67586 |
rs27559992 | snp | A/C | 0.46875 | 0.121031 | intron-variant, utr-variant-5-prime | Ubxn11 | GRCm38.p3 | 4:134111378 | TACAGGCTCCTCAAG[A/C]GTTCCAAATAGCTCT | 67586 |
rs27559993 | snp | A/G | 0.489796 | 0.070696 | intron-variant, utr-variant-5-prime | Ubxn11 | GRCm38.p3 | 4:134111092 | GGCACATCTCTATCC[A/G]AGGCACTCAAGCTCT | 67586 |
rs27559994 | snp | C/G | 0.56 | 0.195959 | intron-variant, utr-variant-5-prime | Ubxn11 | GRCm38.p3 | 4:134110701 | TCCAGGCTGCCACCA[C/G]GCCACACACTGGCAG | 67586 |
rs27559995 | snp | C/T | 0.46875 | 0.121031 | intron-variant, utr-variant-5-prime | Ubxn11 | Mm_Celera | 4:134110657 | GTCCTCAGTACCTCC[C/T]TTTCTTCGCCAGTAT | 67586 |
rs27559996 | snp | C/T | 0.5 | 0 | intron-variant, utr-variant-5-prime | Ubxn11 | Mm_Celera | 4:134109825 | CCTAAAGCCACAGGT[C/T]AGGAATCTGGCCAAG | 67586 |
rs27559997 | snp | A/G | 0.493827 | 0.0552116 | intron-variant, upstream-variant-2KB | Ubxn11 | GRCm38.p3 | 4:134109376 | CAGAGCTATGGGAAG[A/G]CCAGAGATGTGGACC | 67586 |
rs27559998 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Ubxn11 | Mm_Celera | 4:134107546 | TTTGGCTCTAGGCTT[A/G]TTAGATTTTAGTCCT | 67586 |
rs27559999 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Ubxn11 | Mm_Celera | 4:134106913 | TGCTTGTAAGCATCC[A/G]TGAAGGGAGCCACTA | 67586 |
rs27560000 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Ubxn11 | Mm_Celera | 4:134102732 | CCGAGGGTCGGCGAC[A/G]TGCATGACTTGGCTC | 67586 |
rs27560001 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | Ubxn11 | GRCm38.p3 | 4:134102549 | GGTTCGTTAGAGAGC[C/T]TCTCGGAATTAGCCA | 67586 |
rs27560002 | snp | C/G | 0.277778 | 0.248452 | upstream-variant-2KB | Ubxn11 | GRCm38.p3 | 4:134101945 | TCTAGTACTTTGGTG[C/G]TATTAGGATAATTTT | 67586 |
rs27560003 | snp | A/T | 0.124444 | 0.216185 | upstream-variant-2KB | Ubxn11 | Mm_Celera | 4:134101895 | TTACCCTGTCTGTAC[A/T]GGTGAGGACCCAGTG | 67586 |
rs27560004 | snp | A/G | 0.142012 | 0.225474 | upstream-variant-2KB | Ubxn11 | Mm_Celera | 4:134100837 | AGAAAGTTTTCCAGG[A/G]TCTCTAAGATGGTAC | 67586 |
rs27560005 | snp | A/T | 0.444444 | 0.157135 | upstream-variant-2KB | Ubxn11 | GRCm38.p3 | 4:134100828 | GGAGACCCCAGAAAG[A/T]TTTCCAGGGTCTCTA | 67586 |
rs27560006 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB | Ubxn11 | Mm_Celera | 4:134100661 | AGCTAAAAGTCAAGT[A/G]GATTCTGTCCACCCA | 67586 |
rs27560007 | snp | C/T | 0.165289 | 0.235211 | upstream-variant-2KB | Ubxn11 | Mm_Celera | 4:134100601 | CTCTCAATAAACTCC[C/T]TAGCCCCAAAGGAGC | 67586 |
rs31755922 | snp | A/G | 0.32 | 0.24 | intron-variant | Ubxn11 | GRCm38.p3 | 4:134106990 | CCACAGAGCAATGCC[A/G]GGATGGGGAGGATGC | 67586 |
rs31780922 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ubxn11 | Mm_Celera | 4:134105278 | GCATGGGCCCATCTA[C/T]ACAAATGAATAAACA | 67586 |
rs31788408 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Ubxn11 | GRCm38.p3 | 4:134109173 | ACCAGCCTACATCTT[C/T]TTACAGCTAGGCATG | 67586 |
rs31820623 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ubxn11 | GRCm38.p3 | 4:134116666 | TGTCTGGTTGGGGAG[A/G]TGGGAAAGGAGGGAA | 67586 |
rs31835879 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ubxn11 | GRCm38.p3 | 4:134106789 | CTCCCCAGGTCCTGG[A/G]ATTAAAGTGTGCACC | 67586 |
rs31841978 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ubxn11 | GRCm38.p3 | 4:134112882 | CACTCACACCTGGTC[C/T]CCACCTACTCACCCT | 67586 |
rs31953581 | snp | C/T | 0.375 | 0.216506 | downstream-variant-500B, intron-variant, utr-variant-3-prime | Ubxn11, Sh3bgrl3 | Mm_Celera | 4:134126951 | GGAGGGAGTGGCCAG[C/T]CCTAGCTGGGCTGAC | 67586 |
rs31958737 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ubxn11 | GRCm38.p3 | 4:134106564 | CAGGGAGAGTCAGGT[A/G]GGTAGGGATAAGTTG | 67586 |
rs31959374 | snp | A/G | 0.32 | 0.24 | intron-variant, utr-variant-5-prime | Ubxn11 | GRCm38.p3 | 4:134111552 | GAACTCACTATGTAG[A/G]CTAGGCTAGCTCCCA | 67586 |
rs31967694 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ubxn11 | Mm_Celera | 4:134112889 | ACCTGGTCCCCACCT[A/T]CTCACCCTGAGTCTC | 67586 |
rs31974640 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ubxn11 | GRCm38.p3 | 4:134116764 | GGGTGGGATCTGCCC[C/T]GGCAGACTCCAGTTC | 67586 |
rs31986230 | snp | A/G | 0.5 | 0 | intron-variant | Ubxn11 | GRCm38.p3 | 4:134117218 | GGCTTTTCGGGAACA[A/G]GAATCGTGGCAGCAC | 67586 |