SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3714509 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Wwp2, Mir140 | Mm_Celera | 8:107549713 | GGGCTGTGTCATCGC[A/G]GATGGAAGAGCCCTT | 66894 |
rs6182031 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wwp2 | Mm_Celera | 8:107464342 | gcagggcttgaactt[A/G]gtgaccttcctcagt | 66894 |
rs6199212 | snp | C/T | 0.5 | 0 | intron-variant | Wwp2 | Mm_Celera | 8:107465253 | AAGGACAGCTTGAGA[C/T]TTGCCACACTCATTC | 66894 |
rs6199777 | snp | A/G | 0.5 | 0 | intron-variant | Wwp2 | Mm_Celera | 8:107465373 | CTCAGATCAGAAAAA[A/G]AAAAAAAAGAAAGAA | 66894 |
rs6200325 | snp | C/G | 0.290657 | 0.246672 | intron-variant | Wwp2 | Mm_Celera | 8:107465475 | AGAACAGACTAGCCA[C/G]TCAGAAGTTAGCCTC | 66894 |
rs6336338 | snp | A/G | 0.5 | 0 | intron-variant | Wwp2 | Mm_Celera | 8:107453135 | TGAAACAATTCAGGA[A/G]TGTAGCATTTGTCTC | 66894 |
rs6336390 | snp | C/T | 0.5 | 0 | intron-variant | Wwp2 | Mm_Celera | 8:107453163 | CTCAGAAGATTATCA[C/T]TCTATAACTAGAGTT | 66894 |
rs6336435 | snp | G/T | 0.5 | 0 | intron-variant | Wwp2 | Mm_Celera | 8:107453188 | AGAGTTCTTGGAAAA[G/T]AANGCAAATAACGGG | 66894 |
rs6336438 | snp | A/G | 0.5 | 0 | intron-variant | Wwp2 | Mm_Celera | 8:107453191 | GTTCTTGGAAAANAA[A/G]GCAAATAACGGGGCT | 66894 |
rs6349621 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Wwp2 | Mm_Celera | 8:107453240 | TTGGCTAAAATGCTC[A/C]GAGATGGTTGATTCC | 66894 |
rs6350055 | snp | A/C/G | 0.5 | 0 | intron-variant | Wwp2 | Mm_Celera | 8:107453302 | atgctctaggtgatc[A/C/G]catccagcctcatag | 66894 |
rs6350648 | snp | C/T | 0.5 | 0 | intron-variant | Wwp2 | Mm_Celera | 8:107453455 | TCGCTCATGTTGGCC[C/T]GGCAGTGAAGCCAGC | 66894 |
rs6350661 | snp | A/G | 0.5 | 0 | intron-variant | Wwp2 | Mm_Celera | 8:107453471 | GGCAGTGAAGCCAGC[A/G]CCTGGTATTTAGCAC | 66894 |
rs6351103 | snp | C/T | 0.5 | 0 | intron-variant | Wwp2 | Mm_Celera | 8:107453516 | GTTGTCCGCCCTGGC[C/T]GCAGCACTCNGTTCT | 66894 |
rs6351118 | snp | A/G/T | 0.5 | 0 | intron-variant | Wwp2 | GRCm38.p3 | 8:107453526 | CTGGCNGCAGCACTC[A/G/T]GTTCTGGAGTAAGGT | 66894 |
rs6409284 | snp | A/C | 0.5 | 0 | intron-variant | Wwp2 | Mm_Celera | 8:107462750 | GGCTTTAAAAACTTT[A/C]TTTTCTGTTGCTCCT | 66894 |
rs13471728 | snp | G/T | | | missense, utr-variant-5-prime | Wwp2 | Mm_Celera | 8:107548548 | GGACCCTCGGACCCA[G/T]GGGATGATACAGGAG | 66894 |
rs13479971 | snp | A/G | 0.32 | 0.24 | intron-variant, downstream-variant-500B | Wwp2, Mir140 | Mm_Celera | 8:107551314 | AGAACCACGGACAGG[A/G]TACTGGAGCACCCTC | 66894 |
rs32563259 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wwp2 | Mm_Celera | 8:107511560 | TTGATTATTGGGATT[A/G]TGTTTTTAAAAGTTT | 66894 |
rs32632003 | snp | A/C | 0.375 | 0.216506 | intron-variant | Wwp2 | Mm_Celera | 8:107518756 | TCCCCCCCCCCCCCC[A/C]CACACACACACACAC | 66894 |
rs32974031 | snp | A/C | 0.375 | 0.216506 | intron-variant | Wwp2 | Mm_Celera | 8:107509867 | CCTTGTTCGTAAATT[A/C]GGGCCAGAGTGTGTA | 66894 |
