SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3673473 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Ube2h | Mm_Celera | 6:30258625 | TAACTTGTTACTCAC[A/G]GATGCCTAACTATCT | 22214 |
rs3701429 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Ube2h | Mm_Celera | 6:30273156 | TCTGCGTACAAAAAT[A/G]ACTGTGGCACTTGCA | 22214 |
rs3707266 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2h | Mm_Celera | 6:30234257 | TCTGGAAAGGCACCA[A/G]GCACACTTGACTGGT | 22214 |
rs4225750 | snp | A/G | 0.21875 | 0.248039 | utr-variant-3-prime | Ube2h | Mm_Celera | 6:30211526 | CAAGTATCACACAAT[A/G]TGTACCAAATACAAT | 22214 |
rs4225751 | snp | C/T | 0.375 | 0.216506 | utr-variant-3-prime | Ube2h | Mm_Celera | 6:30211630 | CCGTGAGTGGGAAGC[C/T]GCACACCCCTGGCCC | 22214 |
rs4225752 | snp | A/G | 0.21875 | 0.248039 | utr-variant-3-prime | Ube2h | Mm_Celera | 6:30211655 | TGGCCCCCAGGGGCC[A/G]CCTTTCCATCCAATT | 22214 |
rs4225753 | snp | C/T | 0.21875 | 0.248039 | utr-variant-3-prime | Ube2h | Mm_Celera | 6:30211659 | CCCCAGGGGCCGCCT[C/T]TCCATCCAATTCCCA | 22214 |
rs13465478 | snp | A/C | | | utr-variant-3-prime | Ube2h | GRCm38.p3 | 6:30212122 | CATCTCTCCAGCACT[A/C]ATGTGTTTTGTCCAC | 22214 |
rs13470032 | snp | C/T | 0.165289 | 0.235211 | synonymous-codon | Ube2h | GRCm38.p3 | 6:30215025 | GGAAGAGGGCACTGG[C/T]GACAGCTCATCGGAG | 22214 |
rs29973656 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Ube2h | Mm_Celera | 6:30275370 | ACCTGGTCAGAGTTA[C/T]CAGTATGATGATACA | 22214 |
rs30024828 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Ube2h | Mm_Celera | 6:30259206 | CTCCCAATTCCACAG[C/T]TTAGTATCTGTACGC | 22214 |
rs30064204 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2h | Mm_Celera | 6:30269094 | CACAAAACCCTGTAA[A/G]TCAGGAGCAGTGACA | 22214 |
rs30070302 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Ube2h | Mm_Celera | 6:30241878 | ATTGGGTAAATCCCT[A/G]AGTCTACTTTACTGT | 22214 |
rs30105365 | snp | A/T | 0.375 | 0.216506 | intron-variant | Ube2h | Mm_Celera | 6:30260751 | CTGTAGACCCATGAA[A/T]TCCCACGCCCCTGTG | 22214 |
rs30168522 | snp | A/C | 0.359862 | 0.224567 | intron-variant | Ube2h | Mm_Celera | 6:30279284 | AAAAAGTTTCATGTA[A/C]AAAAACTACTAAAAT | 22214 |
rs30170479 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2h | Mm_Celera | 6:30302455 | TATCTAGCGTAATAC[C/T]CTTTCTTACTGGCTT | 22214 |
rs30316598 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Ube2h | Mm_Celera | 6:30229573 | GCACAGGCAAAAATC[C/T]CAATACACTTCGAGA | 22214 |
rs30323282 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ube2h | Mm_Celera | 6:30290704 | CTGCACGCCTTTAAT[A/C]CCAGCACTTGGGAGG | 22214 |
rs30421763 | snp | A/T | 0.32 | 0.24 | intron-variant | Ube2h | Mm_Celera | 6:30283722 | TCACAGAGCTCTTTG[A/T]ATTTGTTGTGCCTGC | 22214 |
rs30461693 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2h | Mm_Celera | 6:30248064 | GGGCTAGTCACTTCA[C/T]TTCCAAGCATGGGTC | 22214 |
rs30464804 | snp | A/G | 0.5 | 0 | intron-variant | Ube2h | Mm_Celera | 6:30216501 | ACTGGAGAGAGCGGC[A/G]CCAGAGCAAGCAAAG | 22214 |
rs30515112 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2h | Mm_Celera | 6:30218391 | CCTCAGCAAGCTGAT[A/G]CCACTCAACAAAGAT | 22214 |
rs30520511 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ube2h | Mm_Celera | 6:30235727 | TTTGCTTAACAGCAT[G/T]TGCTATCATGCCCGA | 22214 |
rs30562380 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2h | Mm_Celera | 6:30296075 | TGGAAACGAACCCAG[C/T]TGCAGCCTTCCCTCA | 22214 |
rs30612174 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2h | Mm_Celera | 6:30277186 | GAACTGTCAAACTGT[A/G]CGCATACACGTTTGT | 22214 |
