SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3658911 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Usp48 | Mm_Celera | 4:137622375 | ATTAAATGCTATAGG[C/T]CTGTCTGTATATAGG | 170707 |
rs3660751 | snp | C/T | 0.5 | 0 | intron-variant | Usp48 | Mm_Celera | 4:137622658 | TCTCTCCAGCCCCTG[C/T]AGTGAATCACATTTC | 170707 |
rs3660867 | snp | C/T | 0.5 | 0 | intron-variant | Usp48 | Mm_Celera | 4:137622710 | AGTGAAAGTATTTGC[C/T]CCAATTCCTGCTGAC | 170707 |
rs3660900 | snp | A/C | 0.5 | 0 | intron-variant | Usp48 | Mm_Celera | 4:137622733 | CTGCTGACCTGGGCA[A/C]TTCCTAGGATCCCCA | 170707 |
rs3661463 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Usp48 | Mm_Celera | 4:137622835 | CCCATTATACACCCA[C/T]GGTAATGATAAATGA | 170707 |
rs3662343 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Usp48 | Mm_Celera | 4:137593635 | CAAAGACTGAGCCTA[C/T]CACTTCGAAGACTAC | 170707 |
rs3662366 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Usp48 | Mm_Celera | 4:137593654 | TTCGAAGACTACAAA[C/T]CCCAGGATGCCTCGC | 170707 |
rs3662387 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Usp48 | Mm_Celera | 4:137593663 | TACAAACCCCAGGAT[A/G]CCTCGCGCTCCGCGA | 170707 |
rs4136290 | snp | C/T | 0.5 | 0 | intron-variant | Usp48 | GRCm38.p3 | 4:137622429 | TCAAAATTAATAAAC[C/T]ATGCAATCAGTGGAA | 170707 |
rs4224856 | snp | A/G | 0.489796 | 0.070696 | utr-variant-3-prime | Usp48 | Mm_Celera | 4:137657274 | TGAGAAGCGCGGGGC[A/G]GAGCCAGGAGAGCTG | 170707 |
rs4224857 | snp | A/T | 0.489796 | 0.070696 | utr-variant-3-prime | Usp48 | Mm_Celera | 4:137657346 | TGCCTTTGGGGACAC[A/T]GGGACTCACGGGACC | 170707 |
rs4224858 | snp | C/T | 0.244898 | 0.249948 | utr-variant-3-prime | Usp48 | Mm_Celera | 4:137657431 | CTCACCAAGAGCCCA[C/T]TCTTTCCCAAGGCCA | 170707 |
rs4224859 | snp | C/T | 0.489796 | 0.070696 | utr-variant-3-prime | Usp48 | Mm_Celera | 4:137657607 | TCCTCCCCCTTTCTC[C/T]TGGCATTGGCTGTGC | 170707 |
rs6315708 | snp | A/T | 0.455 | 0.143091 | intron-variant | Usp48 | Mm_Celera | 4:137626784 | CTCTGTTGAAGTCAT[A/T]TATTTTCTACACTAA | 170707 |
rs13460783 | snp | A/G | | | utr-variant-3-prime | Usp48 | Mm_Celera | 4:137658283 | CGTGCACACTAGAGA[A/G]AATTCTGCATACTGA | 170707 |
rs13460784 | snp | A/G | | | utr-variant-3-prime | Usp48 | Mm_Celera | 4:137657811 | CAGAGCCTTACTGGA[A/G]CTTCAGCTCAGACCC | 170707 |
rs13460785 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Usp48 | Mm_Celera | 4:137658319 | ATCCCCAGCTCTACC[C/T]GTGTATATTTCTAGT | 170707 |
rs13460786 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Usp48 | Mm_Celera | 4:137657876 | TTGGGATCCCTGGGC[C/T]GCGGCTTCCTCACAG | 170707 |
rs13460787 | snp | A/G | | | utr-variant-3-prime | Usp48 | Mm_Celera | 4:137657024 | TAGGGGAGCACGGAC[A/G]GGGCTGGGCAGCGAT | 170707 |
rs13468982 | snp | A/G | | | utr-variant-3-prime | Usp48 | Mm_Celera | 4:137656316 | ATGTCAAATAAAGCA[A/G]ATTGCACTGATGGGC | 170707 |
rs13468983 | snp | G/T | 0.444444 | 0.157135 | synonymous-codon, nc-transcript-variant | Usp48 | Mm_Celera | 4:137637889 | GTATATTTCTGAACC[G/T]AGTAAGTTGTCATGC | 170707 |
rs13468984 | snp | C/T | 0.432133 | 0.171253 | synonymous-codon, nc-transcript-variant | Usp48 | GRCm38.p3 | 4:137608141 | GGATGTTCGGAATGT[C/T]GTGCAGCAGCAGTTC | 170707 |
rs27545955 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | Usp48 | Mm_Celera | 4:137656838 | CGGAGCTCCGTAGGA[C/T]AGCACGGGTTTTCAT | 170707 |
rs27545956 | snp | C/T | 0.48 | 0.0979796 | utr-variant-3-prime | Usp48 | Mm_Celera | 4:137656539 | CAAACTCCAAGTGAC[C/T]GTCTAGAGACAAGAT | 170707 |
rs27545957 | snp | C/T | 0.375 | 0.216506 | utr-variant-3-prime | Usp48 | Mm_Celera | 4:137656486 | TGCCCTGCTCACTAG[C/T]GGATCTGTGTCCCAG | 170707 |