rs33093758 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wwp2 | Mm_Celera | 8:107499735 | AATAGACAGTGACCG[A/G]CTAAGAGTCTGAGGC | 66894 |
rs33126966 | snp | G/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Wwp2, Mir140 | Mm_Celera | 8:107551226 | TGTGGCTCCCGCCCT[G/T]TGTGTCTCTCTCTGT | 66894 |
rs33551061 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wwp2 | Mm_Celera | 8:107509859 | CTTTATTTCCTTGTT[C/T]GTAAATTCGGGCCAG | 66894 |
rs36256338 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wwp2 | Mm_Celera | 8:107485311 | ACTGTGTGTTAGCAT[C/T]TGGGATGTCTTGGAG | 66894 |
rs36259886 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wwp2 | Mm_Celera | 8:107524671 | TGTACCAGGATGCCT[A/G]AAATGTGGTCACATC | 66894 |
rs36279431 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Wwp2 | Mm_Celera | 8:107540007 | CCCAAGACATCAATG[A/T]CACCGAGAAGTCACC | 66894 |
rs36287897 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wwp2 | Mm_Celera | 8:107486841 | TTTCTCTGCACTAGT[A/G]CTTCATAACTACTTT | 66894 |
rs36303339 | snp | A/G | 0.32 | 0.24 | intron-variant | Wwp2 | Mm_Celera | 8:107547946 | CCAGTCCTGAAACTA[A/G]TTATTGTTGTTCTTT | 66894 |
rs36316413 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Wwp2 | Mm_Celera | 8:107461888 | TCCTTTACCTGCTGA[A/G]GTGTTTCCAGGCCCC | 66894 |
rs36323529 | snp | A/G | 0.244898 | 0.249948 | synonymous-codon | Wwp2 | Mm_Celera | 8:107457564 | CATCGGGAGCTCTGA[A/G]CTGCTCTGGAATGAA | 66894 |
rs36334753 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Wwp2 | Mm_Celera | 8:107546152 | GAAACAGTACCGTAC[A/C]AAAAAAAAAGTGTCA | 66894 |
rs36335744 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wwp2 | Mm_Celera | 8:107530836 | CATCCTTCAGGAAGC[A/G]GCGCTGTGTCACCTT | 66894 |
rs36338264 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Wwp2 | Mm_Celera | 8:107530475 | TACTAGTTACATTGA[A/C]ACAAATTTCTATCTT | 66894 |
rs36345861 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Wwp2 | Mm_Celera | 8:107462613 | CCCCTGCTTTGTTCC[C/T]GGGCTGAGGTTGGAG | 66894 |
rs36347802 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Wwp2 | Mm_Celera | 8:107519451 | CTTCAGTGGATAATT[C/T]GTACAGACATTGGAA | 66894 |
rs36349215 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Wwp2 | Mm_Celera | 8:107467763 | TCACTTGTCTCACAA[A/G]TGGACACTACTCATT | 66894 |
rs36357748 | snp | C/T | 0.32 | 0.24 | intron-variant | Wwp2 | Mm_Celera | 8:107524578 | AATAAGTAAATGTAG[C/T]CCTTAGCCCCTCCAA | 66894 |
rs36372730 | snp | C/T | 0.32 | 0.24 | intron-variant | Wwp2 | Mm_Celera | 8:107546714 | TAAGTCTGCGCTCCG[C/T]CTACAACGCTGGAGC | 66894 |
rs36372819 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wwp2 | Mm_Celera | 8:107458662 | TGCTGGGCTGCCTGG[A/G]AAGGTTAGCTCCTCC | 66894 |
rs36387942 | snp | C/T | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Wwp2, Mir140 | Mm_Celera | 8:107549295 | CTGTAGGGCACTGTT[C/T]CCACGTCTTTGAGTC | 66894 |
