SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3706601 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Rnf165 | Mm_Celera | 18:77469963 | GAAAAACACAGTGGT[A/G]TCTGCTAAGAAATTA | 225743 |
rs3708864 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Rnf165 | Mm_Celera | 18:77470268 | TAGTCTCTTGGTGAG[A/G]TTATCTGTATACACA | 225743 |
rs6300830 | snp | A/G | 0.5 | 0 | intron-variant | Rnf165 | Mm_Celera | 18:77485307 | CCTGCTAGATCATGC[A/G]GCATCTGAGGGGTCC | 225743 |
rs6301326 | snp | C/T | 0.5 | 0 | intron-variant | Rnf165 | Mm_Celera | 18:77485369 | CAGAAAGATCCCCAC[C/T]GATGTAAGAGTGAGG | 225743 |
rs6301899 | snp | C/T | 0.5 | 0 | intron-variant | Rnf165 | Mm_Celera | 18:77485467 | AATTTGGAGAGCAGA[C/T]GGGGAGTTGAGCAAA | 225743 |
rs6301956 | snp | C/T | 0.5 | 0 | intron-variant | Rnf165 | Mm_Celera | 18:77485499 | ATGAGAAATCAGAAA[C/T]GCAGCACCTACCAAA | 225743 |
rs6328476 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Rnf165 | Mm_Celera | 18:77498987 | CTGCTCCGGCACAAT[C/T]GGGTGATCTGGCTTC | 225743 |
rs6329622 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Rnf165 | Mm_Celera | 18:77499179 | CCAGTTATAGCACAG[C/T]GAGTGCATNCAATGG | 225743 |
rs6329636 | snp | A/C | 0.5 | 0 | intron-variant | Rnf165 | Mm_Celera | 18:77499188 | GCACAGNGAGTGCAT[A/C]CAATGGACCCAGCCG | 225743 |
rs6378043 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Rnf165 | Mm_Celera | 18:77469129 | AATGAACCCAAGCTT[A/G]GAGCAAGAGGACCCT | 225743 |
rs6378058 | snp | A/G | 0.5 | 0 | intron-variant | Rnf165 | Mm_Celera | 18:77469140 | GCTTNGAGCAAGAGG[A/G]CCCTCAGGNAGCTCC | 225743 |
rs6378078 | snp | G/T | 0.5 | 0 | intron-variant | Rnf165 | Mm_Celera | 18:77469149 | AAGAGGNCCCTCAGG[G/T]AGCTCCAGATCATTG | 225743 |
rs6378572 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Rnf165 | Mm_Celera | 18:77469207 | GGAGAGAAGGAGAGA[A/G]CGCCAGTAAGGGGaa | 225743 |
rs6379612 | snp | A/G | 0.5 | 0 | intron-variant | Rnf165 | Mm_Celera | 18:77469393 | AAATCAAGCCAGGTA[A/G]AAACTTAGATCCCGA | 225743 |
rs6380147 | snp | A/G | 0.5 | 0 | intron-variant | Rnf165 | Mm_Celera | 18:77469473 | AGGTCTGTGGAGAAA[A/G]NGCACACAGAGAAAC | 225743 |
rs6380159 | snp | C/T | 0.5 | 0 | intron-variant | Rnf165 | Mm_Celera | 18:77469474 | GGTCTGTGGAGAAAN[C/T]GCACACAGAGAAACC | 225743 |
rs6380247 | snp | C/T | 0.5 | 0 | intron-variant | Rnf165 | Mm_Celera | 18:77469529 | CAGGCACACTGCTAA[C/T]GNGCACCAGGGTCAT | 225743 |
rs6380249 | snp | A/T | 0.5 | 0 | intron-variant | Rnf165 | Mm_Celera | 18:77469531 | GGCACACTGCTAANG[A/T]GCACCAGGGTCATGG | 225743 |
rs6380797 | snp | C/T | 0.5 | 0 | intron-variant | Rnf165 | Mm_Celera | 18:77469627 | actacaaaaagatat[C/T]gaagctcacgaaata | 225743 |
rs6396610 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Rnf165 | Mm_Celera | 18:77542257 | GAAAGGGCTTTTGCA[C/T]GGTGCTGTCTTGTAC | 225743 |
rs6396710 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf165 | Mm_Celera | 18:77542323 | AGGGAGGAGTGAGTC[A/G]GAAAACTGGGATCGC | 225743 |
rs6397150 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77542372 | GAAAAGACACAATCC[A/C]CTTGGGTTTCAAGAA | 225743 |
rs29537105 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77535053 | CTTTAAGACACTGTC[C/T]GACATGGCCCATCCA | 225743 |
rs29547476 | snp | A/C | 0.32 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77496171 | CACAACGTCTAGTTC[A/C]GCCCCAGCAGCTGGG | 225743 |
rs29548496 | snp | G/T | 0.32 | 0.24 | utr-variant-3-prime | Rnf165 | GRCm38.p3 | 18:77460270 | AGACGGGGCCTGGGA[G/T]GAGGCAGGCAGCCAT | 225743 |
rs29550690 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77532697 | TCTATGAGGGACCTG[A/G]AGTGGGTGAACCCAT | 225743 |
rs29551090 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77502620 | GCCCCTAGGAAATCT[A/G]TCTTTCCTCTTTCCA | 225743 |
rs29553740 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77490315 | GCTTGTTGACCCAGG[A/T]CACTCCCCATCAGCC | 225743 |
rs29553771 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77532973 | CCGTGGTGGGGGGGG[C/T]TCTTGTGTGTGAGAA | 225743 |
rs29554637 | snp | A/C | 0.375 | 0.216506 | utr-variant-3-prime | Rnf165 | GRCm38.p3 | 18:77457241 | ATCCGCTCCTTCTCT[A/C]GGACTGACCACCTAA | 225743 |
rs29556293 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77489747 | CACCCACCTACATTC[A/T]TATCGCCATGGCTTC | 225743 |
rs29557948 | snp | C/T | 0.444444 | 0.157135 | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77513617 | CCTGGGGAGAGGATA[C/T]GCTGATGAAATAGTT | 225743 |
rs29558240 | snp | C/T | 0.455 | 0.143091 | intron-variant | Rnf165 | Mm_Celera | 18:77472168 | AAACACCGATTTTTA[C/T]CTGGAAAACAACAGT | 225743 |
rs29559863 | snp | A/C | 0.197531 | 0.244432 | intron-variant | Rnf165 | Mm_Celera | 18:77540598 | TCTAGAATGGAATCC[A/C]AGGGTTTGGTGGAGC | 225743 |
rs29560177 | snp | C/T | 0.375 | 0.216506 | utr-variant-3-prime | Rnf165 | Mm_Celera | 18:77460857 | GGGGGGGCATGGGGA[C/T]ACACGGTTCTTTCTC | 225743 |
rs29562235 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77516743 | TGAGGAAAAGGAGGA[C/T]GCTATATGAGTTTCC | 225743 |
rs29568913 | snp | C/G/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | GRCm38.p3 | 18:77556716 | CTCAAAAATTTAAGG[C/G/T]GGGTGTGGGGCTGGG | 225743 |
rs29568929 | snp | C/G | 0.5 | 0 | intron-variant | Rnf165 | Mm_Celera | 18:77501592 | GGAGGAGTCAGAGAC[C/G]AACCTGCTCAAAGGC | 225743 |
rs29571122 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77505713 | TAAAACAGGGAAACC[C/G]GGCTCCTCAAAAAGA | 225743 |
rs29576765 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Rnf165 | Mm_Celera | 18:77555001 | CCTCTTGACCTGCTT[C/T]GACTTCCTCCTCTGC | 225743 |