rs27545958 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Usp48 | Mm_Celera | 4:137655968 | AGAATGGATGTCACC[C/T]AGACTTTGTCTGCTG | 170707 |
rs27545959 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp48 | Mm_Celera | 4:137655856 | GCTCCAAGCAAACCA[A/G]AGCAAAAAATTCCTT | 170707 |
rs27545960 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Usp48 | Mm_Celera | 4:137655578 | ACAGCGGTCAGTGCA[G/T]GTAGGTTTCAGTTAT | 170707 |
rs27545961 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp48 | Mm_Celera | 4:137655546 | CTAAGAGTCGGTGGT[A/G]GGAGACTTGCAGAAT | 170707 |
rs27545962 | snp | A/T | 0.475309 | 0.108333 | intron-variant | Usp48 | Mm_Celera | 4:137655486 | ATTTAACCTGCCCGG[A/T]GCCCTATCTGGTGCA | 170707 |
rs27545963 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Usp48 | Mm_Celera | 4:137654979 | GGAGAGAAGACACAG[C/G]TACTGGAGGTCAGCC | 170707 |
rs27545964 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Usp48 | Mm_Celera | 4:137654895 | CATAAAAGTCAGGTC[C/G]TTAAAAAGGAAGGAA | 170707 |
rs27545965 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp48 | Mm_Celera | 4:137654478 | GTTGCTAAGGTGGGG[C/T]AGGTGCTAGAAGAGC | 170707 |
rs27545966 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Usp48 | Mm_Celera | 4:137654344 | GGGTTGCAACAGCCT[C/T]GAACAGGTTACTGGA | 170707 |
rs27545967 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Usp48 | Mm_Celera | 4:137654337 | AATGGAAGGGTTGCA[A/G]CAGCCTTGAACAGGT | 170707 |
rs27545968 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp48 | Mm_Celera | 4:137654320 | TGAACTCTGCAAAGG[A/G]TAATGGAAGGGTTGC | 170707 |
rs27545969 | snp | C/G | 0.495868 | 0.0452663 | intron-variant | Usp48 | Mm_Celera | 4:137654136 | CGTGCCTGGCACCCA[C/G]AACGCCCTCCAAAGT | 170707 |
rs27545970 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Usp48 | Mm_Celera | 4:137654086 | AGGAGGTTTCTGGTT[C/G]TCCATTCTGTAGCCA | 170707 |
rs27545971 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Usp48 | Mm_Celera | 4:137654078 | CTGAGCCAAGGAGGT[G/T]TCTGGTTGTCCATTC | 170707 |
rs27545972 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp48 | Mm_Celera | 4:137653912 | AATGGGCAAATGGTA[A/G]TTAGACCATATATAA | 170707 |
rs27545973 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Usp48 | Mm_Celera | 4:137653754 | AGAAAGCTCTAAAAT[A/G]GCCTACAAATAACTG | 170707 |
rs27545974 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Usp48 | Mm_Celera | 4:137653664 | GTAGACAGTCACATG[A/C]CAGCTGAGGACCAAA | 170707 |
rs27545975 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Usp48 | Mm_Celera | 4:137653612 | CTCTGGTGCCCAGGA[A/C]TGGAGCCCTCAGAAG | 170707 |
rs27545976 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp48 | Mm_Celera | 4:137653569 | TACTGCTAGGAAAGG[A/G]GCAGTTATCTCCTAA | 170707 |
rs27545977 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp48 | Mm_Celera | 4:137653544 | AACAAGCTAACTGGA[A/G]AGAGTGAGTTACTGC | 170707 |
rs27545978 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Usp48 | Mm_Celera | 4:137653521 | CCAGAGGAATCCATG[C/T]CTAGGGAAACAAGCT | 170707 |
rs27545979 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Usp48 | Mm_Celera | 4:137653458 | AAACAGAAGAGTGGC[A/G]GCATGCCTGCAAgtg | 170707 |
rs27545980 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp48 | Mm_Celera | 4:137653441 | ACTACAAAGGTTATA[A/G]CAAACAGAAGAGTGG | 170707 |
rs27545981 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp48 | Mm_Celera | 4:137653231 | GGTACAAAGGTGAAC[C/T]TTGTTAGCCATGTAA | 170707 |
rs27545982 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Usp48 | Mm_Celera | 4:137653222 | GGGGGAACTGGTACA[A/G]AGGTGAACTTTGTTA | 170707 |
