SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3657611 | snp | A/C/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Rnf144b, A930002C04Rik | GRCm38.p3 | 13:47149668 | GCTTTTCTATTTTGC[A/C/G]GCACACGGGTATCAA | 218215 |
rs3657630 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Rnf144b, A930002C04Rik | Mm_Celera | 13:47149680 | TGCGGCACACGGGTA[G/T]CAATACCAACCCAAT | 218215 |
rs3657664 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Rnf144b, A930002C04Rik | Mm_Celera | 13:47149698 | ATACCAACCCAATCA[C/T]CTTCATTCTGCTTCC | 218215 |
rs3658231 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Rnf144b, A930002C04Rik | Mm_Celera | 13:47149773 | TCTCTGTGTAGCTCT[G/T]GCTGTCCTGGAACTC | 218215 |
rs3658918 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Rnf144b, A930002C04Rik | Mm_Celera | 13:47149899 | CAGAGTTTTATAGTG[C/T]GAGGATGGACCGGTT | 218215 |
rs3659488 | snp | A/T | 0.5 | 0 | intron-variant | Rnf144b | Mm_Celera | 13:47134042 | GGGTTCCCTACCAAC[A/T]GTTTTCAGTAGTGCA | 218215 |
rs3659543 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Rnf144b, A930002C04Rik | Mm_Celera | 13:47150030 | GCTTGTCCCTCAGAA[G/T]GCCTTTGGGTACAGC | 218215 |
rs3660811 | snp | C/T | 0.5 | 0 | intron-variant | Rnf144b | Mm_Celera | 13:47134258 | CTGCACAGCCTTCTG[C/T]CCCCATTTTCTTAGC | 218215 |
rs3660829 | snp | C/T | 0.5 | 0 | intron-variant | Rnf144b | Mm_Celera | 13:47134264 | AGCCTTCTGTCCCCA[C/T]TTTCTTAGCAGCAGT | 218215 |
rs3660833 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rnf144b | Mm_Celera | 13:47134270 | CTGTCCCCATTTTCT[C/T]AGCAGCAGTTCTAGC | 218215 |
rs3675111 | snp | A/C | 0.5 | 0 | intron-variant | Rnf144b | Mm_Celera | 13:47134393 | GTTTTTATTATTATT[A/C]GTTTACTTTTACCTC | 218215 |
rs3675672 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Rnf144b | Mm_Celera | 13:47134446 | TTCTACATCCGTTTG[A/G]CAGATAAGCCCTATG | 218215 |
rs3676208 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Rnf144b | Mm_Celera | 13:47134524 | CTAATCAACTTTGCG[A/G]GTTTTCTTTGAAGTT | 218215 |
rs3685503 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf144b | Mm_Celera | 13:47208812 | CTGCCACCCCCGGGC[A/G]GCCATTTTCCTTTGG | 218215 |
rs3685578 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rnf144b | Mm_Celera | 13:47208850 | TGCATTTTGAACTAT[C/T]GGTAGCTATGACCTC | 218215 |
rs4136581 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Rnf144b | Mm_Celera | 13:47237696 | TGACTCTTAGACATT[C/T]ACTGTAGAAATGCCT | 218215 |
rs6165205 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Rnf144b, LOC105245487 | Mm_Celera | 13:47130368 | GGGGAGCCTGAGTTT[C/T]CCCCTACCCCATGGC | 218215 |
rs6165674 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Rnf144b, LOC105245487 | Mm_Celera | 13:47130427 | CACTCTGTTCTAAGT[A/G]TAAAGAGATTATGCT | 218215 |
rs6165726 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Rnf144b, LOC105245487 | Mm_Celera | 13:47130455 | GCTGATCACTTAGAG[C/T]GTTTTCTGTGCATCA | 218215 |
rs6321367 | snp | C/T | 0.5 | 0 | intron-variant | Rnf144b | Mm_Celera | 13:47189680 | ggctggtgtcaatca[C/T]atggcatttctcctg | 218215 |