rs29577492 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77466433 | CAGCCAATATCTGCA[C/T]ATTCAACCTTCGTTC | 225743 |
rs29578426 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77537674 | GACCATAGGTATTTA[A/G]GGTGGAGGAAGAAAA | 225743 |
rs29580946 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Rnf165 | Mm_Celera | 18:77502403 | TCGACCGTAGCCATC[A/G]GGCCTCACTGCGGGC | 225743 |
rs29581735 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77501596 | GAGTCAGAGACCAAC[C/T]TGCTCAAAGGCTTCC | 225743 |
rs29581778 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf165 | GRCm38.p3 | 18:77477136 | AATAAAAATAAATTC[C/T]GTCACAGAGCAACCA | 225743 |
rs29581812 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Rnf165 | Mm_Celera | 18:77530091 | TCTGTCCCTTAAACT[C/G]TATGTATTGACACTT | 225743 |
rs29582560 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77467900 | CTCTGGTCTTACAAG[A/C]ATGCACCACCATGCC | 225743 |
rs29588753 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77470454 | GTCCTTCACTGTAAG[C/G]CACTGAAAAACCGGA | 225743 |
rs29618479 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Rnf165 | Mm_Celera | 18:77470649 | TCAGAAGTCTCACTG[C/T]AGGGGAGCCGAGGTC | 225743 |
rs29621774 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Rnf165 | Mm_Celera | 18:77529291 | GCTTTGAACACCAAG[C/T]CCACAAATTTGTTTC | 225743 |
rs29621871 | snp | C/T | 0.5 | 0 | intron-variant | Rnf165 | Mm_Celera | 18:77536937 | TTGGCACTCAAAACA[C/T]GTGTTCAAACATTCC | 225743 |
rs29623894 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77556693 | GGTCTAGACAACTTA[C/T]GGAGACTCTCAAAAA | 225743 |
rs29624597 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime | Rnf165 | Mm_Celera | 18:77462069 | TCCCGCCCCTGCTCT[A/G]GGCACGGCCAGCTCC | 225743 |
rs29624973 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Rnf165, LOC105246499 | Mm_Celera | 18:77516334 | GAAGAAAGTAAGATC[A/G]TTGACTGGATCCAGA | 225743 |
rs29626630 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77506407 | GGTCCCCTCATCTGT[A/G]CACAGGGCATAGTGA | 225743 |
rs29626863 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77467839 | TGAGAAGGCAAGGCT[A/G]GCTAACCAGTGAGCC | 225743 |
rs29629455 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77490464 | AGAAAGGCCCAGCCT[C/T]GCTCGATCGCTCGCT | 225743 |
rs29630222 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77465676 | GTGCAGGAATAGAAA[C/G]CCTGACTAAGACTTT | 225743 |
rs29630904 | snp | C/T | 0.375 | 0.216506 | utr-variant-3-prime | Rnf165 | Mm_Celera | 18:77460630 | CACAACTAAGAGCTA[C/T]ACTCGAGTTAGAATT | 225743 |
rs29633419 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77532393 | CTGCGATCTGGCTGG[A/G]GCCTGAGACTGGAAA | 225743 |
rs29640325 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77471375 | TCATGATGAAAAGGA[C/T]GACAATATCTCCTTC | 225743 |
rs29670224 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77480509 | TTTGAGACATTGAAG[A/T]AGGAAACTGAAGAAG | 225743 |
rs29671923 | snp | C/G | 0.304688 | 0.243945 | intron-variant | Rnf165 | Mm_Celera | 18:77535772 | GTTGACTAGAAACTC[C/G]CTAGGTCCATTCCTG | 225743 |
rs29672104 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77501820 | ATACTGAAGGGTGGG[A/T]GGGAGAGCTATCTGG | 225743 |
rs29672890 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77482868 | CATCAGAGAGGCATC[A/C]CCCCTGCAGCAGATT | 225743 |
rs29672895 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77471596 | TGGAAACCTCACTGG[A/G]CTGGGTGGGTCAATA | 225743 |
rs29673171 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77504576 | AGCTACCCTGTGCCA[C/T]CCAACACCAGGACAG | 225743 |
rs29675936 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77470525 | CATACAGAGTTGTGA[C/T]CCAGGTGACCCTACA | 225743 |
rs29676038 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77495525 | TTAACTGGACCTTGT[C/T]GCCTCTGCTAACCTC | 225743 |
rs29676176 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77504470 | CCTTCAAGCAGAGAG[A/G]GCGAGATTCTGAAGG | 225743 |
rs29676999 | snp | A/G | 0.444444 | 0.157135 | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77513756 | ACCTTAATCAGCCAT[A/G]ACTGTTGGAGGTAGA | 225743 |
rs29677581 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77532032 | ATGGGGTCTGAAATT[C/T]CATATGCAATCTGGA | 225743 |
rs29678355 | snp | C/T | 0.5 | 0 | intron-variant | Rnf165 | Mm_Celera | 18:77483106 | TGAACCCAGAGACAC[C/T]GAGGCAGCATGCACG | 225743 |
rs29686108 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Rnf165 | Mm_Celera | 18:77466405 | ACATGCACAAATACA[C/T]TCATGAGCACTCCAG | 225743 |
rs29686109 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77535275 | GAAATACATGTTCTG[C/T]AACCTTGCTAAAATG | 225743 |
rs29688884 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77466420 | TTCATGAGCACTCCA[A/G]CCAATATCTGCATAT | 225743 |
rs29720834 | snp | C/G | 0.375 | 0.216506 | utr-variant-3-prime | Rnf165 | GRCm38.p3 | 18:77460834 | TCTAGGTGATGTGGG[C/G]CGGGGGGGGGGGGGG | 225743 |
rs29721705 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77528908 | TCTGTCAAAAGCGTG[A/G]TGGCACACATCTTTA | 225743 |
rs29722584 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77466913 | TAAAGGAATGAAGTC[A/G]GTGCCCTTCAGGGCA | 225743 |
rs29723806 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77504273 | CACAGGAAGGCATAA[C/T]CCCAGTCGACTGACA | 225743 |
rs29723824 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77517446 | GGGCCTGTCCTTTCC[A/G]AGGTCCCAGGCTAGG | 225743 |
rs29724341 | snp | A/G | 0.48 | 0.0979796 | upstream-variant-2KB, utr-variant-5-prime | Rnf165 | Mm_Celera | 18:77566114 | ACTTCCGCGTTCACA[A/G]GCAAATAGGTGACTT | 225743 |