rs30763928 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2h | Mm_Celera | 6:30218552 | AGCTATCTCTCCAGT[C/T]CCACTAGCATAGGTG | 22214 |
rs30804192 | snp | G/T | 0.465374 | 0.126941 | intron-variant | Ube2h | Mm_Celera | 6:30282411 | CAACAACAGAAACAT[G/T]ACCAACTGCCCAGAG | 22214 |
rs30953484 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Ube2h | Mm_Celera | 6:30263905 | TATAATATTTAAAGG[C/T]GAATGCCAAACTGAC | 22214 |
rs31000175 | snp | C/G | 0.375 | 0.216506 | intron-variant | Ube2h | Mm_Celera | 6:30251425 | CATGCCCTGATGTTA[C/G]AGATACAAGCAGTTG | 22214 |
rs31002038 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2h | Mm_Celera | 6:30281993 | AACAGAAGGAAAAAA[A/G]AAAAGCAGCAGGAAA | 22214 |
rs33863554 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2h | Mm_Celera | 6:30268760 | TCCTGTGGCTCACAC[C/T]TACCTCACACCTACC | 22214 |
rs36257108 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Ube2h | Mm_Celera | 6:30294597 | CAGCTTTGAATTGGT[C/T]CTAAGGATCAGAATG | 22214 |
rs36258049 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Ube2h | Mm_Celera | 6:30277489 | AGGAAAATGACTCTA[C/T]ATGCATAGGATTCTC | 22214 |
rs36284446 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2h | Mm_Celera | 6:30218503 | TCTCCCGGGTTTTCT[A/G]CTCATGCTAATGAGG | 22214 |
rs36287251 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Ube2h | Mm_Celera | 6:30261051 | AACTGTATCTCCAAA[C/T]CAATAAATAAACCCA | 22214 |
rs36291317 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Ube2h | Mm_Celera | 6:30239453 | ATGCAAACATGGCTT[A/T]GGTGGGCATCTGAGA | 22214 |
rs36295003 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Ube2h | Mm_Celera | 6:30267807 | ACAGTACACACTGAG[A/G]CCTGTTTAAAGCAAC | 22214 |
rs36298126 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ube2h | Mm_Celera | 6:30262080 | CCCAAAGCCATGCAG[C/T]GCCTGTTGATAGCTC | 22214 |
rs36306239 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ube2h | Mm_Celera | 6:30254364 | TTTAGACTGGTTTTG[A/G]TACATAAGTGAGCTT | 22214 |
rs36314875 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2h | Mm_Celera | 6:30278655 | AGTCTATGCTTCTGA[C/T]CAGCCCTCTCTTTTC | 22214 |
rs36318924 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Ube2h | Mm_Celera | 6:30265745 | CTGCAGTTGACTAAA[C/G]AGAACACAGACACTA | 22214 |
rs36335610 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ube2h | Mm_Celera | 6:30271000 | AGATTAATGAGATCA[C/T]CTTACGCAGCTTCTG | 22214 |
rs36335751 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2h | Mm_Celera | 6:30257826 | TGTGCTCAATGGTGG[C/T]GCAGCTACTGCAGGT | 22214 |
rs36337049 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2h | Mm_Celera | 6:30239498 | ATGAGGAAACGTGAA[C/T]AAAGGAACCAGTCTT | 22214 |
rs36348467 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2h | Mm_Celera | 6:30285150 | TATTTCTCTTATACA[C/T]GCCAAAAATTCAGAA | 22214 |
rs36367475 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Ube2h | Mm_Celera | 6:30259449 | CGATTCCAACTGACG[A/C]CACCCTCCTCTGAAG | 22214 |
rs36384124 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Ube2h | Mm_Celera | 6:30257810 | ACTGCCCCTTTACAC[A/G]TGTGCTCAATGGTGG | 22214 |
rs36385047 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Ube2h | Mm_Celera | 6:30263425 | TGACGTTTACCATTT[A/C]ATCTGCCTGCATCTA | 22214 |
rs36396816 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Ube2h | Mm_Celera | 6:30267556 | CCAACCTTTTTGACG[C/T]TGTAATGTCTGTTGT | 22214 |
rs36412365 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Ube2h | Mm_Celera | 6:30262260 | ATTACACAGCTCATG[A/C]AAGAACTACAGCTAG | 22214 |
