SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13462496 | snp | C/T | 0.260355 | 0.249785 | synonymous-codon | Ube2g2 | Mm_Celera | 10:77643593 | GATCCTGCTTTCTGT[C/T]GTGAGCATGCTGGCA | 22213 |
rs13462497 | snp | A/C | 0.336735 | 0.234472 | utr-variant-3-prime | Ube2g2 | Mm_Celera | 10:77644564 | TGGGGCTCTGAGGCT[A/C]CCCCTGTGCACACTG | 22213 |
rs29380481 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Ube2g2 | Mm_Celera | 10:77621953 | CATTCATGCCTACAA[A/G]GGGAAAGTTTCACGA | 22213 |
rs36244037 | snp | C/G | 0.197531 | 0.244432 | intron-variant | Ube2g2 | Mm_Celera | 10:77630499 | TGGCAGGAGCACTCT[C/G]AGAGGCAGTCTGCCG | 22213 |
rs36247716 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2g2 | Mm_Celera | 10:77627653 | TTGTTAACCAGTGCA[C/T]ATTGTCCTGAAGACT | 22213 |
rs36295784 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Ube2g2 | Mm_Celera | 10:77639018 | AGCGAATGAGCAAGC[A/G]AGCAACTAAGAGGAC | 22213 |
rs36335917 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2g2 | Mm_Celera | 10:77633930 | TATTTAAATTTAGGA[A/G]TCATTTCTGGAACTT | 22213 |
rs36362736 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Ube2g2 | Mm_Celera | 10:77635160 | CCTCCAGCCCTCCAA[C/T]GGCCTGGTCAGCTGT | 22213 |
rs36375810 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Ube2g2 | Mm_Celera | 10:77644108 | GATGCTCAGTCTGGT[C/G]TTCGGACACTTGGAC | 22213 |
rs36417363 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Ube2g2 | Mm_Celera | 10:77627504 | GGCTATTTAAGCTAC[C/T]TTTAAGAAAAATAGT | 22213 |
rs36448264 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ube2g2 | Mm_Celera | 10:77638082 | CATGCTTCTGGGGCT[A/G]AGAACAACGCAGTAG | 22213 |
rs36461864 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2g2 | Mm_Celera | 10:77633210 | ACCTGGAACCGTGTG[C/T]GTCAGGGCACTGCCA | 22213 |
rs36474982 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Ube2g2 | Mm_Celera | 10:77633196 | CTGCCACCTTGCATA[A/C]CTGGAACCGTGTGCG | 22213 |
rs36477287 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ube2g2 | Mm_Celera | 10:77634993 | GATAGAGGCTTGTCA[C/G]TGGTTATGTTGTCAT | 22213 |
rs36488014 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2g2 | Mm_Celera | 10:77629610 | TTCCTTCTCCTTCCA[C/T]TTGCCATTTTTCCAA | 22213 |
rs36491114 | snp | C/G | 0.32 | 0.24 | intron-variant | Ube2g2 | Mm_Celera | 10:77634359 | GTCAGGGCACCTGAT[C/G]AGTCTGTAATATTTG | 22213 |
rs36496275 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ube2g2 | Mm_Celera | 10:77638178 | CTTGAGCAAATGCCA[C/T]GGAGCCCATTCCAAG | 22213 |
rs36502046 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2g2 | Mm_Celera | 10:77638012 | GTAGTAAGCCTGAGT[A/G]TTCGCAAACAACTTT | 22213 |
rs36541920 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Ube2g2 | Mm_Celera | 10:77643700 | ATAGACTATGTAAGA[C/T]ATGCCAATATATCCT | 22213 |
rs36561223 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2g2 | Mm_Celera | 10:77639217 | GAGAGCTAGTCACTG[C/T]TGTTTTTGAAGTAGC | 22213 |
rs36582576 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Ube2g2 | Mm_Celera | 10:77643261 | GTAATAAGGTAGAAT[C/T]CAGTTGCAACTGGTC | 22213 |
rs36602802 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2g2 | Mm_Celera | 10:77628325 | GTACCAGGGCTCTTA[C/T]CCTTCTGTCTGTCTG | 22213 |
rs36611267 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ube2g2 | Mm_Celera | 10:77644212 | GGCTGCAGTGTCTGG[A/G]GAAGCACGCAGGAGC | 22213 |
rs36646980 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2g2 | Mm_Celera | 10:77626274 | ATGAAATAGAACGGG[C/T]AGTTACAGCTGTTGT | 22213 |
rs36663043 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2g2 | Mm_Celera | 10:77633950 | TTCTGGAACTTGCTG[A/G]TTCTAGATCACACTG | 22213 |