rs29724343 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Rnf165 | Mm_Celera | 18:77502175 | ACACACCATCCTCTC[C/T]ATGCATCAGAACCTG | 225743 |
rs29725651 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77479835 | GATGCAGGGATGGTT[C/T]AACGTATATAGATAA | 225743 |
rs29725744 | snp | C/T | 0.188366 | 0.242283 | intron-variant | Rnf165 | Mm_Celera | 18:77503312 | CCTCCAGAGTGGAAA[C/T]GGGGTCCTGGTTATC | 225743 |
rs29728062 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77530761 | TCTGACTTGTCCCCA[A/G]CACCACCCTTCAGTC | 225743 |
rs29728390 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77472547 | ATTTTCAGTTTTTTT[A/T]AAAAAAGGGTAAAAA | 225743 |
rs29728818 | snp | A/C/G | 0.375 | 0.216506 | intron-variant | Rnf165 | GRCm38.p3 | 18:77529243 | TCCACCCAGCTACTC[A/C/G]GTTATATTCCTCACT | 225743 |
rs29767311 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77491046 | TGCCACCTTCCCTCA[C/T]AGACTGTCACTCCTG | 225743 |
rs29769580 | snp | A/C/G | 0.244898 | 0.249948 | intron-variant | Rnf165 | GRCm38.p3 | 18:77503019 | AAGACAGCCACCAGA[A/C/G]TGTGGTTATCTGTCA | 225743 |
rs29769634 | snp | C/T | 0.375 | 0.216506 | utr-variant-3-prime | Rnf165 | Mm_Celera | 18:77460814 | TGGAGGGTGTTAACT[C/T]TCAGATCTAGGTGAT | 225743 |
rs29771585 | snp | A/G/T | 0.32 | 0.24 | intron-variant | Rnf165 | GRCm38.p3 | 18:77486917 | ATAAACAGGGGCCAG[A/G/T]AATTTTAAAATCAAC | 225743 |
rs29771616 | snp | C/T | 0.5 | 0 | intron-variant | Rnf165 | Mm_Celera | 18:77498355 | TGCAGATCCCTGTGT[C/T]TTCTGTGGAACATGA | 225743 |
rs29771651 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77534919 | TGGGAAGAAGGCCCA[A/G]GTGCCTCCAAGCAGG | 225743 |
rs29772741 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77532754 | GAGGGGACATGGGCA[A/G]TTAAAGTGTAATAAC | 225743 |
rs29773048 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Rnf165 | Mm_Celera | 18:77540769 | AAAACTGGCTTTCCC[A/G]AGAATTCATCCCAAG | 225743 |
rs29773363 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77521993 | CCAGGCATGGTGTCA[C/T]ATACCTTTAATCCCA | 225743 |
rs29774096 | snp | A/G | 0.32 | 0.24 | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77509064 | AAGACCTGAAAGCCA[A/G]GTGGATCCAGCTTGA | 225743 |
rs29776321 | snp | C/G | 0.375 | 0.216506 | upstream-variant-2KB | Rnf165 | Mm_Celera | 18:77567036 | GACGTTAGCCAACAC[C/G]GAACTACTAGAATCT | 225743 |
rs29781412 | snp | A/G | 0.498615 | 0.0262793 | utr-variant-3-prime | Rnf165 | Mm_Celera | 18:77460159 | ACTCCTCAGAGTTCC[A/G]CCAGGCCGAGACATC | 225743 |
rs29811254 | snp | A/C/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | GRCm38.p3 | 18:77470785 | GAGCAGTGTTTCTCA[A/C/T]GTTGTGGGTCCTGAC | 225743 |
rs29816096 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Rnf165 | Mm_Celera | 18:77539109 | GGATATGAAGAGGAT[A/G]GAGATACATAGGAAA | 225743 |
rs29819999 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77518703 | AGACAGACAGACAGA[C/G]AGAGAACTAGCCTGT | 225743 |
rs29821469 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77506579 | TGTCCTCAGCGTCAA[C/T]GGCAGTGAGGAGCCA | 225743 |
rs29821808 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Rnf165 | Mm_Celera | 18:77556905 | CACGCCGAGGCATTC[C/T]ATGCATGCGCTCAGC | 225743 |
rs29825401 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77553512 | CGGAAGGGGAGGGAA[C/T]ACCTGGGTGGGGTTC | 225743 |
rs29827150 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77489926 | CTTCGCTGAACTGTG[A/G]GTGAGGGTGGTGCGG | 225743 |
rs29832314 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77469558 | ATGGCAGAAGGAATC[C/G]TCCGGAAGCGGCTCC | 225743 |
rs29834379 | snp | A/G/T | 0.375 | 0.216506 | intron-variant | Rnf165 | GRCm38.p3 | 18:77525531 | CCTGGATCTGGGACC[A/G/T]CTCTTGTAGCTTCAA | 225743 |
rs29858911 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77501720 | GACACACACACACAC[A/C]CCAACAGGCCCCAGA | 225743 |
rs29865105 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Rnf165, LOC105246499 | Mm_Celera | 18:77515880 | ATTCAGTCCCTATCC[A/G]CTTTCTATGTTGCTG | 225743 |
rs29865599 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77496311 | AACGGGAAGGAGCAC[A/G]GCTGCATGCCTACTA | 225743 |
rs29867326 | snp | A/G/T | 0.244898 | 0.249948 | intron-variant | Rnf165 | GRCm38.p3 | 18:77502520 | AACCTCCTCTCTACC[A/G/T]CGTGGGCGGAAACCA | 225743 |
rs29868632 | snp | C/G | 0.652778 | 0.158966 | intron-variant | Rnf165 | GRCm38.p3 | 18:77465514 | CAGTAAGCAGCACCC[C/G]CACATCAGCTCTCTG | 225743 |
rs29875074 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Rnf165 | Mm_Celera | 18:77521201 | TTCGGTGGGAAACTG[A/G]CACTTGAAGGCCACG | 225743 |
rs29877867 | snp | C/T | 0.5 | 0 | intron-variant | Rnf165 | Mm_Celera | 18:77463370 | GGGCGTGGTGGTGCA[C/T]GCCTTTAATCCCTGC | 225743 |
rs29879045 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf165 | Mm_Celera | 18:77534655 | AGCTGAGGGAAGCTG[A/G]GTGTCTTTCATGTCA | 225743 |
rs29879643 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77554650 | ACCCCTGCTGTGGAG[A/G]CCCTGGGGAGCATAA | 225743 |
rs29879742 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77523578 | ATTTGAGGGGTCCCT[A/G]GAGACCACTTCAGAA | 225743 |
rs29880942 | snp | C/G | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77493006 | CCCTTTCCCTGGGAT[C/G]ATACAGTTTAGAATC | 225743 |
rs29883855 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77530820 | TATGTCTCTATGTCT[A/G]TCTATCTGTCTGTAT | 225743 |
rs29905558 | snp | A/C | 0.32 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77521188 | TTTTCACCTTTGCTT[A/C]GGTGGGAAACTGACA | 225743 |
rs29907224 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Rnf165 | Mm_Celera | 18:77529591 | GTATCACTGTCTAAA[C/T]GTGCCATGCAGTGAT | 225743 |
