SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3664350 | snp | G/T | 0.5 | 0 | intron-variant | Vprbp | GRCm38.p3 | 9:106814875 | TTTCTCTGTACCCTC[G/T]CCCCCAAACCTGCAC | 321006 |
rs3664809 | snp | C/T | 0.5 | 0 | intron-variant | Vprbp | GRCm38.p3 | 9:106814903 | CACCTGTAGCATGAC[C/T]TCTGGGATGCCCAAA | 321006 |
rs3706273 | snp | C/G | 0.415225 | 0.187619 | intron-variant | Vprbp, Manf | Mm_Celera | 9:106872480 | TGAGCCTGCAGAGGG[C/G]CTGAAGTTATGATCT | 321006 |
rs3706802 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Vprbp, Manf | GRCm38.p3 | 9:106872551 | GTTTATCTTTTATTT[A/G]TGTGAGCTTGACTGT | 321006 |
rs3707428 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Vprbp, Manf | GRCm38.p3 | 9:106872676 | TGTAATTGAAGTGAT[C/T]ACACATGAACACACA | 321006 |
rs3722160 | snp | G/T | 0.5 | 0 | intron-variant | Vprbp | Mm_Celera | 9:106814552 | GGGAATTGAACTCAG[G/T]ACCTCTGGAAGAACA | 321006 |
rs4137867 | snp | A/G | 0.5 | 0 | intron-variant | Vprbp | GRCm38.p3 | 9:106814967 | TCACTAGGGGATCAA[A/G]TAGGGTGGAGTGGGG | 321006 |
rs6172136 | snp | A/T | 0.5 | 0 | intron-variant | Vprbp, Manf | GRCm38.p3 | 9:106874931 | TTCACCCTACCCCAC[A/T]TCTTGTTCAGAACTC | 321006 |
rs6172737 | snp | C/G | 0.492188 | 0.0620098 | intron-variant | Vprbp, Manf | Mm_Celera | 9:106875045 | TAATCAGCTTTAAGA[C/G]TGGGCAAACATTGTA | 321006 |
rs6173232 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Vprbp, Manf | Mm_Celera | 9:106875079 | TTGACATGTCTCTGT[C/T]GCCACGAGCGTGCCA | 321006 |
rs6173273 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Vprbp, Manf | GRCm38.p3 | 9:106875104 | GTGCCACTGTTGGCA[A/G]TTCTGGCTGCGGTCC | 321006 |
rs6173890 | snp | A/G | 0.5 | 0 | intron-variant | Vprbp, Manf | Mm_Celera | 9:106875245 | CTGTGTCTGATAATA[A/G]CAGCCACGTAGCACN | 321006 |
rs6174325 | snp | A/G | 0.5 | 0 | intron-variant | Vprbp, Manf | GRCm38.p3 | 9:106875260 | NCAGCCACGTAGCAC[A/G]GAGGGCTGttnaaat | 321006 |
rs6174353 | snp | C/G | 0.5 | 0 | intron-variant | Vprbp, Manf | GRCm38.p3 | 9:106875271 | GCACNGAGGGCTGtt[C/G]aaatanaattaaatt | 321006 |
rs6174360 | snp | G/T | 0.5 | 0 | intron-variant | Vprbp, Manf | GRCm38.p3 | 9:106875277 | AGGGCTGttnaaata[G/T]aattaaattaaaaat | 321006 |
rs6207241 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Vprbp, Manf | GRCm38.p3 | 9:106876833 | TCCTGGGCAGCAGTG[A/G]CCATATGGTTCATTG | 321006 |
rs13461135 | snp | C/T | | | utr-variant-3-prime, intron-variant | Vprbp, Manf | Mm_Celera | 9:106880710 | CAGAGCGGGAATGGG[C/T]GGCATGGCCTGAGCA | 321006 |
rs29588953 | snp | C/G | 0.5 | 0 | intron-variant | Vprbp | GRCm38.p3 | 9:106829634 | GAACTCAAAAGATGT[C/G]CTGGCCTCTGCTTCT | 321006 |
rs29590371 | snp | A/T | 0.5 | 0 | intron-variant | Vprbp | Mm_Celera | 9:106843581 | AGCAGTCAGTGCTCT[A/T]AACCGCTGAGCAATC | 321006 |
rs29591011 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Vprbp | Mm_Celera | 9:106819051 | TCGAACTCAGAAATC[C/T]GCCTGCCTCTGCCTC | 321006 |