rs36393869 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wwp2 | Mm_Celera | 8:107463245 | TGGTCCTCTCTGGGT[C/T]CCCTGTGTCTCTGAG | 66894 |
rs36407210 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Wwp2 | Mm_Celera | 8:107464201 | TCTCGGGCCTCACAT[A/T]GACAAGGGTAGCATC | 66894 |
rs36414971 | snp | G/T | 0.336735 | 0.234472 | intron-variant, nc-transcript-variant | Wwp2, LOC105243277 | Mm_Celera | 8:107447066 | CACCCTTTGTGTCCG[G/T]CAGGCCGAGTCATGA | 66894 |
rs36432724 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Wwp2 | Mm_Celera | 8:107467490 | GACGTCAAGCTGCTG[C/T]ATAGCCATGCAGGCC | 66894 |
rs36441990 | snp | A/G | 0.32 | 0.24 | intron-variant | Wwp2 | Mm_Celera | 8:107523272 | TCTTGAGTAGCTTGC[A/G]ATTAAAGGGTTGTAT | 66894 |
rs36458997 | snp | C/T | 0.32 | 0.24 | intron-variant | Wwp2 | Mm_Celera | 8:107547592 | GAAGGATGCAGTTTA[C/T]AACAGTGGCTCCTGA | 66894 |
rs36478082 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wwp2 | Mm_Celera | 8:107480785 | AAACCAAAGCAAACC[C/T]GTGTGTCATTCATGG | 66894 |
rs36479886 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Wwp2 | Mm_Celera | 8:107526701 | AGGTTTGACTTTGTC[A/G]AGCATGTTGTCTGTT | 66894 |
rs36492492 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Wwp2 | Mm_Celera | 8:107469943 | CCGGGCCTGAGTCAC[A/T]GAGACCTTAGCCTGG | 66894 |
rs36506633 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Wwp2 | Mm_Celera | 8:107462713 | CTCTTGTTGTTCTGA[A/C]GAGCATCTCATAGCC | 66894 |
rs36511955 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Wwp2 | Mm_Celera | 8:107475803 | TCACAGCCATGCCTT[G/T]CCAGCTGACAAGTCT | 66894 |
rs36519992 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Wwp2 | GRCm38.p3 | 8:107555123 | GCCAAAGATTGGGAG[C/T]CCTTGACCTCAGTGC | 66894 |
rs36537376 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wwp2 | Mm_Celera | 8:107476999 | CGAATGCCAAGGGCC[A/G]TACAAGGTTCTAACA | 66894 |
rs36552378 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Wwp2 | Mm_Celera | 8:107547021 | TGAGGGAGAACAGTT[C/T]TGGCTGGGCGTGGCA | 66894 |
rs36560567 | snp | C/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Wwp2, Mir140 | Mm_Celera | 8:107549434 | AAGAAATCAATCGGT[C/T]CCTACATATCCTTTG | 66894 |
rs36613474 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Wwp2 | Mm_Celera | 8:107553920 | TCGTCCTCTGCTGCC[A/G]TCCCAGGAAGGTGAA | 66894 |
rs36646696 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wwp2 | Mm_Celera | 8:107478329 | CTGCTAGGGATTGAA[C/T]TACTTATGGATGCTA | 66894 |
rs36655545 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wwp2 | GRCm38.p3 | 8:107497752 | ACAGCATCTACAGAT[C/T]ACAGGCTTGAGCGTG | 66894 |
rs36668374 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Wwp2 | Mm_Celera | 8:107493415 | GTTTCCAGCATTCTG[C/T]CACCCAGAAACCCAC | 66894 |