rs27545983 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Usp48 | Mm_Celera | 4:137653185 | AGTGGGAAGCAGGGA[A/G]CATAGCCATTGTTTA | 170707 |
rs27545984 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp48 | Mm_Celera | 4:137652853 | ACACAGTAGAAGGGT[A/G]AGAACTATGGGACAG | 170707 |
rs27545985 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp48 | Mm_Celera | 4:137652822 | GGGAGTGTCACTGTG[C/T]TCCCTGGAGGCTGAG | 170707 |
rs27545986 | snp | C/G | 0.459184 | 0.136902 | intron-variant | Usp48 | Mm_Celera | 4:137652772 | GGCCCTGAGGGAACA[C/G]GTGCCTCTTTCCCAA | 170707 |
rs27545987 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Usp48 | Mm_Celera | 4:137652704 | GCTCCTCCTGCAGTG[A/C]CAGCTGTGTGTACAA | 170707 |
rs27545988 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Usp48 | Mm_Celera | 4:137652614 | GAGCAGTGCTCTGCC[A/T]CATACAGTATGCCAT | 170707 |
rs27545989 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Usp48 | Mm_Celera | 4:137652354 | TCAGTGAGCTAAGGT[A/G]GCACAACAGAGCAGG | 170707 |
rs27545990 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Usp48 | Mm_Celera | 4:137652347 | TTCTGGTTCAGTGAG[C/G]TAAGGTGGCACAACA | 170707 |
rs27545991 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Usp48 | Mm_Celera | 4:137652307 | TAAATCCAGAGGTGT[C/T]TGCCCTGGGGTGGGC | 170707 |
rs27545992 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Usp48 | Mm_Celera | 4:137652120 | ACACCTGTCCAGGAT[A/G]GAAATTGGCTTTGGA | 170707 |
rs27545993 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Usp48 | Mm_Celera | 4:137652111 | ACTAAGGTGACACCT[A/G]TCCAGGATGGAAATT | 170707 |
rs27545994 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp48 | Mm_Celera | 4:137652101 | ACCCCAGTGGACTAA[A/G]GTGACACCTGTCCAG | 170707 |
rs27545995 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp48 | Mm_Celera | 4:137652025 | TTGGAATTAGAGCTA[C/T]CCTGTTTCCACGAGT | 170707 |
rs27545996 | snp | G/T | 0.459184 | 0.136902 | intron-variant | Usp48 | Mm_Celera | 4:137651857 | TAGACGTGAGATATA[G/T]TTTGTGTATACCCCA | 170707 |
rs27545997 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Usp48 | Mm_Celera | 4:137651836 | CTGGATTTTTAAGTA[G/T]TTGCATAGACGTGAG | 170707 |
rs27545998 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp48 | Mm_Celera | 4:137651762 | TGGCCTCTGCTGTTG[C/T]GTCCAGGGGTGTGGG | 170707 |
rs27545999 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Usp48 | Mm_Celera | 4:137651738 | CTGGGCAGGCACAGC[A/T]CAGTGGCTTGGCCTC | 170707 |
rs27546000 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Usp48 | Mm_Celera | 4:137651707 | ATTTAATTAGTCCCC[G/T]CTAGGCTGTTTTCTC | 170707 |
rs27546001 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp48 | Mm_Celera | 4:137651238 | GCCTGTGAAAGGATC[A/G]CTTGCTGACTCTTGA | 170707 |
rs27546002 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp48 | Mm_Celera | 4:137651182 | ACAAACCAGGTATGG[A/G]TGTGTGGCTTCCTCC | 170707 |
rs27546003 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Usp48 | Mm_Celera | 4:137650993 | TGCATGCATTTCTTC[C/G]GGTTTGCTTGTTGTA | 170707 |
rs27546004 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Usp48 | Mm_Celera | 4:137650920 | CCCTGGTTTCTGGTT[A/C]TGATTTCTATCGGAG | 170707 |
rs27546005 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Usp48 | Mm_Celera | 4:137650902 | ACTGAGTTCACTTCA[A/G]TGCCCTGGTTTCTGG | 170707 |
rs27546006 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp48 | Mm_Celera | 4:137650853 | GAGGGCAGAAGCCTG[A/G]GTCAGAACCCAGGGT | 170707 |
rs27546007 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Usp48 | Mm_Celera | 4:137650801 | GTTTTTTTCTCTGAC[A/C]AGGGGCCAGCTGCTC | 170707 |
