SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs27450557 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Usp50 | Mm_Celera | 2:126785456 | CAGTTACAAAGAACC[C/T]GTAAAGCAGGGCTGC | 75083 |
rs27450558 | snp | G/T | 0.459184 | 0.136902 | upstream-variant-2KB | Usp50 | Mm_Celera | 2:126785337 | GCTGTGTCTTGGCAG[G/T]TGAGAATGCTCCATG | 75083 |
rs27450559 | snp | A/G | 0.459184 | 0.136902 | upstream-variant-2KB | Usp50 | Mm_Celera | 2:126785295 | GTTGGAAGGTAAGGA[A/G]TTCTGTGTGATGTAA | 75083 |
rs27450560 | snp | A/T | 0.456747 | 0.140554 | upstream-variant-2KB | Usp50 | Mm_Celera | 2:126784289 | TGCCTCTGGAGTGCC[A/T]AGTTGCTGCTGGCCT | 75083 |
rs27450561 | snp | A/G | 0.152778 | 0.230321 | upstream-variant-2KB | Usp50 | Mm_Celera | 2:126784270 | AGCACCCGTGCTGGG[A/G]CCTTGCCTCTGGAGT | 75083 |
rs27450562 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Usp50 | Mm_Celera | 2:126783809 | GGGCACATACCCATA[A/G]TACACAGGCTGTTAG | 75083 |
rs27450563 | snp | C/T | 0.459184 | 0.136902 | upstream-variant-2KB | Usp50 | Mm_Celera | 2:126783677 | CACTGCTCCCATGAA[C/T]CCTAGAGGGACATCT | 75083 |
rs27450564 | snp | G/T | 0.473373 | 0.11227 | upstream-variant-2KB | Usp50 | Mm_Celera | 2:126783595 | AGCTCTCCCTCTATT[G/T]CTGGGTTTCTCACAC | 75083 |
rs27450565 | snp | C/T | 0.408163 | 0.193609 | upstream-variant-2KB | Usp50 | Mm_Celera | 2:126783478 | ATCACAATTGTCACC[C/T]TTCATACCAAGGTTC | 75083 |
rs27450566 | snp | A/G | 0.124444 | 0.216185 | missense | Usp50 | Mm_Celera | 2:126783277 | TGAGACGCCATGTCA[A/G]TGAAGCACATCAGGC | 75083 |
rs27450567 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp50 | Mm_Celera | 2:126783051 | GTCACGGAGGCCCTG[A/G]GCTGACTGATCAGGG | 75083 |
rs27450568 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Usp50 | Mm_Celera | 2:126782858 | GCCTCCTTGATCTGC[A/G]CAGCTCCCTCTTATC | 75083 |
rs27450569 | snp | A/G | 0.42 | 0.183303 | intron-variant | Usp50 | Mm_Celera | 2:126782802 | GGGACTGGAGCATCT[A/G]CCCAGCATGCAGAGA | 75083 |
rs27450570 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Usp50 | Mm_Celera | 2:126781536 | CCAAGGGCAAGCACA[C/T]AGTGATGCAGGAGAA | 75083 |
rs27450571 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Usp50 | Mm_Celera | 2:126781211 | GAATGACATAAATGT[G/T]TGAATGTCTGACATA | 75083 |
rs27450572 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Usp50 | Mm_Celera | 2:126781158 | CAAACTCACTCTCTA[C/T]CAAGGACAGAAGGAG | 75083 |
rs27450573 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Usp50 | Mm_Celera | 2:126780645 | TCAGACCCTGGCAAC[C/T]TCTGAAATAAAAGTG | 75083 |
rs27450574 | snp | C/G | 0.165289 | 0.235211 | intron-variant | Usp50 | Mm_Celera | 2:126780625 | AGCATGAGTGCTAGT[C/G]CCGCTCAGACCCTGG | 75083 |
rs27450575 | snp | C/T | 0.375 | 0.216506 | missense | Usp50 | Mm_Celera | 2:126779996 | GCGCATCTTGCTGTG[C/T]CTTTTTCAGAAAAGC | 75083 |
rs27450576 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Usp50 | Mm_Celera | 2:126779250 | CTGAATGTCTGAGCA[A/C]ATCTGGAGTAATTTT | 75083 |
rs27450577 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Usp50 | Mm_Celera | 2:126779224 | TGTTGAACCAGTTGG[A/G]CTATGATCCTCTGAA | 75083 |
rs27450578 | snp | A/C/G | 0.444444 | 0.157135 | intron-variant | Usp50 | GRCm38.p3 | 2:126779087 | ATTTGTGAAAAAGAA[A/C/G]CAGTGTTTAGACACT | 75083 |
rs27450579 | snp | A/C | 0.375 | 0.216506 | intron-variant | Usp50 | Mm_Celera | 2:126778916 | AGGCAGGGGGCTGGA[A/C]CTAGCTTGTTAAGGC | 75083 |
rs27450580 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Usp50 | Mm_Celera | 2:126777735 | GCTTTGAGGCATAAT[A/G]CAGCCCTTTCCTACT | 75083 |