rs36667620 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2g2 | Mm_Celera | 10:77629269 | ATGTCTCTCTGTGGC[C/T]GCGTGTTCTCTCTTG | 22213 |
rs36669247 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Ube2g2 | Mm_Celera | 10:77636708 | TTGAGAACTTCATTC[A/C]CATCACTCATACCCA | 22213 |
rs36673727 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2g2 | Mm_Celera | 10:77630232 | TGGTCTTCAGCAGGT[A/G]ACCTTAAGTGGCTGT | 22213 |
rs36711072 | snp | A/C | 0.32 | 0.24 | intron-variant | Ube2g2 | Mm_Celera | 10:77633416 | AGGAAGAGGACTGGT[A/C]ATTTCTGCCCTGTGA | 22213 |
rs36715378 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Ube2g2 | Mm_Celera | 10:77639109 | CACACCCTGTGAAGG[C/T]GGCCATGCTGCTGCT | 22213 |
rs36771407 | snp | A/G/T | 0.231111 | 0.249285 | intron-variant | Ube2g2 | GRCm38.p3 | 10:77642056 | CAGAGCAGAGGGCAC[A/G/T]CTGTAGTTAGCCTGC | 22213 |
rs36789420 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2g2 | Mm_Celera | 10:77638240 | CAGAGGTGCCAGGTA[C/T]AACGAGGCCCTACAG | 22213 |
rs36797849 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2g2 | Mm_Celera | 10:77637109 | AGCTGTGGAAGAAGC[A/G]TTTAAATACCAAGAA | 22213 |
rs36812295 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Ube2g2 | Mm_Celera | 10:77626197 | TCGGGCCTCTGCACT[C/T]AGCACAGTTGTGCTG | 22213 |
rs36830447 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Ube2g2 | Mm_Celera | 10:77638892 | GTGGGCTTTGCTCAT[A/G]GTGACTCCTCAGTGG | 22213 |
rs36837541 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Ube2g2 | Mm_Celera | 10:77634267 | TCCTGTGTCAACACA[A/G]GCACACCTGCACTTA | 22213 |
rs36844765 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2g2 | Mm_Celera | 10:77634301 | GTATGCCATCAGCGG[C/T]GTGCCTGCCGTAGGA | 22213 |
rs36910835 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ube2g2 | Mm_Celera | 10:77632586 | ATGGTGGATGAGCCT[C/T]AGATAGTGTGTGTGG | 22213 |
rs36926618 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ube2g2 | Mm_Celera | 10:77637952 | TGCATACCTGTTCAG[A/G]TGGCAGGCATGCTGG | 22213 |
rs36938181 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Ube2g2 | Mm_Celera | 10:77644044 | ACTCCTCAGTAGTGC[C/T]TTGGTGTGGAGCTGG | 22213 |
rs36942783 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Ube2g2 | Mm_Celera | 10:77632286 | ACAGCCTGCATGGGA[C/G]CTCAGCTGGCCTGTC | 22213 |
rs36986509 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Ube2g2 | Mm_Celera | 10:77634968 | TTTGATGTCCGGGTC[C/G]TCCCGTGTAGATAGA | 22213 |
rs36996530 | snp | A/G/T | 0.142012 | 0.225474 | intron-variant | Ube2g2 | GRCm38.p3 | 10:77629321 | TCATGCTCTAAGTGC[A/G/T]CGTGTGTGGAAACTA | 22213 |
rs37053335 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Ube2g2 | Mm_Celera | 10:77630593 | GCACTTATCTGGGGA[A/C]CAAGAGGCACCCTTT | 22213 |
rs37059993 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Ube2g2 | Mm_Celera | 10:77637050 | TTATAGAGTTGACCT[C/G]GAATTCCAATGGAGC | 22213 |
rs37201208 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2g2 | Mm_Celera | 10:77627121 | TAGTTTCTTCTCCAT[C/T]TGGTTGTCTCCTCGG | 22213 |
rs37214025 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2g2 | Mm_Celera | 10:77634859 | TGGTATTTTTGGACA[C/T]CGAGGAAGCCTGACA | 22213 |
rs37220359 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2g2 | Mm_Celera | 10:77632463 | AAATGCTGAAGGCCC[A/G]ACCCAGAAGAACAGC | 22213 |
rs37241474 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Ube2g2 | Mm_Celera | 10:77636917 | TTCTGTTAGAATTCA[C/T]TGTAAAGTTCTTATA | 22213 |
rs37242655 | snp | C/T | 0.336735 | 0.234472 | downstream-variant-500B | Ube2g2 | Mm_Celera | 10:77646024 | GCTCACTTGGAATCT[C/T]TGGGAACCTGAGTGA | 22213 |