rs6321864 | snp | A/C | 0.5 | 0 | intron-variant | Rnf144b | Mm_Celera | 13:47189753 | acgtctggTTTGAAA[A/C]CTTNAAATTTGCTTT | 218215 |
rs6321870 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Rnf144b | Mm_Celera | 13:47189757 | ctggTTTGAAANCTT[C/T]AAATTTGCTTTGGCT | 218215 |
rs6321920 | snp | C/T | 0.5 | 0 | intron-variant | Rnf144b | Mm_Celera | 13:47189785 | GCTTTAGTTGGGTAT[C/T]ACTTTTCTATGATTA | 218215 |
rs6321994 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Rnf144b | Mm_Celera | 13:47189821 | TAAGTATCAGTAATC[A/G]GGATTTTGATGTGGC | 218215 |
rs6322450 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Rnf144b | Mm_Celera | 13:47189863 | AAGATCTGAAACTCA[A/G]AACAGGACAGGACCC | 218215 |
rs6356169 | snp | A/G | 0.42 | 0.183303 | intron-variant | Rnf144b | Mm_Celera | 13:47231061 | CTGTGTTCATCCATG[A/G]TAAGTCGATCAAATA | 218215 |
rs6356185 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Rnf144b | Mm_Celera | 13:47231064 | TGTTCATCCATGGTA[A/C]GTCGATCAAATAGTT | 218215 |
rs6369187 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Rnf144b | Mm_Celera | 13:47231187 | GGAAGCTAAGGTTAG[C/T]CTAAGATCACATGAC | 218215 |
rs6369662 | snp | A/T | 0.429688 | 0.173817 | intron-variant | Rnf144b | Mm_Celera | 13:47231246 | GCTTAAGTTGTATAA[A/T]TCTTTACAGTTCTAG | 218215 |
rs6369760 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Rnf144b | Mm_Celera | 13:47231308 | ACAAGGATGGTCTGC[C/T]ATATCCTTCACAGCC | 218215 |
rs6372937 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Rnf144b | Mm_Celera | 13:47231936 | TCTACTTTGAGATAC[C/T]GAAGGCAAATTAACT | 218215 |
rs6373290 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Rnf144b | GRCm38.p3 | 13:47231954 | AGGCAAATTAACTTC[A/G]GCATAATTAAAAATG | 218215 |
rs6373377 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf144b | Mm_Celera | 13:47232011 | TTGATATATATCAGC[C/T]GATAATTAAATTAAA | 218215 |
rs6411221 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Rnf144b, LOC105245487 | Mm_Celera | 13:47129893 | CATTTTAACTGAGAA[A/G]AGATAAGGAACCAAA | 218215 |
rs6411274 | snp | C/T | 0.387812 | 0.208586 | intron-variant, upstream-variant-2KB | Rnf144b, LOC105245487 | Mm_Celera | 13:47129920 | CAAAAGGTGGTAATG[C/T]TATTACACGAGCAAC | 218215 |
rs6412344 | snp | C/T | 0.304688 | 0.243945 | intron-variant, upstream-variant-2KB | Rnf144b, LOC105245487 | Mm_Celera | 13:47130076 | GCACCATCCAGAAAT[C/T]GGTAAGCTCGTTGCC | 218215 |
rs6412896 | snp | A/T | 0.207612 | 0.24638 | intron-variant, upstream-variant-2KB | Rnf144b, LOC105245487 | Mm_Celera | 13:47130148 | ATTAGGAGGGTTCTT[A/T]AAAACttatttattt | 218215 |
rs13463384 | snp | C/G | 0.432133 | 0.171253 | utr-variant-3-prime | Rnf144b | Mm_Celera | 13:47247275 | GGGTTCCTATAGCAA[C/G]CGTTTGGCTGTGACA | 218215 |
rs13481802 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Rnf144b | Mm_Celera | 13:47244222 | ACTCCAAGTGCCATC[A/G]CACTGAGTATTAGGG | 218215 |
rs29222473 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf144b | Mm_Celera | 13:47226754 | ATCCACACACATGTG[A/G]CCGACCTACTATAAA | 218215 |