rs36417649 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Ube2h | Mm_Celera | 6:30270470 | GGGATCAGGAAGTGA[A/G]TGTCTAAGGAAAACA | 22214 |
rs36424363 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Ube2h | Mm_Celera | 6:30233205 | AAACAGCTGAGCATC[G/T]GTAACACATGGCACC | 22214 |
rs36431972 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2h | Mm_Celera | 6:30254014 | ACTTCAGACAGAAGC[A/G]CTAACACGAATATCA | 22214 |
rs36437575 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ube2h | Mm_Celera | 6:30262012 | AAAGCTAAGTGCGTG[A/G]CTGACAAAGGTCTCT | 22214 |
rs36440824 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Ube2h | Mm_Celera | 6:30270294 | TTTTGTTTTCTTCTG[C/T]TTACATTCTCTTTTG | 22214 |
rs36455893 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ube2h | Mm_Celera | 6:30231984 | GTGGTATACACAATA[A/G]TTACACTAAAGCTTT | 22214 |
rs36457705 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2h | Mm_Celera | 6:30273168 | AATAACTGTGGCACT[C/T]GCATGACTTGGTAGT | 22214 |
rs36461844 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Ube2h | Mm_Celera | 6:30276827 | TGCAACACTGACTTC[A/C]GATGTACAAGCCATA | 22214 |
rs36462373 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Ube2h | Mm_Celera | 6:30296086 | CCAGCTGCAGCCTTC[A/C]CTCAGGATCAAGCAA | 22214 |
rs36479434 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Ube2h | Mm_Celera | 6:30263391 | AAGGCTGCAATAAAA[C/G]AGCAAACCATTTTCA | 22214 |
rs36482001 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Ube2h | Mm_Celera | 6:30276410 | GTTATTTGAAACAGA[A/C]TATGTACAAGTGGTT | 22214 |
rs36482114 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ube2h | Mm_Celera | 6:30293095 | AAACACTTGCTAACT[C/T]AATGCTCCAGGACCC | 22214 |
rs36499135 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ube2h | Mm_Celera | 6:30264297 | TGAAAATTACCACAC[A/G]CAGTAATGCTTGTAT | 22214 |
rs36499500 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2h | Mm_Celera | 6:30262276 | AAGAACTACAGCTAG[C/T]ATCCAAGACACGCCA | 22214 |
rs36507861 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ube2h | Mm_Celera | 6:30297938 | ACATAATCTTGCTGT[A/G]TAGCTTAGGATGGAC | 22214 |
rs36510032 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ube2h | Mm_Celera | 6:30259534 | CCTACGTAGAGCATC[A/G]AGTTCTGAGAATGTA | 22214 |
rs36512769 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ube2h | Mm_Celera | 6:30240004 | CCACCTAGAGACAAA[C/T]TGGACACACTTAACA | 22214 |
rs36512981 | snp | A/C | 0.32 | 0.24 | intron-variant | Ube2h | Mm_Celera | 6:30277905 | ACTTAAAGTTAAAAT[A/C]GCCTCATGAAAGGCA | 22214 |
rs36529983 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Ube2h | Mm_Celera | 6:30255440 | TTGACCCTACTATAC[C/T]AAGTTTTTCTTTCCT | 22214 |
rs36530227 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2h | Mm_Celera | 6:30255353 | GTCTTATATATAAAA[C/T]TTCTAACATCTATAG | 22214 |
rs36547842 | snp | A/C | 0.32 | 0.24 | intron-variant | Ube2h | Mm_Celera | 6:30274602 | CTCATCTAAGCCCCA[A/C]TGCTGTCTCATAAGG | 22214 |
rs36549102 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Ube2h | Mm_Celera | 6:30265268 | CAGTCTGAGGCCACA[A/G]TATCTTAAAAACAAT | 22214 |
rs36553919 | snp | G/T | 0.32 | 0.24 | intron-variant | Ube2h | GRCm38.p3 | 6:30295653 | TAAGCCCAGGGCCTA[G/T]TTTTGTACACACATG | 22214 |
rs36556239 | snp | A/G | 0.277778 | 0.248452 | utr-variant-3-prime | Ube2h | Mm_Celera | 6:30211880 | AAAGGGTCACATGCC[A/G]CTTAAAATCCAATGC | 22214 |
rs36569099 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ube2h | Mm_Celera | 6:30295614 | ATGTAGTGCTTCAGA[C/T]CTTGCCTGGCATGCA | 22214 |