rs29593094 | snp | A/T | 0.5 | 0 | intron-variant | Vprbp | GRCm38.p3 | 9:106847515 | TAGCCTTGAATTTCC[A/T]GTGTAGATTGACTGG | 321006 |
rs29593788 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Vprbp | GRCm38.p3 | 9:106866409 | ACTCCCATGTGAACA[A/G]TGGTAACAGAAAAGA | 321006 |
rs29595071 | snp | C/T | 0.455 | 0.143091 | intron-variant | Vprbp, Manf | Mm_Celera | 9:106879178 | GCCTTTGTAGGCTTC[C/T]GAGGGCTGGAGGAAG | 321006 |
rs29598894 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Vprbp | Mm_Celera | 9:106828557 | AAAAAGTAACCTAGT[A/G]TGGTGACTTCATAGT | 321006 |
rs29601010 | snp | A/G/T | 0.48 | 0.0979796 | intron-variant | Vprbp | GRCm38.p3 | 9:106850081 | TGCATACACAGCAAG[A/G/T]TTTTGCTGAAAGGAC | 321006 |
rs29601575 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Vprbp | GRCm38.p3 | 9:106823294 | TGCCTTGAAACTCAG[C/T]TTAGACTAGCCTGGC | 321006 |
rs29637248 | snp | A/G | 0.5 | 0 | intron-variant | Vprbp, Manf | Mm_Celera | 9:106872130 | TGAGCAGTTAACATA[A/G]CACCTCAGCCGTGAA | 321006 |
rs29637804 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Vprbp | Mm_Celera | 9:106864201 | AAGGCTACTAATTTT[C/T]AACACAACAAATTTG | 321006 |
rs29638970 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Vprbp | Mm_Celera | 9:106824480 | AAGTATGAATTAAAT[A/G]ATGCATACCCACTAT | 321006 |
rs29639496 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Vprbp, Manf | Mm_Celera | 9:106877871 | GGTCGCAGTGGTGTT[C/T]GACAAGCGGTGTTCC | 321006 |
rs29640005 | snp | A/G | 0.5 | 0 | intron-variant | Vprbp | GRCm38.p3 | 9:106816096 | ATGAACAGAGGCCAT[A/G]GAGAAACCTTGCTTG | 321006 |
rs29643264 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Vprbp | GRCm38.p3 | 9:106861292 | CACTGAATCTAGTAT[C/T]TTAGACAACAACAAC | 321006 |
rs29643851 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Vprbp | Mm_Celera | 9:106845909 | AAGGCGTGCGCCACC[A/T]CGCCCGGCTGGCTCA | 321006 |
rs29686268 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | Vprbp | Mm_Celera | 9:106821893 | CACACCCGCGCGCGC[C/T]GAGTGCGCGCGCGAC | 321006 |
rs29688409 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Vprbp | Mm_Celera | 9:106816969 | ACAGAGATATAATTA[C/T]GTAGGAGTGCCCTCT | 321006 |
rs29690088 | snp | A/C | 0.375 | 0.216506 | intron-variant | Vprbp | Mm_Celera | 9:106827264 | ATGCTAAAGTTGAAC[A/C]GCCATGAGTTTAAGT | 321006 |
rs29690135 | snp | A/G | 0.455 | 0.143091 | intron-variant | Vprbp, Manf | GRCm38.p3 | 9:106878843 | TTACCAGTTCCAGAC[A/G]GGCATGGTGTATTTT | 321006 |
rs29690884 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Vprbp | Mm_Celera | 9:106865263 | GGATATGTGTAGTCC[A/G]AGAGAAACAATGAGA | 321006 |
rs29691282 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Vprbp, Manf | GRCm38.p3 | 9:106876983 | ATATTTTGCTTCATG[A/G]CCCAGGTTGGCCTCA | 321006 |
rs29732691 | snp | A/C | 0.432133 | 0.171253 | intron-variant | Vprbp | Mm_Celera | 9:106860262 | ACATACATGCACAGT[A/C]AGTAAATTATGAAAA | 321006 |