rs36672811 | snp | A/G | 0.32 | 0.24 | intron-variant | Wwp2 | GRCm38.p3 | 8:107461382 | GATAATATAACCAGC[A/G]ATTACAGGGTGGGAT | 66894 |
rs36682263 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Wwp2 | Mm_Celera | 8:107506592 | ATTCCATTGACCCAT[C/T]TTCTTTGGCCTCTTT | 66894 |
rs36684705 | snp | A/G | 0.32 | 0.24 | intron-variant | Wwp2 | Mm_Celera | 8:107536908 | CTCAAACTCGGGTGT[A/G]TTCTTAATGATCATG | 66894 |
rs36716269 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wwp2 | Mm_Celera | 8:107461061 | GGGACTTTGGCCTGG[C/T]TGTAGCTATGGAAAG | 66894 |
rs36762693 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wwp2 | Mm_Celera | 8:107489064 | GTTAGAAATGGTCTC[A/G]AAACTCCAGGCTGGA | 66894 |
rs36766273 | snp | A/C/T | 0.132653 | 0.220748 | intron-variant | Wwp2 | GRCm38.p3 | 8:107476070 | AGTGAACACACTAGC[A/C/T]CGCCCCAGGCTGATG | 66894 |
rs36797879 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Wwp2 | Mm_Celera | 8:107495562 | TTGCTGCACGTAGCC[A/G]CAACTCACTCAACTC | 66894 |
rs36852011 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Wwp2 | Mm_Celera | 8:107464673 | TTTAGGAGGCTGAGA[C/T]TGTTGGATCTCTGTG | 66894 |
rs36860818 | snp | G/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Wwp2, Mir140 | Mm_Celera | 8:107550560 | AAGCTACAAATCAGG[G/T]CCAGGCCTCAGCCCT | 66894 |
rs36865759 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Wwp2 | Mm_Celera | 8:107530817 | TAACTTAGGGAACTG[G/T]GTACATCCTTCAGGA | 66894 |
rs36868231 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Wwp2 | Mm_Celera | 8:107457798 | GTAAGATATCAGCAG[G/T]GTAGCTTTCAGCAGC | 66894 |
rs36906357 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Wwp2 | Mm_Celera | 8:107467639 | CCTGCCTTTTCTTCT[A/T]AGGAGCGTCCTGTTG | 66894 |
rs36947905 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Wwp2 | Mm_Celera | 8:107542221 | CTGCCTTCTTCTCTG[A/C]ACTCTCTGACCTTCC | 66894 |
rs36949805 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wwp2 | Mm_Celera | 8:107468682 | TTTGCTGTGATTACC[C/T]TGTGCTACCTACCAC | 66894 |
rs36963317 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wwp2 | Mm_Celera | 8:107471162 | GTGTTCCATGTTCCA[A/G]GGTCTAGATCACCAT | 66894 |
rs37005345 | snp | C/T | 0.32 | 0.24 | intron-variant | Wwp2 | Mm_Celera | 8:107522395 | GGAAGGGTGTAGAGT[C/T]TCCAGGTTGTAAGTG | 66894 |
rs37009312 | snp | A/C | 0.197531 | 0.244432 | intron-variant, upstream-variant-2KB | Wwp2, LOC105243277 | Mm_Celera | 8:107450803 | TTTCACAGTTAGCAA[A/C]ACCCACCTGTCACTC | 66894 |
rs37014550 | snp | C/T | 0.32 | 0.24 | intron-variant | Wwp2 | Mm_Celera | 8:107540307 | TCTCAGTACTATGAT[C/T]CAAGTGCCGGCTTTT | 66894 |
rs37031005 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wwp2 | Mm_Celera | 8:107540609 | ACTGTACTCAGTATG[A/G]CTCCTTGTTTCCAGG | 66894 |
rs37034626 | snp | A/C | 0.32 | 0.24 | intron-variant | Wwp2 | Mm_Celera | 8:107526831 | ACTGCACCATCGGGC[A/C]GTCACAGCAGGGTTT | 66894 |