rs37248334 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ube2g2 | Mm_Celera | 10:77627091 | ATGGATCAGGACCTG[A/G]CCTTACTTGACATGT | 22213 |
rs37343522 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ube2g2 | Mm_Celera | 10:77636789 | AGTCTTCTGGGAGAG[A/G]ACATACATAGGCTGA | 22213 |
rs37344709 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ube2g2 | Mm_Celera | 10:77630355 | AGTCTCCCTGCAGCC[C/T]GAGCTTGGCCTCTCA | 22213 |
rs37360770 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2g2 | Mm_Celera | 10:77628789 | TCCCCTGCTGGACCT[C/T]TCCGTAGTCACGCCC | 22213 |
rs37378487 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ube2g2 | Mm_Celera | 10:77634870 | GACACCGAGGAAGCC[C/T]GACACCTCCTGCTGG | 22213 |
rs37398738 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2g2 | Mm_Celera | 10:77643843 | GAGGTGCTTCAAGAG[C/T]TTACGAACCCAATTA | 22213 |
rs37438455 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ube2g2 | Mm_Celera | 10:77638836 | GTGCCACCGTTTAAC[A/G]TCAGTGATAGATCCT | 22213 |
rs37443470 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ube2g2 | Mm_Celera | 10:77632895 | ATCAGACTCGGCCTG[C/T]TAAACTTTCTTCTTT | 22213 |
rs37450485 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2g2 | Mm_Celera | 10:77633600 | GTGTGCAGTGCGGTA[C/T]AGTTGTGCCTTGTGG | 22213 |
rs37462166 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Ube2g2 | Mm_Celera | 10:77636919 | CTGTTAGAATTCACT[A/G]TAAAGTTCTTATAGT | 22213 |
rs37479611 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2g2 | Mm_Celera | 10:77628803 | TCTCCGTAGTCACGC[C/T]CTCTGTTGTGTGTCT | 22213 |
rs37555229 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Ube2g2 | Mm_Celera | 10:77642657 | GTGCACCACCACCGC[C/T]CATTATAAATGTTTT | 22213 |
rs37614479 | snp | A/G | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Ube2g2, Mir1930 | Mm_Celera | 10:77640981 | TACACAGAAGACATG[A/G]ATGGTGCAGATTGGA | 22213 |
rs37643883 | snp | C/T | 0.35503 | 0.226867 | utr-variant-3-prime | Ube2g2 | Mm_Celera | 10:77644968 | GTCCCAGGAAGCATT[C/T]TGAGCTTCTTTTGAC | 22213 |
rs37718839 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2g2 | Mm_Celera | 10:77637098 | ATCCTGGTTCTAGCT[A/G]TGGAAGAAGCATTTA | 22213 |
rs37729592 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2g2 | Mm_Celera | 10:77632670 | AGGAGCAGCAGCATT[A/G]CACCTGAAGAGCCAA | 22213 |
rs37732437 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2g2 | Mm_Celera | 10:77636986 | TTTAAGATTTTTTAG[C/T]AGTGACTCTGTCTCA | 22213 |
rs37747278 | snp | G/T | 0.244898 | 0.249948 | intron-variant, downstream-variant-500B | Ube2g2, Mir1930 | Mm_Celera | 10:77641696 | CTGTGACCAGTGAGT[G/T]ACGGTGTGAGCACCA | 22213 |
rs37755335 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Ube2g2 | Mm_Celera | 10:77633529 | GCAGCCCTTATTTAT[G/T]TCTCTCAGACCTTAC | 22213 |
rs37767858 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ube2g2 | Mm_Celera | 10:77629053 | GCTGAATGCATCCAC[A/G]ACAGGATGTGCTGTC | 22213 |
rs37804473 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2g2 | Mm_Celera | 10:77634010 | TGCTTTTCTGTGGGA[C/T]GATAGAGGCCTGTAG | 22213 |
rs37817476 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2g2 | Mm_Celera | 10:77625901 | GCTTGAACTGTATGT[C/T]AGTGATTGCAAGTGA | 22213 |
rs37826102 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2g2 | Mm_Celera | 10:77631363 | GTTTCACATCATGGA[C/T]AACACAGCAGGTGTC | 22213 |
rs37859650 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ube2g2 | Mm_Celera | 10:77638972 | GGATGGGGAGCGCCC[A/G]TAGGTGACAGTTACC | 22213 |
rs37875869 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ube2g2 | Mm_Celera | 10:77644358 | AAGTCCACTTTCCTA[C/T]CCATAATGACCCTTG | 22213 |