rs27450581 | snp | A/G/T | 0.489796 | 0.070696 | intron-variant | Usp50 | GRCm38.p3 | 2:126776064 | GCTGTGCAAATGTGC[A/G/T]TCTGGGAATTTTTCT | 75083 |
rs27450582 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp50 | Mm_Celera | 2:126776015 | AAGAGACCCGTCTTT[C/T]ATACACACAACCAAA | 75083 |
rs27450583 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Usp50 | Mm_Celera | 2:126775976 | CAGGAGAATGGTTGG[C/T]TTGAGACCAGCCTGT | 75083 |
rs27450584 | snp | C/T | 0.165289 | 0.235211 | synonymous-codon | Usp50 | Mm_Celera | 2:126775765 | CGGCACCTTGGAAAT[C/T]GTGGTCCTCACAGCT | 75083 |
rs27450585 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp50 | Mm_Celera | 2:126772798 | TAAAACTAATGAATG[C/T]AATCATGGAACCTGG | 75083 |
rs27450586 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Usp50 | Mm_Celera | 2:126771889 | ATGGTAAAGAACCAT[C/T]GGAGAGCTTTCTGAC | 75083 |
rs27450587 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp50 | Mm_Celera | 2:126771813 | ACACTGCCCCCACAC[A/G]TAGGCATTCACGTAT | 75083 |
rs27450588 | snp | C/G | 0.375 | 0.216506 | intron-variant | Usp50 | Mm_Celera | 2:126771086 | TTCGATCTGAGGCAG[C/G]AAAGTTACCAGATAA | 75083 |
rs27450589 | snp | A/C | 0.375 | 0.216506 | intron-variant | Usp50 | Mm_Celera | 2:126770846 | ACTTTTTAGAAAATC[A/C]TGTTCATGGGGCTGG | 75083 |
rs27450590 | snp | C/T | 0.32 | 0.24 | intron-variant | Usp50 | Mm_Celera | 2:126770304 | CCAAGTCAAATCACC[C/T]TCACTTCTTTCTCTC | 75083 |
rs27450591 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Usp50 | Mm_Celera | 2:126770070 | CGAGGGAGGTCCACA[C/G]GCCTGAACACATTCC | 75083 |
rs27450592 | snp | C/T | 0.32 | 0.24 | intron-variant | Usp50 | Mm_Celera | 2:126769825 | GATAGGGCCAGACAA[C/T]GGGTGTTCTCTCCTT | 75083 |
rs27450593 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp50 | Mm_Celera | 2:126769789 | CGTGCACGTGGCCAA[A/G]ATGCTAGGCCTCCAG | 75083 |
rs27450594 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Usp50 | Mm_Celera | 2:126769775 | ACCTGACCTCTGGCC[A/G]TGCACGTGGCCAAGA | 75083 |
rs27450595 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Usp50 | Mm_Celera | 2:126769553 | GAATGGCTGCTGCTC[A/G]GGTGGCTCCTGTGGG | 75083 |
rs27450596 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp50 | Mm_Celera | 2:126769231 | CCAGGGAGTGCGAAA[A/G]ACCAATGACTGACAG | 75083 |
rs27450597 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Usp50 | Mm_Celera | 2:126769005 | AGTCAGAAACCGATA[C/T]AATGAGAAGTTAACT | 75083 |
rs27450598 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Usp50 | Mm_Celera | 2:126768621 | GCAGCTGAAGTGTGC[A/G]CTATAGGTCAGAGGT | 75083 |
rs27450599 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Usp50 | Mm_Celera | 2:126766640 | TTCAGATCTAGACTG[A/C]GGAGAGGGATGAATG | 75083 |
rs27450600 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Usp50 | Mm_Celera | 2:126766551 | ATCAGATGTCACACA[C/T]TGATACCAGCTTTTT | 75083 |
rs27450601 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Usp50 | Mm_Celera | 2:126766154 | GACCTGTTGTCTGAA[C/T]GCAGTGTGCTAGAGA | 75083 |
rs27450602 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Usp50 | Mm_Celera | 2:126765853 | AGAACCAAGCAGCAA[A/G]TGTAGAGCTTCGAAG | 75083 |
rs27450603 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Usp50 | Mm_Celera | 2:126765314 | ACCCTGTTCTTACTG[C/T]GTGGATGTGCTCACT | 75083 |
rs27450604 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Usp50 | Mm_Celera | 2:126764834 | CAGCAGTGCTCTTAA[C/T]GGTTCAAAGCACTCA | 75083 |
rs27450605 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Usp50 | Mm_Celera | 2:126764808 | ATCTTGCTAATATCC[C/G]AGAACTACCACAGCA | 75083 |
rs27450606 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Usp50 | Mm_Celera | 2:126764690 | GCTTTGGAAAGCCTG[C/T]GTTTACTGTGTGCAT | 75083 |