rs37048210 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Wwp2 | Mm_Celera | 8:107540663 | AGGGAGGTTTTACTA[C/T]GTGGACCACAACACC | 66894 |
rs37065992 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wwp2 | Mm_Celera | 8:107526716 | AAGCATGTTGTCTGT[C/T]AACTAGCTTTTCCAT | 66894 |
rs37132593 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wwp2 | Mm_Celera | 8:107545649 | AAGCCAGCGGGGTTC[A/G]CCTGTGCAGCAGTCA | 66894 |
rs37143332 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Wwp2 | Mm_Celera | 8:107531071 | GAACCCCGGTTGTCA[G/T]ATAACAGTGTACTAT | 66894 |
rs37151719 | snp | C/T | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Wwp2, Mir140 | Mm_Celera | 8:107549299 | AGGGCACTGTTCCCA[C/T]GTCTTTGAGTCTCAG | 66894 |
rs37179821 | snp | C/T | 0.396694 | 0.202437 | intron-variant, upstream-variant-2KB | Wwp2, LOC105243277 | Mm_Celera | 8:107450909 | TTGTCTTCACGTTCT[C/T]TGTCACACACAGTCT | 66894 |
rs37204381 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Wwp2 | Mm_Celera | 8:107546256 | CAAACGGGTTGTTGG[A/G]TTTCATTTCTTGGCT | 66894 |
rs37258658 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wwp2 | Mm_Celera | 8:107457864 | GGCTGTGATGAGTCA[C/T]TTACTTGTTTTCCAG | 66894 |
rs37265376 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Wwp2 | Mm_Celera | 8:107524348 | AGGTGACAGATATCT[A/T]AGACTTTTGGTAGCA | 66894 |
rs37296835 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Wwp2 | Mm_Celera | 8:107537479 | TCACAGAAGAATGGA[C/G]GGACTAGAGGAAGAG | 66894 |
rs37304413 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wwp2 | Mm_Celera | 8:107458121 | AACTTCAGCATGCTT[A/G]GTCCAGGGCTGTAGG | 66894 |
rs37351914 | snp | A/G | 0.32 | 0.24 | intron-variant | Wwp2 | Mm_Celera | 8:107481850 | TGTCTTTTTGGTTAG[A/G]CCCTATGAGTATTTT | 66894 |
rs37368858 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Wwp2 | Mm_Celera | 8:107496047 | AGTTGCCCAAATTCT[C/T]GAGTGCTTATTGGGC | 66894 |
rs37372043 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Wwp2, Mir140 | Mm_Celera | 8:107549659 | GCCCCACTCTGAGAT[A/G]TTTGTCTTGAAGGAG | 66894 |
rs37374045 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Wwp2 | Mm_Celera | 8:107553001 | CGAGGCAGTCCTGCC[A/G]TGTCCTCTTTGATCC | 66894 |
rs37378345 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wwp2 | Mm_Celera | 8:107483266 | TGAATCGGAGGCCGC[C/T]GATTTAAAGAATCCT | 66894 |
rs37379230 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wwp2 | Mm_Celera | 8:107470959 | CATGTCCATTTAGAA[C/T]CCTTCTCTCTGTGCC | 66894 |
rs37420061 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Wwp2 | Mm_Celera | 8:107457585 | CTGGAATGAAATCAT[C/T]GTTCTGTAAGGCTGT | 66894 |
rs37430116 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Wwp2 | GRCm38.p3 | 8:107497171 | GAAGAGAGATCACGT[C/T]AGAATTGTGCCTAAC | 66894 |
rs37469752 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Wwp2 | Mm_Celera | 8:107456700 | TGCCTTGCAGCGTCC[A/G]CGGTAACTCTTGATT | 66894 |