rs29223620 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Rnf144b | Mm_Celera | 13:47135875 | ACCTTGACTGCAAGT[A/G]TAAGAGGCAACTCAT | 218215 |
rs29224484 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rnf144b | Mm_Celera | 13:47233583 | ATAATATAACAATTA[G/T]CCAGATACCATTGTA | 218215 |
rs29224784 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf144b, LOC105245486 | Mm_Celera | 13:47221152 | CAGTGCCTGTTAACC[C/T]GAGCATAATGAACTC | 218215 |
rs29225085 | snp | A/G | 0.5 | 0 | intron-variant | Rnf144b | Mm_Celera | 13:47229758 | ATAGTCTTGCCGAGC[A/G]TAGTACCAGCCCTAG | 218215 |
rs29225214 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf144b | Mm_Celera | 13:47179950 | GAGGCCCTCCCCACA[A/G]GTGGTGCTTCCTCAT | 218215 |
rs29227810 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rnf144b | Mm_Celera | 13:47215319 | ATGCCCCCACACCCT[G/T]CCTCCTTTATCTTAG | 218215 |
rs29228328 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rnf144b | Mm_Celera | 13:47205148 | ATCTATCTATCTATC[A/T]ATCTATCTATCTATC | 218215 |
rs29228413 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Rnf144b | Mm_Celera | 13:47241018 | GTAAGACCTCAGTCA[C/T]GCTCGTCTTCGGTAG | 218215 |
rs29229442 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rnf144b | Mm_Celera | 13:47179987 | CCAGCCTCCAGACGC[A/C]GAGATGCTACACTCC | 218215 |
rs29231222 | snp | A/G | 0.255 | 0.24995 | intron-variant | Rnf144b | Mm_Celera | 13:47230432 | ACCTTTTCCTCTGTC[A/G]TATTGTTATTGATAA | 218215 |
rs29232037 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rnf144b | Mm_Celera | 13:47233508 | ATTGGAAATGTTTTT[G/T]TTTTTTTGTTTTTTT | 218215 |
rs29232091 | snp | G/T | 0.498615 | 0.0262793 | intron-variant, nc-transcript-variant | Rnf144b, LOC105245487 | Mm_Celera | 13:47127026 | GAGGTCATAAGAAAC[G/T]TAGATAACTATTCCT | 218215 |
rs29232256 | snp | A/C | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Rnf144b, LOC105245486 | Mm_Celera | 13:47226080 | AGCCACATCGCTCAC[A/C]CTTGACATACTTTCC | 218215 |
rs29233293 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf144b | Mm_Celera | 13:47238480 | AAGGAGTCTGTTCCA[C/T]GCGCTGCCATGCGCC | 218215 |
rs29234318 | snp | A/G | 0.42 | 0.183303 | utr-variant-3-prime | Rnf144b | Mm_Celera | 13:47245639 | TTCCTAACTTACTCA[A/G]GAGGGTAGACTCAAA | 218215 |
rs29234700 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Rnf144b, LOC105245487 | Mm_Celera | 13:47122359 | AGTGAATGTGTCTAC[A/G]TTAAAAAAAAAAAGA | 218215 |
rs29235784 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf144b | Mm_Celera | 13:47238343 | AACAAAACAATCAGT[A/G]TTCCCCCGCCAGTTG | 218215 |
rs29236869 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf144b, LOC105245486 | Mm_Celera | 13:47223803 | TCTGTCTTCCTGAAT[C/T]CTCCAGATTGGCTCA | 218215 |
rs29239166 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Rnf144b | Mm_Celera | 13:47216098 | AGTGCTCCCTGCGCT[C/T]GCATAGACAAGGCTG | 218215 |
rs29239210 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rnf144b | Mm_Celera | 13:47211655 | CCGAGAACCTGCGGT[A/T]CTTCTGTCCCAGGTT | 218215 |
rs29240913 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf144b | Mm_Celera | 13:47229706 | GAACGGAAAACTGTA[C/T]CTTTTTAGTACTTGA | 218215 |