rs27450607 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Usp50 | Mm_Celera | 2:126764629 | GAGTAGGGACTTAGG[C/T]AAGCACAGCTCCTCT | 75083 |
rs27450608 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Usp50 | Mm_Celera | 2:126764589 | TGGAGGCAGCTAGAA[A/C]GGCCCAGTGGGAGGC | 75083 |
rs27450609 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Usp50 | Mm_Celera | 2:126764447 | CTTGACTTGTTTTCA[C/G]ACACAAACCAGACCA | 75083 |
rs27450610 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Usp50 | Mm_Celera | 2:126763631 | ACTGACAACAAAAAA[A/G]TGATGCTCCAACATA | 75083 |
rs27450611 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Usp50 | Mm_Celera | 2:126763579 | ATCCCAAGTACCTCT[C/T]AGTGACTGAAATGTG | 75083 |
rs27450612 | snp | A/T | 0.493827 | 0.0552116 | intron-variant | Usp50 | Mm_Celera | 2:126763253 | ATATGGTTCAAGACC[A/T]GCCTGGGCTATAAGA | 75083 |
rs27450613 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Usp50 | Mm_Celera | 2:126762725 | GAGGTAGGTGGGAAC[C/T]AGAGCACTGGAACTG | 75083 |
rs27450614 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Usp50 | Mm_Celera | 2:126761793 | TTATACTGAGGAGAT[A/C]ATTTTCTCAAGTCTT | 75083 |
rs27450615 | snp | A/T | 0.18 | 0.24 | downstream-variant-500B | Usp50 | Mm_Celera | 2:126760855 | CTGTGTGTCTATGTG[A/T]ACCATGTGGGTGCTG | 75083 |
rs29502422 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp50 | Mm_Celera | 2:126763197 | ACTTCTACTCAAAAC[C/T]ACAAGGAATCCAGGT | 75083 |
rs29540491 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp50 | Mm_Celera | 2:126774923 | AAGGGTTCACCCTTC[C/T]GTGTCACCATTCATC | 75083 |
rs29542800 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Usp50 | Mm_Celera | 2:126784084 | TTTCCTCCAACAAGG[C/T]CACACCTCCTAATAG | 75083 |
rs29558399 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp50 | Mm_Celera | 2:126765618 | ACCTCTATCACCAAT[C/T]TCTTATTTATTTAAA | 75083 |
rs29562055 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp50 | Mm_Celera | 2:126768240 | CTCAAAGAGCAAATA[A/G]ATAAAAATGTTCAAT | 75083 |
rs29563311 | snp | A/T | 0.5 | 0 | intron-variant | Usp50 | Mm_Celera | 2:126782270 | GGGTTCTAGAACGAA[A/T]AGCTAAGGCTACACA | 75083 |
rs29624358 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp50 | Mm_Celera | 2:126772280 | CTCTCCTATATGTGT[A/G]TACCATGTGACTGCC | 75083 |
rs29680693 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Usp50 | Mm_Celera | 2:126768390 | CAACCACATGGTGGC[G/T]CACAGGCATCTCCAA | 75083 |
rs29763800 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp50 | Mm_Celera | 2:126768739 | GTCACCTTTTTACTA[A/G]CACCATGCACTAGAA | 75083 |
rs29771372 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Usp50 | Mm_Celera | 2:126784039 | TGTAGTTAGGAGAAA[A/G]GAATCATTGCCCACC | 75083 |
rs29820299 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp50 | Mm_Celera | 2:126767742 | GTGCGTGCTCTGACA[A/G]AAGGGCCATGTTTGG | 75083 |
rs29917063 | snp | A/T | | | intron-variant | Usp50 | GRCm38.p3 | 2:126765108 | CTTCTGGTGTGTCTG[A/T]AGACAGCTACAGTGT | 75083 |
rs29934402 | snp | C/T | 0.444444 | 0.157135 | downstream-variant-500B | Usp50 | Mm_Celera | 2:126760571 | TTAGAGCTTGGGTTT[C/T]GACTCATAAACTTAA | 75083 |
rs29954880 | snp | C/G | 0.375 | 0.216506 | intron-variant | Usp50 | Mm_Celera | 2:126773897 | CTAACTTTGTGGGAA[C/G]GTCTCTCAGATTTCA | 75083 |
rs29958965 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp50 | Mm_Celera | 2:126768139 | TTAATTCCAGCACTT[A/G]GGAGGCAGAGGCAGG | 75083 |
rs32818059 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp50 | Mm_Celera | 2:126774924 | AGGGTTCACCCTTCT[A/G]TGTCACCATTCATCA | 75083 |