rs27546008 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp48 | Mm_Celera | 4:137650728 | CACTGCTATATAGAC[A/G]GTCAGAATAGACAGC | 170707 |
rs27546009 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp48 | Mm_Celera | 4:137650678 | GACACCTACCCACTC[C/T]TGGTTCTCTCTGGAT | 170707 |
rs27546010 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp48 | Mm_Celera | 4:137650607 | TGGGCCTTGTCCTCC[C/T]AGCCTGCAGTGGTGA | 170707 |
rs27546011 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp48 | Mm_Celera | 4:137650590 | ACCTGCACAGACAGC[A/G]TTGGGCCTTGTCCTC | 170707 |
rs27546012 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Usp48 | Mm_Celera | 4:137650526 | GAGAGAGAGGCTGGG[A/G]CTTTTGCTCTCCTGT | 170707 |
rs27546013 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Usp48 | Mm_Celera | 4:137650491 | AGGATGGACAGTGGT[A/G]ATGAAGGACATGGGT | 170707 |
rs27546014 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Usp48 | Mm_Celera | 4:137650275 | GTGTGTAGACTTTGT[A/T]TCTTCTTCTCCCCAC | 170707 |
rs27546015 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp48 | Mm_Celera | 4:137650019 | GTCTAGGTCGGGGTG[A/G]TCCTGATGAGCTCGG | 170707 |
rs27546016 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Usp48 | Mm_Celera | 4:137649971 | TTTTGAGAGAGAGCG[G/T]GTACTTGGCTGTTGA | 170707 |
rs27546017 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Usp48 | Mm_Celera | 4:137649882 | ATTGCCTCTGGATGT[A/T]ATCACTACAGAAATG | 170707 |
rs27546018 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp48 | Mm_Celera | 4:137649876 | TTCAACATTGCCTCT[A/G]GATGTAATCACTACA | 170707 |
rs27546019 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp48 | Mm_Celera | 4:137649550 | TACTACATGTGCCGA[C/T]AAAGAGAAGAAAGCC | 170707 |
rs27546020 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Usp48 | Mm_Celera | 4:137649536 | TCTCTCCAGCCCTTT[A/C]CTACATGTGCCGACA | 170707 |
rs27546021 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Usp48 | Mm_Celera | 4:137649517 | GTGACTCCTGCGCTG[C/G]GCCTCTCTCCAGCCC | 170707 |
rs27546022 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Usp48 | Mm_Celera | 4:137649422 | CTGTTATGTCAATCC[C/T]TGCTCCACATCTGGG | 170707 |
rs27546023 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Usp48 | Mm_Celera | 4:137649411 | TGGTCACAGGCCTGT[C/T]ATGTCAATCCCTGCT | 170707 |
rs27546024 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Usp48 | Mm_Celera | 4:137649390 | AGGACTTAGCCTCAG[A/C]ATCTCTGGTCACAGG | 170707 |
rs27546025 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Usp48 | Mm_Celera | 4:137649307 | GATGTTACCTTCCCC[A/G]TATGAAATGTGCTGG | 170707 |
rs27546026 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp48 | Mm_Celera | 4:137649235 | ACTTGGTTCTTGTCC[C/T]GGCTCCCGGTGAGAG | 170707 |
rs27546027 | snp | A/C | 0.32 | 0.24 | intron-variant | Usp48 | Mm_Celera | 4:137648970 | TCCAGTAATTCAGTA[A/C]TATGTCTCCTGTTGG | 170707 |
rs27546028 | snp | C/T | 0.32 | 0.24 | intron-variant | Usp48 | Mm_Celera | 4:137648937 | TAAGAAAATCTGTTT[C/T]GCATGGTTGTTAGTT | 170707 |
rs27546029 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Usp48 | Mm_Celera | 4:137648650 | TACTCTGCACAGCAG[C/T]GTAAGCACGTAATTG | 170707 |
rs27546030 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Usp48 | Mm_Celera | 4:137648415 | GTGAGTCAAACAGGA[C/G]TGAAAGAGAGGGCGG | 170707 |
rs27546031 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Usp48 | Mm_Celera | 4:137648359 | GTTATTTCTTTGCGG[C/T]GTGTTTCCTCTCATC | 170707 |
rs27546032 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Usp48 | Mm_Celera | 4:137648357 | GGGTTATTTCTTTGC[A/G]GCGTGTTTCCTCTCA | 170707 |