rs29241048 | snp | C/T | 0.32 | 0.24 | intron-variant, nc-transcript-variant | Rnf144b, LOC105245487 | Mm_Celera | 13:47127988 | GCGGGCATCCCTTTC[C/T]GCTTCCTGATGGCAG | 218215 |
rs29241141 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rnf144b | Mm_Celera | 13:47233516 | TGTTTTTGTTTTTTT[G/T]TTTTTTTTTAAATTG | 218215 |
rs29242593 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf144b, LOC105245486 | Mm_Celera | 13:47223758 | TTTCCTGGGTAGAAC[C/T]GGCTTGCCCACTTGG | 218215 |
rs29243066 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Rnf144b | Mm_Celera | 13:47179280 | CGCTCCCCAGCATTC[A/C]GCTCTGGAACCCCCT | 218215 |
rs29243804 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Rnf144b, LOC105245487 | Mm_Celera | 13:47126130 | TCTGATTTTCAAAGC[A/G]ATGAGGATTTTGTTC | 218215 |
rs29244787 | snp | G/T | 0.375 | 0.216506 | intron-variant, nc-transcript-variant | Rnf144b, LOC105245487 | Mm_Celera | 13:47123015 | CGCCCTGTGCTGGGT[G/T]TATGGCCAGGGCTCC | 218215 |
rs29251028 | snp | A/G | 0 | 0 | intron-variant | Rnf144b | Mm_Celera | 13:47232905 | TGACAGTCAGGGGGG[A/G]AAAAATCTGTGGAGT | 218215 |
rs29252426 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Rnf144b | Mm_Celera | 13:47234085 | TAACTTTACATGTGC[A/G]CCACTTAGTAAACTT | 218215 |
rs29495395 | snp | A/T | 0.375 | 0.216506 | upstream-variant-2KB, intron-variant | Rnf144b, LOC105245487 | Mm_Celera | 13:47121895 | TAATATATTCCATAA[A/T]TATGCATCATACTCA | 218215 |
rs29495723 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Rnf144b | Mm_Celera | 13:47236391 | CAGAACTGCTCCTGC[A/G]TTGATCATTTCTAGT | 218215 |
rs29496671 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf144b | Mm_Celera | 13:47213665 | TGTAAGTCTATGTGC[C/T]GGCACATGTAGTGTG | 218215 |
rs29496898 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf144b | Mm_Celera | 13:47217105 | AGCTTTTTGCCATGT[C/T]TCTATGGCAGGGGAG | 218215 |
rs29508284 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf144b | Mm_Celera | 13:47227652 | AATGGACTGAATTCA[C/T]CAAGCTTAGTTGGTA | 218215 |
rs29508749 | snp | C/G | 0.359862 | 0.224567 | intron-variant, upstream-variant-2KB | Rnf144b, LOC105245487 | Mm_Celera | 13:47123739 | GTAAGGTCCACATGG[C/G]AGAAAGGCCGTTCTC | 218215 |
rs29509601 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Rnf144b | Mm_Celera | 13:47196215 | CCTGGCTCTTTTTGG[C/T]GTGGCATCGCGCTCC | 218215 |
rs29510709 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Rnf144b | Mm_Celera | 13:47239232 | TTGAACCACTTGGCT[C/T]TGTGTCCCTTTCTGC | 218215 |
rs29512100 | snp | A/C | 0.415225 | 0.187619 | intron-variant | Rnf144b | Mm_Celera | 13:47232412 | AGAGCAGTCTGAAAT[A/C]GCCTTGCTTTGCACA | 218215 |
rs29513306 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Rnf144b, LOC105245486 | Mm_Celera | 13:47226004 | GCTTCTACACGTGCC[A/G]GTTCACTTTCTTTCA | 218215 |
rs29513975 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf144b | Mm_Celera | 13:47212320 | ACAATAAACAATAAG[A/G]CTACCAAAAAGTATT | 218215 |