rs29911708 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77560899 | GGAGGGGTCACAGGG[C/G]TTTCTGTCCCAAGCC | 225743 |
rs29911967 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77471210 | GAGATCTGCTGCAAC[A/G]AGACTTAACAAGCCT | 225743 |
rs29914222 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Rnf165, LOC105246499 | Mm_Celera | 18:77515879 | AATTCAGTCCCTATC[C/T]ACTTTCTATGTTGCT | 225743 |
rs29915015 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77527698 | ACTAGCTAGGACCAG[A/T]GTGTCCCAGCAGCAC | 225743 |
rs29916194 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77527888 | TGGGTAGGCTAGATG[C/T]TCCAACAGGAAAGAC | 225743 |
rs29923264 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB, missense | Rnf165 | Mm_Celera | 18:77565828 | GAACAAATGCCTTGT[C/T]AAAGCAGGACGTTTG | 225743 |
rs29925192 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Rnf165, LOC105246499 | Mm_Celera | 18:77515884 | AGTCCCTATCCACTT[C/T]CTATGTTGCTGAAGA | 225743 |
rs29929817 | snp | G/T | 0.32 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77535842 | CTTGTCCCAAATTTC[G/T]ACTAGTCCCCAGAGC | 225743 |
rs29930686 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77472374 | TGTTGTTGTTGTTTA[A/G]CCTAGCTATGAGGGC | 225743 |
rs29935632 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Rnf165 | Mm_Celera | 18:77535517 | GAGCTGTATGCCCGC[A/C]TCATCATCCAAACCT | 225743 |
rs29955486 | snp | A/G | 0.188366 | 0.242283 | intron-variant | Rnf165 | Mm_Celera | 18:77466254 | CTAGCTCGGTCCCAC[A/G]CAGTTCAGAGGCCTT | 225743 |
rs29962560 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Rnf165 | Mm_Celera | 18:77462497 | GCAGCAGGAGCAGGG[A/G]CTAAGGACCACTGGA | 225743 |
rs29964340 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77477254 | AAGGCACAGAGAATA[C/G]TTTCAACAAAATCAT | 225743 |
rs29967814 | snp | C/T | 0.5 | 0 | intron-variant | Rnf165 | Mm_Celera | 18:77520033 | CCATAAACTGAAAGT[C/T]GGTAAACACAAAGGT | 225743 |
rs29969495 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77557219 | GAACATACACCCACC[C/T]CCTCATAGCTTCACA | 225743 |
rs29970748 | snp | G/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Rnf165, LOC105246499 | Mm_Celera | 18:77515678 | CAACTCAGGACCCTG[G/T]TTTTAGCCTGTTTAA | 225743 |
rs29974499 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77493024 | ACAGTTTAGAATCCT[A/G]TTTCCTATTTTCTCA | 225743 |
rs29980607 | snp | C/G | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77489734 | TAAACGACGTGACCA[C/G]CCACCTACATTCATA | 225743 |
rs30003603 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77489763 | TATCGCCATGGCTTC[A/C]CCTCTGTGTTCAATG | 225743 |
rs30008624 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77535840 | CTCTTGTCCCAAATT[C/T]CGACTAGTCCCCAGA | 225743 |
rs30012770 | snp | A/C/T | 0.375 | 0.216506 | intron-variant | Rnf165 | GRCm38.p3 | 18:77493897 | TGGCAACAGACACTA[A/C/T]TGCGCTAAACCCTCA | 225743 |
rs30017583 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Rnf165 | Mm_Celera | 18:77471082 | TCTATGTTTGAGAAC[A/G]AGACTTCTAGTTGAT | 225743 |
rs30018650 | snp | A/C | 0.32 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77530830 | TGTCTATCTATCTGT[A/C]TGTATGTCTCTGTAT | 225743 |
rs30024883 | snp | A/C | 0.32 | 0.24 | intron-variant | Rnf165 | GRCm38.p3 | 18:77479891 | AAAGGAAAAACAAAA[A/C]AAAACAAAACAAAAC | 225743 |
rs30024948 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77554835 | CCAAGCTGAGGTTCC[C/T]TCCCTCACTCCAGCC | 225743 |
rs30025842 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77493016 | GGGATCATACAGTTT[A/G]GAATCCTATTTCCTA | 225743 |
rs30029614 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77558052 | TCCCAGACATCACCA[C/T]AGTCCTCTTCTCTCT | 225743 |
rs30060894 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77538464 | AGCCTCCCCCAGCCT[G/T]AAGCGGGCTGGTACA | 225743 |
rs30060915 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77470477 | AAACCGGACAGAATA[C/T]ATATGATATCTGCTC | 225743 |
rs30060976 | snp | A/G | 0.375 | 0.216506 | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77511061 | TGACTTAGCCAGCAA[A/G]CTCAGGCCATACCAC | 225743 |
rs30064225 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77528951 | GGGAGGCAGAGGCAG[G/T]CAGATTTCTGAGTTC | 225743 |
rs30064585 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77486610 | TGTTCCCACGCACAC[C/T]GCTGCTCAGGACTCC | 225743 |
rs30066197 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77467780 | CTCAGGAGCCGCCCT[C/T]CTTATTCTGTGAGAC | 225743 |
rs30069343 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77534602 | GTAATGAGGGCTTGA[G/T]TCTATGAATACTGGA | 225743 |
rs30069467 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77501518 | AAGGTGGCTGCTCTC[A/T]GCTCTGACCTTTGAG | 225743 |
rs30079793 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Rnf165 | Mm_Celera | 18:77535348 | CATGCTGGCTTTCTC[A/G]TCTGTACCACTGGGA | 225743 |
rs30080547 | snp | A/G | 0.375 | 0.216506 | utr-variant-3-prime | Rnf165 | GRCm38.p3 | 18:77457242 | TCCGCTCCTTCTCTA[A/G]GACTGACCACCTAAC | 225743 |
rs30103139 | snp | C/G | 0.197531 | 0.244432 | intron-variant | Rnf165 | Mm_Celera | 18:77474710 | TCATTCTCACCTGTC[C/G]TGGAAGAGCCTCCAA | 225743 |
rs30110837 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77524359 | CCAGCCATTTGTGTC[C/T]CAGCCATCCAGGGAC | 225743 |
rs30111101 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77506406 | AGGTCCCCTCATCTG[C/T]GCACAGGGCATAGTG | 225743 |
rs30115485 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Rnf165 | Mm_Celera | 18:77470976 | CGGAGAATGGCTGGC[A/G]CATCCTGACATTCCA | 225743 |