rs29737809 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Vprbp | GRCm38.p3 | 9:106863589 | GGTCACTCTTACCCT[C/T]ATAAAACAAGATCTC | 321006 |
rs29738247 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Vprbp, Manf | GRCm38.p3 | 9:106870675 | CTGTCTGAGAAGAAA[A/G]ACCAAGTGACTAGTG | 321006 |
rs29742596 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Vprbp | Mm_Celera | 9:106836744 | TTTTTTTGTTTTTTG[G/T]TTTTTGAGACAGGGT | 321006 |
rs29744665 | snp | C/T | 0.432133 | 0.171253 | intron-variant, downstream-variant-500B, utr-variant-3-prime | Vprbp, Manf | GRCm38.p3 | 9:106868942 | ATATTTAACAGAAAG[C/T]GATGAACCGTACATC | 321006 |
rs29787017 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Vprbp | Mm_Celera | 9:106841741 | TATGTGAGTACAGCA[A/G]AAGAGGGCATCAGAT | 321006 |
rs29793004 | snp | A/G | 0.5 | 0 | intron-variant | Vprbp | GRCm38.p3 | 9:106834788 | AGACAGGGTTCCTCT[A/G]TATAGCCCTGGCTGT | 321006 |
rs29794426 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Vprbp | Mm_Celera | 9:106832519 | GGGACCTTTGGAAGA[A/G]CAGTTGGCGCTCTTA | 321006 |
rs29828886 | snp | C/T | 0.5 | 0 | intron-variant, downstream-variant-500B, utr-variant-3-prime | Vprbp, Manf | GRCm38.p3 | 9:106868866 | CTCTACTTACACACA[C/T]GCAAGCACATGCACG | 321006 |
rs29834525 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Vprbp, Manf | GRCm38.p3 | 9:106872136 | GTTAACATAACACCT[C/T]AGCCGTGAACCTTTA | 321006 |
rs29837702 | snp | A/T | 0.5 | 0 | intron-variant | Vprbp | Mm_Celera | 9:106836273 | GTTATTAGGATAACT[A/T]CTTTTTATATGGGTT | 321006 |
rs29838866 | snp | A/T | 0.432133 | 0.171253 | intron-variant | Vprbp | Mm_Celera | 9:106841969 | AATCCTTGTTCCAAA[A/T]TTTTTTTTATTATTA | 321006 |
rs29839758 | snp | C/T | 0.375 | 0.216506 | intron-variant | Vprbp | Mm_Celera | 9:106825377 | AAATGTGGGCACTAC[C/T]ACAACACATTCATGC | 321006 |
rs29840736 | snp | G/T | 0.46281 | 0.131194 | intron-variant | Vprbp | GRCm38.p3 | 9:106861768 | TATTGATTTCTTACC[G/T]TTTTTTAGATTAAAT | 321006 |
rs29841036 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Vprbp | Mm_Celera | 9:106860785 | ATTCTCATTATTTGG[A/G]ATCTGCTCTGGTGGA | 321006 |
rs29842985 | snp | C/T | 0.5 | 0 | intron-variant | Vprbp | Mm_Celera | 9:106864122 | GTGAGTGCTAGGAAT[C/T]GAATCCAGGTCCTCT | 321006 |
rs29843684 | snp | A/G | 0.5 | 0 | intron-variant | Vprbp | GRCm38.p3 | 9:106835009 | CGGATAGATAGAAAG[A/G]TTCTTTCTGTCTGTT | 321006 |
rs29876064 | snp | C/T | 0.5 | 0 | intron-variant | Vprbp | Mm_Celera | 9:106829410 | TAATGCATGTACACA[C/T]ACACACACACACACA | 321006 |
rs29877267 | snp | A/G | 0.5 | 0 | intron-variant | Vprbp | Mm_Celera | 9:106850219 | AGAGAAAGTATCCAA[A/G]GAGCTAAAGAGATCT | 321006 |
rs29879100 | snp | A/G | 0.48 | 0.0979796 | upstream-variant-2KB | Vprbp | Mm_Celera | 9:106813484 | TTCAGCCTGGCCTGA[A/G]GTTTCAGTAGTCACT | 321006 |
rs29879102 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Vprbp | GRCm38.p3 | 9:106819677 | GCACTTGGAATGCAG[A/G]GGCAGGGGAATGTCT | 321006 |