rs29514619 | snp | A/C | 0.32 | 0.24 | intron-variant | Rnf144b | Mm_Celera | 13:47168987 | GGACGCCCCCCCCCC[A/C]CACACACACACCAGA | 218215 |
rs29515036 | snp | G/T | 0.290657 | 0.246672 | intron-variant | Rnf144b | Mm_Celera | 13:47234150 | CTCGGCCGTGACTCC[G/T]ACCAAAAAGGGGCTT | 218215 |
rs29525077 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf144b | Mm_Celera | 13:47215415 | TGCACTGAGGCAGCA[C/T]TAGTGCAGGGGTAGA | 218215 |
rs29528979 | snp | A/G | 0.487535 | 0.077957 | intron-variant, nc-transcript-variant | Rnf144b, LOC105245487 | Mm_Celera | 13:47127423 | CTGCATAGTCTATAC[A/G]GGATGGGGCTGCACA | 218215 |
rs29533686 | snp | A/G/T | 0 | 0 | intron-variant | Rnf144b | Mm_Celera | 13:47237946 | TGTGTGTGTGTGTGT[A/G/T]TATATATATATATAT | 218215 |
rs29550230 | snp | C/G | 0.5 | 0 | intron-variant | Rnf144b | Mm_Celera | 13:47240490 | TTGCTCCTCTGTCTC[C/G]TAGAGATGGGGTTGC | 218215 |
rs29550871 | snp | A/C | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Rnf144b, LOC105245487 | Mm_Celera | 13:47125092 | ATGATTCAGCCCAGC[A/C]AACTCCGGAGAATCC | 218215 |
rs29551081 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Rnf144b | Mm_Celera | 13:47212932 | GATACCCAAGGCTGG[A/G]CAAATGTTTTTCCCC | 218215 |
rs29552669 | snp | G/T | 0.290657 | 0.246672 | intron-variant | Rnf144b | Mm_Celera | 13:47234254 | GTTCTCCAAAGCTTA[G/T]CGGCCTCAAAGTTTG | 218215 |
rs29553247 | snp | C/T | 0.493827 | 0.0552116 | utr-variant-5-prime, intron-variant | Rnf144b, LOC105245487 | Mm_Celera | 13:47122849 | TGACCCTCCGGGAGT[C/T]TCAGGCTGTGGCTCA | 218215 |
rs29567819 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Rnf144b | Mm_Celera | 13:47216505 | CTATGAGTCTCTTTT[A/G]GACTAGAGTAGGATT | 218215 |
rs29583213 | snp | C/T | 0.375 | 0.216506 | intron-variant, nc-transcript-variant | Rnf144b, LOC105245486 | Mm_Celera | 13:47224202 | ACCTCAGCAGTTCCC[C/T]GCAGCGTTGGAGAAG | 218215 |
rs29588913 | snp | A/G | 0.387812 | 0.208586 | intron-variant, upstream-variant-2KB | Rnf144b, LOC105245487 | Mm_Celera | 13:47125247 | GAGTTACAGTATTGC[A/G]CTACAGGTTCTATCG | 218215 |
rs29589090 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rnf144b | Mm_Celera | 13:47142276 | CTCCTGCTCCTCCTC[A/C]TCATCATCATCATTT | 218215 |
rs29589428 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf144b | Mm_Celera | 13:47217056 | CGACAGTATTGTCTA[C/T]GGCCATAGTTGGCTC | 218215 |
rs29618914 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rnf144b | Mm_Celera | 13:47179923 | TGCTTTGGCCATGAA[C/T]TGAAGCATCGTGAGG | 218215 |
rs29622167 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf144b | Mm_Celera | 13:47179894 | TGTTTTTATCTCTTT[C/T]CTCATAGCCCTTTTG | 218215 |
rs29639577 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf144b | Mm_Celera | 13:47238548 | TTAGCCCCAAGAGCT[A/G]GTTTAAGGGGCTCAG | 218215 |
rs29640485 | snp | C/T | 0.375 | 0.216506 | intron-variant, nc-transcript-variant | Rnf144b, LOC105245486 | Mm_Celera | 13:47224071 | TGCTCTGCAGGCTTT[C/T]CCCATGTATCGGAAC | 218215 |
rs29656769 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Rnf144b | Mm_Celera | 13:47241440 | GTTCCTAAATAAACA[C/T]CCCAGGGGCTTATTT | 218215 |