rs30117696 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77470876 | ATTTACATTACAGAT[A/C]ATAACAGCAGAATTA | 225743 |
rs30118394 | snp | A/G | 0.188366 | 0.242283 | intron-variant | Rnf165 | Mm_Celera | 18:77538405 | GAGTGTTGCTTAGGA[A/G]GTGACATCTAGGGAC | 225743 |
rs30119178 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77480186 | GAAGGAGATCAAAGG[G/T]ATACAAACAGGAAAG | 225743 |
rs30120085 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77466527 | GAGAAAATCCTGAGG[C/T]GCCTGCTCTGCTGTA | 225743 |
rs30130248 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Rnf165 | Mm_Celera | 18:77500995 | GACTAACAAGAAGAA[C/T]CCTGGTCACCGGTCA | 225743 |
rs30131179 | snp | C/G | 0.32 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77470535 | TGTGACCCAGGTGAC[C/G]CTACAACTCACTGCC | 225743 |
rs30149709 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77517969 | CAGGAGTAGAAGCTG[G/T]CGGCGGGGTGGGGGG | 225743 |
rs30150508 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77483128 | GCATGCACGGGGCCC[A/G]AGCAGATCTGCACCA | 225743 |
rs30156606 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77506238 | AGTGCCTGGCTTGTT[G/T]CGGCTGGTACTGTGT | 225743 |
rs30160878 | snp | A/G | 0.265928 | 0.249492 | utr-variant-3-prime | Rnf165 | Mm_Celera | 18:77458011 | GTTCTGAAACCTTCT[A/G]AGTGGGATCCCAAGT | 225743 |
rs30161722 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77529432 | GGGCGTCATCTCAGC[C/T]ACACCAACACTCAGT | 225743 |
rs30162708 | snp | A/G | 0.375 | 0.216506 | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77508862 | TGAGATGGATGGATC[A/G]GAAAATCGAAGAGGG | 225743 |
rs30163303 | snp | A/T | 0.32 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77496137 | CATGGCAACGCCAGA[A/T]GAGGTAGCAAGACGA | 225743 |
rs30166773 | snp | G/T | 0.197531 | 0.244432 | intron-variant | Rnf165 | Mm_Celera | 18:77547590 | ATGATTGTTTGAAGA[G/T]TCTATAGATCTGTGG | 225743 |
rs30167182 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77495428 | CATTTTTGGCCCTCT[C/T]ATGTGACACCGTCAG | 225743 |
rs30172981 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Rnf165, LOC105246499 | Mm_Celera | 18:77515593 | AGGGCTACAGACCCC[A/G]GAGGAGGGCTGTGTT | 225743 |
rs30173086 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77466865 | CTTTGCGCAGGAAGC[C/T]GGCTCACTGCCCCAG | 225743 |
rs30203749 | snp | C/G | 0.375 | 0.216506 | utr-variant-3-prime | Rnf165 | GRCm38.p3 | 18:77460840 | GATGTGGGGCGGGGG[C/G]GGGGGGGGCATGGGG | 225743 |
rs30212142 | snp | A/C | 0.375 | 0.216506 | utr-variant-3-prime | Rnf165 | Mm_Celera | 18:77460782 | CTCCCCTGAGAGAAC[A/C]GAAAGCACATCAGGG | 225743 |
rs30213967 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77472278 | GCACTCAGGAGGCCA[A/G]AGGAAGGCTAATCAC | 225743 |
rs30217260 | snp | C/G | 0.32 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77476834 | TAAAGTCACCTGTAC[C/G]AATATGGCAGAACTC | 225743 |
rs30217791 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77511340 | CCCATGTGCACATTC[C/T]CACCTCACTATGATC | 225743 |
rs30222142 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77506584 | TCAGCGTCAACGGCA[G/T]TGAGGAGCCAGGCTA | 225743 |
rs30222591 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77535453 | ATTTCAGCTCTCAGT[C/T]CCCACATAAGCAAAC | 225743 |
rs30223548 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77547205 | ACGGGAAAGGGATTG[A/G]TAGCCAGTTTATGGG | 225743 |
rs30246882 | snp | C/T | 0.444444 | 0.157135 | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77514410 | CCTTGTTAGAGCGGG[C/T]GTGGCCTTGTTTGAG | 225743 |
rs30250311 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77465718 | ACTTGTTTTTCTCTG[A/G]GATTTTGTCACAGCG | 225743 |
rs30252085 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77504507 | TTACTGTGAATGCAC[A/C]ATTTTCTAAATAGGG | 225743 |
rs30253147 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | Rnf165 | Mm_Celera | 18:77459662 | AAATTTAGGGAGCAT[C/T]CAATCAACTTCCCTG | 225743 |
rs30257834 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Rnf165 | Mm_Celera | 18:77474340 | TCCTCTGTCACCTGT[A/G]CAATCCACATACATT | 225743 |
rs30259002 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77521571 | TGAAGCAGGCATAGA[A/G]TTTCAGGTCCAGGAT | 225743 |
rs30259816 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77535756 | TGCTGCTGTCTCTCC[C/T]GTTGACTAGAAACTC | 225743 |
rs30261320 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77492834 | GCCCCAACTGAGATG[A/G]CCTTGGCGCTGAGGG | 225743 |
rs30262628 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77486048 | TCTGTAATGGGATCC[A/G]ATGCCCTCTTCTGGT | 225743 |
rs30264459 | snp | A/G | 0.5 | 0 | intron-variant | Rnf165 | Mm_Celera | 18:77564232 | TGATTTCCGAAGCGC[A/G]TAAGCACCTGCTCAC | 225743 |
rs30269579 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77535196 | AGATGTGACCCACTC[A/G]CCTCTGAAATACATG | 225743 |
rs30270221 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77518216 | GCATTCACAGCACAA[A/G]AGAGTGAGTCTCCTA | 225743 |
rs30278787 | snp | A/C | 0.32 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77536230 | GGACAAGATAATGAA[A/C]CATCCTTCAGTCTTC | 225743 |
rs30278916 | snp | C/G | 0.32 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77532551 | CCTCTGCTTTGTATG[C/G]CCTATTTTGGAACCT | 225743 |
rs36246933 | snp | A/G | 0.260355 | 0.249785 | downstream-variant-500B | Rnf165 | Mm_Celera | 18:77455868 | AGGTTACCACATGGT[A/G]GCTTGCGAGTAAAGA | 225743 |
rs36252576 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Rnf165 | Mm_Celera | 18:77545371 | GCCACACCTCACACC[A/G]GGCTGGGTACTTGAT | 225743 |