rs36569716 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2h | Mm_Celera | 6:30296702 | GCTGTAGAGTGGTGG[A/G]TAGACTGACCAGGGC | 22214 |
rs36586684 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Ube2h | Mm_Celera | 6:30229071 | GTGTTCTGTTCTACC[A/C]TGGGCAGTCAACAGC | 22214 |
rs36588193 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ube2h | Mm_Celera | 6:30256955 | GTGAAATAGAACTGA[C/G]CATCCGCCTACAGCT | 22214 |
rs36596672 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Ube2h | Mm_Celera | 6:30249957 | TTGTTCCTGACACTC[A/G]GGCAACCAGAGTTAG | 22214 |
rs36599944 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Ube2h | Mm_Celera | 6:30272606 | TGTTGGAGGCACCCG[A/C]TTAAGTATCTGCACA | 22214 |
rs36600063 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ube2h | Mm_Celera | 6:30294577 | ACACACTCAGGCTAC[A/G]GCCTCAGCTTTGAAT | 22214 |
rs36607096 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ube2h | Mm_Celera | 6:30268084 | GTCTAACGTGATGTC[A/G]AGAACAGCAGCTTCT | 22214 |
rs36627492 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2h | Mm_Celera | 6:30259374 | GCCTCCCAAAATGCC[C/T]AAAGTGCATCCTAAT | 22214 |
rs36627911 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Ube2h | GRCm38.p3 | 6:30262019 | AGTGCGTGACTGACA[A/C]AGGTCTCTTCACTCG | 22214 |
rs36628961 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Ube2h | Mm_Celera | 6:30227651 | AATTTGAAACCACAA[C/T]TAGCCATCATTACAG | 22214 |
rs36630372 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ube2h | Mm_Celera | 6:30274574 | CCATTCTAAACACCT[A/G]TGGCCTGTTTGTCTC | 22214 |
rs36649062 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2h | Mm_Celera | 6:30282532 | TACTACCATATTTCA[C/T]CACATGTACAACACA | 22214 |
rs36650075 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ube2h | Mm_Celera | 6:30227146 | ATTAAACACTAAAAG[A/G]TCCACACTGACTCTG | 22214 |
rs36654144 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ube2h | Mm_Celera | 6:30287012 | ACTCTGCAAGATGCT[C/G]AATACAACTTTTTAG | 22214 |
rs36662018 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2h | Mm_Celera | 6:30254423 | TAAGAGGGTAAATTG[C/T]ACTTGGAAATTAGGG | 22214 |
rs36669809 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2h | Mm_Celera | 6:30299266 | AAACTTATTCTTTCA[C/T]CTCACCAACTCAAGA | 22214 |
rs36676472 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2h | Mm_Celera | 6:30273191 | TTGGTAGTGGCATGC[C/T]TTGGATCCCAATATG | 22214 |
rs36676781 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2h | Mm_Celera | 6:30286781 | ACACTAGGCACCTAT[A/G]TGACAGCCAGGTGCT | 22214 |
rs36680272 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Ube2h | Mm_Celera | 6:30240183 | GGAATATCTATTGAG[A/T]CTGTGGAGCGGACTT | 22214 |
rs36688376 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Ube2h | Mm_Celera | 6:30232646 | AGATTTAAATAAAAA[A/T]AATCAGAGCTCCTCG | 22214 |
rs36699187 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2h | Mm_Celera | 6:30285071 | GACCAGGCCGAGATC[C/T]ACATGCTCCACCACA | 22214 |
rs36710500 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2h | Mm_Celera | 6:30270939 | AGTGCTGGCAGGGGC[C/T]ATGGCCACCAAGACC | 22214 |
rs36716440 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Ube2h | Mm_Celera | 6:30216111 | TTCTGAACGAAGTTT[A/G]TAGACCTGAGACTCA | 22214 |
rs36719148 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2h | Mm_Celera | 6:30262372 | CTAAGCTTTGGCTTC[A/G]GAGAGGTCAGCGATA | 22214 |
rs36720913 | snp | A/C | 0.32 | 0.24 | intron-variant | Ube2h | Mm_Celera | 6:30283758 | TCTTTTTAGCAATAG[A/C]AAAGTTAAACCTAAG | 22214 |