rs29881085 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB | Vprbp | GRCm38.p3 | 9:106812307 | GAGAGGCAGTGGAAC[C/T]GTAGTTCAATGGGTG | 321006 |
rs29885104 | snp | C/T | 0.455 | 0.143091 | intron-variant | Vprbp, Manf | GRCm38.p3 | 9:106873814 | AGCAGTGGCTTGAGA[C/T]ATCTGTGAGGCAGGG | 321006 |
rs29890434 | snp | G/T | 0.465374 | 0.126941 | intron-variant, downstream-variant-500B, utr-variant-3-prime | Vprbp, Manf | GRCm38.p3 | 9:106869069 | ATGAGCCTGTCACCC[G/T]CTAGAGTTTATATCA | 321006 |
rs29891464 | snp | G/T | 0.432133 | 0.171253 | intron-variant | Vprbp | GRCm38.p3 | 9:106864493 | TTAGTAAAGTTTCAC[G/T]CTTCTGTCTCCCCTG | 321006 |
rs29926954 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Vprbp | Mm_Celera | 9:106816551 | CACCTGGCCCAGCCC[A/G]TTCTGGAACTTCTCT | 321006 |
rs29929213 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Vprbp, Manf | GRCm38.p3 | 9:106873845 | TTTCTCTTTAAGGGC[C/T]ATAAGGGCTGTATGC | 321006 |
rs29930433 | snp | C/T | 0.5 | 0 | intron-variant | Vprbp, Manf | GRCm38.p3 | 9:106879629 | CCTCAGCCCTGTCCC[C/T]TTGTAGCCCAGTGCC | 321006 |
rs29932331 | snp | A/T | 0.5 | 0 | intron-variant | Vprbp | GRCm38.p3 | 9:106825940 | CCACTTCATAGTTCT[A/T]GTTCTAGGATATCCT | 321006 |
rs29937136 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Vprbp | GRCm38.p3 | 9:106841110 | AAGGAAGGGATTTGA[A/G]TTTTATGTAAGGCAG | 321006 |
rs29942418 | snp | C/T | 0.5 | 0 | intron-variant | Vprbp | Mm_Celera | 9:106817405 | GTAGCTGTCTTCAGA[C/T]GCACCAGAAGAGGGC | 321006 |
rs29944799 | snp | C/T | 0.375 | 0.216506 | intron-variant | Vprbp | Mm_Celera | 9:106818023 | CATCTCTCCAGCACC[C/T]CCCCCCCCAACCCTT | 321006 |
rs29967130 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Vprbp | Mm_Celera | 9:106827022 | CAGCAATCTGGAGGA[A/G]CAGTCAATGCTCTTA | 321006 |
rs29982477 | snp | A/G | 0.42 | 0.183303 | intron-variant | Vprbp | GRCm38.p3 | 9:106852176 | CACGTGTAACAAGCT[A/G]TTGTTGGATTGAAGT | 321006 |
rs29982505 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Vprbp | GRCm38.p3 | 9:106852145 | GTTCATAAGATATAA[C/T]ACATAACACATAATG | 321006 |
rs29982509 | snp | A/C | 0.5 | 0 | intron-variant | Vprbp | GRCm38.p3 | 9:106861313 | CAACAACAACAAAAA[A/C]CAAAACCAGAGACTC | 321006 |
rs29983716 | snp | A/T | 0.375 | 0.216506 | upstream-variant-2KB | Vprbp | GRCm38.p3 | 9:106812505 | TTCTTAATTATATGG[A/T]CTGATTTACAAAGTA | 321006 |
rs29985738 | snp | C/T | 0.5 | 0 | intron-variant | Vprbp | Mm_Celera | 9:106857762 | TGTTCCTGTAATATC[C/T]TGACATGAGTCTTCT | 321006 |
rs29987023 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Vprbp, Manf | GRCm38.p3 | 9:106877210 | ACTCTTTTAAGTTAC[A/G]AGAATATTGTTACTA | 321006 |
rs29991240 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Vprbp | GRCm38.p3 | 9:106814230 | CATACGGTAAGAGCC[C/T]AGTATACCCTTTGCA | 321006 |
rs30027228 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Vprbp | GRCm38.p3 | 9:106820255 | TGAGTGTAATTAAAA[C/T]ATTTGATTTAGGGAT | 321006 |