rs36258594 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Rnf165 | Mm_Celera | 18:77555350 | GAGGTTTTGTGGAAG[A/G]GCCTCTTTTGGCTGA | 225743 |
rs36261916 | snp | C/G | 0.473373 | 0.11227 | intron-variant | Rnf165 | Mm_Celera | 18:77500689 | GGGTTGGTCGAGGAT[C/G]CAGGGATTTGATTTC | 225743 |
rs36262114 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77500056 | TTTTTAATTGCCCTG[A/T]CCGGTTCTTCAAAAC | 225743 |
rs36271583 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Rnf165 | Mm_Celera | 18:77542335 | GTCAGAAAACTGGGA[C/T]CGCCATGGAACGGTC | 225743 |
rs36280936 | snp | A/T | 0.18 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77529666 | TTAGTGAGCCCTATC[A/T]ATCCCACAATGTTCC | 225743 |
rs36305119 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rnf165 | Mm_Celera | 18:77490361 | GAGTGAGCAGTGGAG[C/T]GTAGCCCATGGAAGA | 225743 |
rs36307580 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Rnf165 | Mm_Celera | 18:77466504 | GACTGCATCTGATGT[A/G]GGCCAATGAGAAAAT | 225743 |
rs36312515 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Rnf165 | Mm_Celera | 18:77555740 | ACCTCATCTCTGATA[C/G]TTGCTCTCCTGGGCT | 225743 |
rs36313369 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Rnf165 | GRCm38.p3 | 18:77468514 | AGTACCACCCTGTCG[A/G]GTTTCAGAAGAGGGA | 225743 |
rs36314345 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Rnf165 | Mm_Celera | 18:77501410 | CCGGTGAAAGAGTGG[C/T]CACCAGACAGCACAT | 225743 |
rs36316458 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rnf165 | Mm_Celera | 18:77546189 | GTATAGAAAGCTAAA[C/T]ATACTGCCCTCCAAA | 225743 |
rs36320411 | snp | G/T | 0.32 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77539052 | AACATCAAGTTCACA[G/T]AAAGACAAAATTTTG | 225743 |
rs36322794 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Rnf165 | Mm_Celera | 18:77525015 | AGCCTATTTACACCG[C/G]TCTCCCTTTCACAGG | 225743 |
rs36325439 | snp | C/T | 0.375 | 0.216506 | intron-variant, downstream-variant-500B | Rnf165, LOC105246499 | Mm_Celera | 18:77507655 | CAGGCCTCTGGATCC[C/T]GTTAGCATTTTGCTT | 225743 |
rs36326039 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77553609 | AATCGGCTTCTGCCA[C/T]CGTCTTGTGGCACTA | 225743 |
rs36328386 | snp | A/G | 0.391111 | 0.206368 | utr-variant-3-prime | Rnf165 | GRCm38.p3 | 18:77456606 | TTGTGCTCCACCGGC[A/G]TGGTGGGTGACTCCA | 225743 |
rs36333862 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Rnf165 | GRCm38.p3 | 18:77457310 | TAGCTAGTCTTTGCA[C/T]CTGCAGGATGTTGTA | 225743 |
rs36333987 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rnf165 | Mm_Celera | 18:77548467 | CTGGTCACACCAGCT[A/C]CTCCACCCTTCAGCA | 225743 |
rs36347584 | snp | A/C | 0.5 | 0 | intron-variant | Rnf165 | Mm_Celera | 18:77487899 | AATTGACTGAGACAG[A/C]GCGGAGTAAGGAGAC | 225743 |
rs36348806 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Rnf165 | Mm_Celera | 18:77545353 | AGCTCTGCTAAACTT[C/T]GTGCCACACCTCACA | 225743 |
rs36350047 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77504757 | AGCTCCAAGTGTGGA[A/G]TGTTTGCAGTCATCC | 225743 |
rs36352083 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Rnf165 | Mm_Celera | 18:77503258 | ACTCATCATTTCCCA[C/T]ACTGAGCTTTGTCCC | 225743 |
rs36357914 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf165 | Mm_Celera | 18:77545322 | TCATGTGCTCACAGT[C/T]ACTTCCATGGGACTA | 225743 |
rs36365572 | snp | C/T | 0.391111 | 0.206368 | downstream-variant-500B | Rnf165 | Mm_Celera | 18:77456035 | GGGGAAATACATTGG[C/T]CAACTGAGGTTCTTT | 225743 |
rs36386461 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Rnf165 | Mm_Celera | 18:77548859 | CAGTCTACAAACCCT[A/G]GGAGCTATGTTCTGG | 225743 |
rs36404378 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Rnf165 | Mm_Celera | 18:77556846 | TGCACAACAAATGCA[A/T]ATACAGAAATGCGGG | 225743 |
rs36407264 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Rnf165 | Mm_Celera | 18:77556820 | GTTTATATGTCAACT[C/T]TACACACAAGTGCAC | 225743 |
rs36415925 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77537271 | TTAAAACATATGTTC[C/T]GGCTTTCCACAGACT | 225743 |
rs36436210 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Rnf165 | Mm_Celera | 18:77546782 | TGAAACTCTGCCAAG[A/G]AAGAACCAGACTAGA | 225743 |
rs36436406 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B | Rnf165 | Mm_Celera | 18:77455781 | ACGTCTTGGTCCACA[A/G]TTGTCAACCTGTTGC | 225743 |
rs36457789 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Rnf165 | Mm_Celera | 18:77503567 | TCTTGTGCGGGTTTC[A/G]GTTTATACGTCCATG | 225743 |
rs36465506 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77533258 | CCAGTTCTGCTCCCT[C/T]GGGCATCCAGTTACT | 225743 |
rs36467760 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Rnf165 | Mm_Celera | 18:77544871 | CATCAACAGACTGAG[A/G]GCCACTGAAGGAGTC | 225743 |
rs36507039 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77501211 | CACAGAAGGTGATCA[C/T]TCAGGGTCAGCTGTG | 225743 |
rs36510997 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Rnf165 | Mm_Celera | 18:77552676 | TAGCAGGAGAGACAC[A/G]TGTAACCTCGAGGGC | 225743 |
rs36528958 | snp | C/G | 0.21875 | 0.248039 | intron-variant | Rnf165 | Mm_Celera | 18:77533285 | TACTCTGAGCTCAGC[C/G]AGCCTGTGTGTGGTG | 225743 |
rs36535992 | snp | G/T | 0.408163 | 0.193609 | synonymous-codon | Rnf165 | GRCm38.p3 | 18:77462990 | TGTCCTGGGGTCTTC[G/T]CTGTGAATAGAGAAA | 225743 |
rs36545558 | snp | A/G | 0.5 | 0 | intron-variant | Rnf165 | Mm_Celera | 18:77494296 | GGTGTTATGAGCCTG[A/G]TGCACTGAGGGCCTG | 225743 |
rs36556207 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rnf165 | Mm_Celera | 18:77546625 | TTCATAAGGCAACAT[A/C]TTTTTCAGCTTCTGC | 225743 |