rs37893352 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Ube2g2 | Mm_Celera | 10:77638636 | GAAAATGTCCAAGCC[C/T]AAGTCTCTATCATTT | 22213 |
rs37914980 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ube2g2 | Mm_Celera | 10:77642215 | CTCTGCCTGGAAGGG[A/G]CCATAATACTGTCCG | 22213 |
rs37933696 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2g2 | Mm_Celera | 10:77629668 | TGGTCATTACCACAC[A/G]GTGTTGGATATGAGT | 22213 |
rs38018045 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ube2g2 | Mm_Celera | 10:77634393 | GGTGGTGGGTCATAT[C/G]CATCCATGGGTGTAG | 22213 |
rs38020635 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Ube2g2 | Mm_Celera | 10:77634090 | CCGTGTACTTTCTCT[C/T]ACTTTTCAGTGCTGG | 22213 |
rs38044810 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Ube2g2, Mir1930 | Mm_Celera | 10:77639705 | CTGTGTGTGAGTTGC[A/G]TGCGTATACATGTAC | 22213 |
rs38133304 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2g2 | Mm_Celera | 10:77637445 | CCTGACCCAGGTTCA[C/T]CTTGCAGCATCTAAC | 22213 |
rs38141465 | snp | C/T | 0.142012 | 0.225474 | intron-variant, upstream-variant-2KB | Ube2g2, Mir1930 | GRCm38.p3 | 10:77640814 | CTCCTGAACTGCTGA[C/T]GTGGGTCACATTAGT | 22213 |
rs38212718 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2g2 | Mm_Celera | 10:77629416 | CTTTCAGTTTCTTTG[A/G]ATGATCTGTTTCCAA | 22213 |
rs38231118 | snp | A/T | 0.32 | 0.24 | intron-variant | Ube2g2 | Mm_Celera | 10:77642317 | TTGATGGAGAGTTTA[A/T]ATTACTCAGGATGGC | 22213 |
rs38292094 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ube2g2 | Mm_Celera | 10:77639014 | CTAGAGCGAATGAGC[A/G]AGCGAGCAACTAAGA | 22213 |
rs38399509 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2g2 | Mm_Celera | 10:77628310 | TACACACATCTATCT[A/G]TACCAGGGCTCTTAC | 22213 |
rs38454239 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2g2 | Mm_Celera | 10:77628181 | TGCTCTGTTCTTTAT[C/T]CAGTCTGTTCCTGTG | 22213 |
rs38455102 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Ube2g2 | Mm_Celera | 10:77627647 | TTATGATTGTTAACC[A/C]GTGCACATTGTCCTG | 22213 |
rs38467452 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ube2g2 | Mm_Celera | 10:77637433 | AGCCTCTGTCTTCCT[C/G]ACCCAGGTTCACCTT | 22213 |
rs38512008 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ube2g2 | Mm_Celera | 10:77643373 | GGCAGGCATCTGGGA[C/T]CTGTGCCAACAGGAA | 22213 |
rs38518672 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Ube2g2 | Mm_Celera | 10:77639078 | AGGCAGCATGAGAGA[C/G]GAAAACTCAGCTGAC | 22213 |
rs38520300 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2g2 | Mm_Celera | 10:77626017 | GACTTTTTCTCGCTG[A/G]ACTGTAGGATCCTGT | 22213 |
rs38662653 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2g2 | Mm_Celera | 10:77630978 | CTAGACATAAGAATC[C/T]CTAAATGTTGAACTC | 22213 |
rs38687258 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ube2g2 | Mm_Celera | 10:77629641 | ATGTGTCCACAGGCT[G/T]TGTTCATTTGTTGGT | 22213 |
rs38694490 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Ube2g2 | Mm_Celera | 10:77634229 | GTGAACTGATGTGTG[G/T]CCTGTCTATTTCATC | 22213 |
rs38764217 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ube2g2 | Mm_Celera | 10:77638570 | CAGGCCCCTTGACCA[A/G]CTTTTCTTTTTAAGG | 22213 |
rs38883859 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Ube2g2 | Mm_Celera | 10:77637961 | GTTCAGATGGCAGGC[A/G]TGCTGGAAAAGAGAA | 22213 |
rs38902023 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2g2 | Mm_Celera | 10:77633229 | AGGGCACTGCCACAC[C/T]TATGCCCAAGCTCTT | 22213 |
rs38981663 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ube2g2 | Mm_Celera | 10:77625922 | TTGCAAGTGAGGCAG[C/T]GGGATCCTTTCACAT | 22213 |