rs30027999 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB | Vprbp | GRCm38.p3 | 9:106812380 | GTCAGGGTATAACAT[C/T]CTCCTCCCCTTCTCT | 321006 |
rs30028760 | snp | A/C | 0.465374 | 0.126941 | intron-variant | Vprbp, Manf | GRCm38.p3 | 9:106870375 | AAACCACACAAAACA[A/C]TTAACCAGGTATGGC | 321006 |
rs30030495 | snp | A/C | 0.387812 | 0.208586 | intron-variant | Vprbp | GRCm38.p3 | 9:106839853 | GAAAAACTTAAAAAA[A/C]GAGATCCTTAAAAGC | 321006 |
rs30033654 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | Vprbp | GRCm38.p3 | 9:106820479 | TGCTATAGAGTCTAA[A/G]TAAATAATGGTCATT | 321006 |
rs30034206 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Vprbp | Mm_Celera | 9:106817527 | ACTGAGCCATCTCGC[C/G]AGCCCCAGATTTTTT | 321006 |
rs30037285 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Vprbp | Mm_Celera | 9:106840837 | GGTGGTTATGAGCCA[C/T]CATGTGGTTGCTGGG | 321006 |
rs30037908 | snp | C/G | 0.5 | 0 | intron-variant | Vprbp | Mm_Celera | 9:106824730 | GTTTGCAATACCAAG[C/G]GGCCTCTCTTCCCAG | 321006 |
rs30039139 | snp | A/C | 0.475309 | 0.108333 | intron-variant | Vprbp | Mm_Celera | 9:106854021 | CAGATTATTTTCTAG[A/C]GTTTCCAGTATATTC | 321006 |
rs30040871 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Vprbp | Mm_Celera | 9:106843299 | CAAAAGAAAGAGTAG[A/G]AACTTAAAGAAACAA | 321006 |
rs30061320 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Vprbp | Mm_Celera | 9:106816189 | CACAATGGGCTGGAC[C/T]CTTCAATAGCAATCA | 321006 |
rs30083320 | snp | A/T | 0.5 | 0 | intron-variant | Vprbp | GRCm38.p3 | 9:106816600 | TTGAACTTAATATCC[A/T]TCTACTTTTTGTTTT | 321006 |
rs30084775 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Vprbp | Mm_Celera | 9:106824775 | GCCATCTTCTGCTAC[A/G]TATGCAGCTAGAAAT | 321006 |
rs30086069 | snp | C/T | 0.5 | 0 | intron-variant | Vprbp | GRCm38.p3 | 9:106866212 | GCTTGTTATAGTGTC[C/T]GTTTGGGGCTTCAAG | 321006 |
rs30087942 | snp | C/T | 0.5 | 0 | intron-variant | Vprbp | GRCm38.p3 | 9:106816059 | GGGTAGGAAATCAGA[C/T]CAGGAACCTGGAAGT | 321006 |
rs30088138 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Vprbp | Mm_Celera | 9:106831597 | AAAATTGCTAATAGT[A/T]CTTTTCAATTGAGAT | 321006 |
rs30088146 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Vprbp, Manf | Mm_Celera | 9:106870750 | GATCCCTTTTCTTTT[C/T]TTTTTTTTTTCCACT | 321006 |
rs30092455 | snp | A/G | 0.5 | 0 | intron-variant | Vprbp | Mm_Celera | 9:106840810 | CAGAAGAGGGCACCA[A/G]ATCTCATTATAGGTG | 321006 |
rs30094319 | snp | C/G | 0.456747 | 0.140554 | intron-variant | Vprbp | GRCm38.p3 | 9:106866603 | CAAGGCAGGTTTATA[C/G]TGTAGATGCCTGTTG | 321006 |
rs30121085 | snp | C/T | 0.5 | 0 | intron-variant | Vprbp | Mm_Celera | 9:106834980 | TAATGCTATTGTGTG[C/T]TCTGGTATGTGAGCG | 321006 |
rs30121819 | snp | C/T | 0.5 | 0 | intron-variant | Vprbp | GRCm38.p3 | 9:106840409 | GTCCGTCTGTTCTGT[C/T]TGTCTGTCTCTGGGT | 321006 |