rs36565957 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Rnf165 | Mm_Celera | 18:77549286 | AAAACAGTTGACGTG[A/G]CAGGCCTCACGCCTT | 225743 |
rs36566960 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Rnf165 | Mm_Celera | 18:77545183 | CCCTCTGAAGTTCCT[A/G]CACAATCACAAGGAA | 225743 |
rs36570189 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77499922 | AAACTGAAGCGTGTA[C/T]GTAGTAGATTCCATG | 225743 |
rs36586192 | snp | C/T | 0.18 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77536543 | GCCCAATCCAGAATG[C/T]GAGTGTGCACTTGCC | 225743 |
rs36591724 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Rnf165 | Mm_Celera | 18:77537585 | ATAAGAAATCTGGGG[A/G]AACTCACGGGCACAT | 225743 |
rs36594088 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77475601 | TGCACAGAAAGCAAG[A/G]ATGGCCAGTGTGTTA | 225743 |
rs36594737 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Rnf165 | Mm_Celera | 18:77553463 | GCCGTGTCCTTGAGA[C/T]GATTTCTAACACGGG | 225743 |
rs36597506 | snp | C/G | 0.336735 | 0.234472 | utr-variant-3-prime | Rnf165 | Mm_Celera | 18:77457898 | CTCAGGGGGTCCAGG[C/G]ACTGACTTACCCTTG | 225743 |
rs36599130 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Rnf165 | GRCm38.p3 | 18:77461472 | AGAAACCCAGTGAGA[C/T]CCAGTCTGCTCCTTT | 225743 |
rs36619993 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Rnf165 | Mm_Celera | 18:77531239 | GAGCAGTGTCCTTCA[C/T]ACCCTGCCACTACAG | 225743 |
rs36633608 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf165 | Mm_Celera | 18:77555088 | TCTGATGAACACTGA[C/T]GAGAGCAGAACGGAA | 225743 |
rs36639420 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf165 | Mm_Celera | 18:77546354 | CTGCATATCAAAGAC[A/G]GCAAGTGCCTCTCTC | 225743 |
rs36641591 | snp | C/G | 0.459184 | 0.136902 | intron-variant | Rnf165 | Mm_Celera | 18:77500770 | CCACCCACCCCATGG[C/G]AGTTTGAGTTCAGAC | 225743 |
rs36662116 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77546766 | CAGGACTAAGGGCCA[A/T]TGAAACTCTGCCAAG | 225743 |
rs36662236 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf165 | Mm_Celera | 18:77470566 | TTGCCTGAGAAGGTA[C/T]ATCTGAACCAGAGAT | 225743 |
rs36663214 | snp | C/T | 0.408163 | 0.193609 | utr-variant-3-prime | Rnf165 | GRCm38.p3 | 18:77459243 | GCTGAGGCCTGGACC[C/T]GCCTCATCGCCGCTC | 225743 |
rs36679154 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Rnf165 | Mm_Celera | 18:77537375 | ACCAACCTCACAGTC[A/G]GCCGTGATACACACA | 225743 |
rs36681988 | snp | G/T | 0.165289 | 0.235211 | intron-variant | Rnf165 | Mm_Celera | 18:77529604 | AATGTGCCATGCAGT[G/T]ATGGGTTCATACCAC | 225743 |
rs36695644 | snp | A/G/T | 0.142012 | 0.225474 | intron-variant | Rnf165 | GRCm38.p3 | 18:77552007 | CCATCACTGCTCTCC[A/G/T]GGAGACCATGGAACC | 225743 |
rs36704036 | snp | C/G | 0.32 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77533981 | CACATATATACATTT[C/G]TCTCTGGGTCTGGGT | 225743 |
rs36706191 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Rnf165 | Mm_Celera | 18:77537474 | TATTGCCTTAGAATA[A/G]AGTTCATGTGGCGTC | 225743 |
rs36709172 | snp | A/C | 0.444444 | 0.157135 | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77509928 | TATGATCAGAGGTCG[A/C]AAAGAGGGAAAAGAA | 225743 |
rs36712956 | snp | A/C | 0.35503 | 0.226867 | intron-variant | Rnf165 | Mm_Celera | 18:77537619 | TTCAACTGTATCTTA[A/C]AACCAGTCCCTGACC | 225743 |
rs36713062 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77501855 | AGAAGGGGCTGTGCT[C/T]TGATTCCCTAGGCTG | 225743 |
rs36718868 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf165 | Mm_Celera | 18:77547303 | AGTCTTCTCAACAGC[A/G]AGTGTCTTCTGAGAT | 225743 |
rs36723217 | snp | A/G | 0.18 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77530308 | AAATCCATAGTCAGG[A/G]CATGTTGCCTTGGGG | 225743 |
rs36743390 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77545764 | GGCTGGACTCAAAGA[A/G]GTTTCATGAGGTCCG | 225743 |
rs36744423 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Rnf165 | Mm_Celera | 18:77531514 | AGCATGTTGGCCTAC[A/G]GGTAAGGTGCCCAGC | 225743 |
rs36752413 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Rnf165 | Mm_Celera | 18:77549949 | CCTTACTGGAAGCAG[A/G]CGTGTAGGAGCCTTC | 225743 |
rs36759608 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf165 | Mm_Celera | 18:77558869 | AGCATTGCTCGTTGA[A/G]TCTCAGCCTTAGGAG | 225743 |
rs36768196 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77491758 | TAAATGAGGTCAAGA[C/T]GGTAAGGCCTTCACT | 225743 |
rs36786527 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf165 | Mm_Celera | 18:77553449 | ATCCCTTTGCACTTG[C/T]CGTGTCCTTGAGACG | 225743 |
rs36786766 | snp | G/T | 0.473373 | 0.11227 | intron-variant | Rnf165 | Mm_Celera | 18:77552815 | CTGAAAAGGTTGACC[G/T]CGTTAGAGGAAGACT | 225743 |
rs36787947 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Rnf165 | Mm_Celera | 18:77536755 | AGAAAAGCTGAACCA[A/G]AGCTCAGTGAGGCTG | 225743 |
rs36789355 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Rnf165 | Mm_Celera | 18:77557926 | GAAAACCTAGCAGCC[A/G]GATCTACCTGAGAAC | 225743 |
rs36797460 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77546361 | TCAAAGACGGCAAGT[A/G]CCTCTCTCCACCGCC | 225743 |
rs36804153 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rnf165 | Mm_Celera | 18:77545281 | ATAGTTACCACAGTA[C/T]GTTCACATGAGCATG | 225743 |
rs36809586 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf165 | Mm_Celera | 18:77545107 | CCTCAGGTTTCAAGC[C/T]TATTGCCTTTGAGTG | 225743 |
rs36811897 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77503545 | CTACCTAAAACGGAA[A/G]CCTCACTCTTGTGCG | 225743 |