rs32837626 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp50 | Mm_Celera | 2:126763499 | ACTAGTAGGTAACTA[C/T]CCAAGAAAAATGAAA | 75083 |
rs32905548 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp50 | Mm_Celera | 2:126773753 | CCTGGCCTCTCAACA[A/G]TGCTGAGCCTCAGCT | 75083 |
rs32957391 | snp | G/T | 0.375 | 0.216506 | intron-variant | Usp50 | Mm_Celera | 2:126768792 | CCCCTGGACTCATCA[G/T]TGATGTGCCACAAGT | 75083 |
rs33016017 | snp | G/T | 0.375 | 0.216506 | intron-variant | Usp50 | Mm_Celera | 2:126768408 | CAGGCATCTCCAATG[G/T]AATCTGACTCTCTCT | 75083 |
rs33040245 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp50 | Mm_Celera | 2:126764485 | GCACGATAGTATACA[C/T]GCCTGAAATGCCAGC | 75083 |
rs33055341 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp50 | Mm_Celera | 2:126764139 | ACATTAGTATGCTTT[A/G]GAACAGTGCCACCCA | 75083 |
rs33084206 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp50 | Mm_Celera | 2:126782510 | ACAGATATACGTGCA[C/T]ACACACACACACACA | 75083 |
rs33114885 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp50 | Mm_Celera | 2:126768409 | AGGCATCTCCAATGG[A/G]ATCTGACTCTCTCTT | 75083 |
rs33128637 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp50 | Mm_Celera | 2:126764198 | AGTGAGGTGGTAGAA[C/T]CTTTAGAGATGGGGA | 75083 |
rs33186902 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp50 | Mm_Celera | 2:126767976 | CAGCATTTGAGGGGT[A/G]AAGGCAAGTCACCAG | 75083 |
rs33194497 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp50 | Mm_Celera | 2:126782729 | TAAATTGTCAGCAAA[A/G]CATTCATATACATAA | 75083 |
rs33299280 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp50 | Mm_Celera | 2:126765492 | GGTGAAGATAACCGT[A/G]ACCTGGTCCTGCCTC | 75083 |
rs33421890 | snp | C/T | 0.375 | 0.216506 | utr-variant-3-prime | Usp50 | Mm_Celera | 2:126761191 | GGAAAGGAGAATTAA[C/T]TCCACAAGTTATCCT | 75083 |
rs33453277 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp50 | Mm_Celera | 2:126773945 | TCCTTTTAATCATTA[C/T]TAATGGTAGGCATAA | 75083 |
rs33458098 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp50 | Mm_Celera | 2:126767599 | TCAAAGGACAAAATG[C/T]GATGGTTCCAGAGAG | 75083 |
rs33489566 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Usp50 | Mm_Celera | 2:126768718 | GGTGAATGTAGCTGG[G/T]TTCTAGTCACCTTTT | 75083 |
rs33592052 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp50 | Mm_Celera | 2:126773971 | CATAATGTGTTATAC[A/G]GTGTGTAAAGTTTAC | 75083 |
rs33597271 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp50 | Mm_Celera | 2:126773762 | TCAACAATGCTGAGC[C/T]TCAGCTGCTCTCTGT | 75083 |
rs33644428 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp50 | Mm_Celera | 2:126768428 | TGACTCTCTCTTCCG[A/G]TGTGTCTGAAGACAA | 75083 |
rs33652087 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp50 | Mm_Celera | 2:126763948 | AGATTCTTTTAAGAA[C/T]ACTGAAGATGTTCTA | 75083 |
rs33655222 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp50 | Mm_Celera | 2:126764335 | TTCCCCAGATACTAA[A/G]CTTGAACCTAGGCAT | 75083 |
rs33681493 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp50 | Mm_Celera | 2:126765107 | TCTTCTGGTGTGTCT[A/G]TAGACAGCTACAGTG | 75083 |
rs33688508 | snp | A/C | 0.444444 | 0.157135 | upstream-variant-2KB | Usp50 | Mm_Celera | 2:126784619 | TCTAGGCCTTTTAGT[A/C]GTAAGCCACACACTG | 75083 |
rs33748860 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp50 | Mm_Celera | 2:126768959 | ATAGTCTAAATATAA[A/G]CTCCATTTTCTCTGT | 75083 |
rs45902141 | snp | A/C | | | intron-variant | Usp50 | Mm_Celera | 2:126773584 | ACAATTGATCCCTTG[A/C]AAACTTACAATCTCA | 75083 |