rs36826208 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf165 | Mm_Celera | 18:77475748 | CAGGTAGGCAGAAAC[C/T]GTGTCCCTGAGTCTG | 225743 |
rs36827071 | snp | G/T | 0.18 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77531905 | AGCTGCCATTAACTC[G/T]AAGCTGTTTGGGGTA | 225743 |
rs36830953 | snp | C/T | 0.18 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77544328 | GTTCTGTGGCTTCAT[C/T]GTCCTTGCCTTACAG | 225743 |
rs36840493 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Rnf165 | Mm_Celera | 18:77544489 | AGAACTATGGAGGGT[C/T]CCCTTCCTGGAACCT | 225743 |
rs36843796 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77526496 | CTGGATGTTAGAGAA[A/G]CCAGAAGTCACAGTT | 225743 |
rs36852038 | snp | A/C | 0.132653 | 0.220748 | utr-variant-3-prime | Rnf165 | Mm_Celera | 18:77458034 | TCCCAAGTATAGCTT[A/C]GTAACTGTCCTCGGG | 225743 |
rs36854776 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Rnf165 | Mm_Celera | 18:77542340 | AAAACTGGGATCGCC[A/G]TGGAACGGTCTTTGA | 225743 |
rs36871393 | snp | G/T | 0.35503 | 0.226867 | utr-variant-3-prime | Rnf165 | GRCm38.p3 | 18:77459211 | TGTCTCTCTCCTGGA[G/T]ATGGTGGATGTGAGA | 225743 |
rs36874991 | snp | C/T | 0.391111 | 0.206368 | utr-variant-3-prime | Rnf165 | GRCm38.p3 | 18:77460746 | GACTTTCCGTCTCCT[C/T]TCTCACTAAACCCTC | 225743 |
rs36876534 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Rnf165 | GRCm38.p3 | 18:77492303 | AGTGACAGCTTCTCT[A/G]GACAGACAAGTTGTA | 225743 |
rs36882157 | snp | A/G | 0.197531 | 0.244432 | downstream-variant-500B | Rnf165 | Mm_Celera | 18:77455994 | AGGAAGCGCCTAGCC[A/G]GGGACCAAGCAACCT | 225743 |
rs36892272 | snp | C/G | 0.165289 | 0.235211 | intron-variant | Rnf165 | Mm_Celera | 18:77529871 | TCTGTCTATTACCTC[C/G]TAGCAAAGGTCTCTA | 225743 |
rs36910948 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Rnf165 | Mm_Celera | 18:77556045 | ACATCAAGAGGAAAT[C/T]GGGGCTTTTTTAGAA | 225743 |
rs36918373 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf165 | Mm_Celera | 18:77558825 | TCAGGCCCTCTGCTC[A/G]GATGTCTCAGGAAGT | 225743 |
rs36921098 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf165 | Mm_Celera | 18:77542038 | GCGCTGCAATCCAGG[A/G]TGTCCCCAGGAATGG | 225743 |
rs36929382 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77502082 | GGTGCGCAGTGTTCC[C/T]GTGAGCTTCCAAGGG | 225743 |
rs36935777 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Rnf165 | Mm_Celera | 18:77544347 | CTTGCCTTACAGTTC[A/G]TGGGCTGCTCTGAGG | 225743 |
rs36970665 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77464084 | CCTGGCTAGAGCACA[C/T]GAGGAAACCTATGTT | 225743 |
rs36971398 | snp | A/C | 0.32 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77505833 | AGCTGGTGGCAATAA[A/C]TAATCCCAGGGCTTC | 225743 |
rs36972878 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Rnf165 | Mm_Celera | 18:77457345 | GAGGACTCTGTGGGC[C/T]GCTGCTATGAGCAGA | 225743 |
rs37011661 | snp | C/G | 0.244898 | 0.249948 | downstream-variant-500B | Rnf165 | Mm_Celera | 18:77455875 | CACATGGTAGCTTGC[C/G]AGTAAAGAGGAGGTT | 225743 |
rs37016887 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77502310 | ACAGAATGCCTCTAA[A/G]GTCCAGTGGCCTTCA | 225743 |
rs37023946 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Rnf165 | Mm_Celera | 18:77533611 | CTGGGACTCAGAAAG[A/G]CTGGAGAGAGCTCAC | 225743 |
rs37025005 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Rnf165 | Mm_Celera | 18:77488439 | CCATTAGAGTCATTC[C/T]GTCCCATTAAAAAAT | 225743 |
rs37025681 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Rnf165 | Mm_Celera | 18:77540664 | GTACCCTGCAACCCA[C/G]TCCTTTATGTTAAGC | 225743 |
rs37027700 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Rnf165 | Mm_Celera | 18:77470185 | CCACTTTTGAGGACT[A/G]CCTCAGTGATGTCAT | 225743 |
rs37052415 | snp | A/G | 0.18 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77536312 | GATGTGGAGCACACT[A/G]AGCAAGTCAAGGCTG | 225743 |
rs37054525 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77503705 | ACTCAGCTAAGAACC[A/G]GGGCCTGCTAGCAAC | 225743 |
rs37059421 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Rnf165 | Mm_Celera | 18:77555099 | CTGACGAGAGCAGAA[A/C]GGAAGCCCTATCCAG | 225743 |
rs37064684 | snp | A/C | 0.197531 | 0.244432 | intron-variant | Rnf165 | Mm_Celera | 18:77533190 | TTCTGGGAAAGCCGG[A/C]AGCTGCCAGGAGGGC | 225743 |
rs37065950 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Rnf165 | Mm_Celera | 18:77557538 | ATAATAGGCTGACCC[C/T]GAGATCAACGCTTTC | 225743 |
rs37078209 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77499987 | TGGGTGTCTGAACAC[G/T]TATGTATGCTTTTTC | 225743 |
rs37081785 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77503122 | TCCAGAAGGCTCTCC[C/T]GCGCACTCTGGCTCA | 225743 |
rs37085933 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Rnf165 | Mm_Celera | 18:77549097 | ACACAACCCTAAGAA[A/G]CAGGAGTGCTGGTCG | 225743 |
rs37088851 | snp | C/G | 0.375 | 0.216506 | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77513102 | TTATCGGATAGCATT[C/G]TCATGGCAATAGCTA | 225743 |
rs37098030 | snp | C/T | 0.336735 | 0.234472 | utr-variant-3-prime | Rnf165 | GRCm38.p3 | 18:77456489 | CGGGGCATTGCCAGC[C/T]GGAGCATAGGGCCTG | 225743 |
rs37099781 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Rnf165 | Mm_Celera | 18:77500026 | GCTTTTCTACTGTGT[A/G]CATATGTGATTTGGT | 225743 |
rs37101584 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Rnf165 | Mm_Celera | 18:77463744 | TCACATGGTACGTGT[A/G]CCCACGTGGAAGGCA | 225743 |
rs37101809 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Rnf165 | Mm_Celera | 18:77474184 | GATCCTCATTCTTCA[C/T]GTTCCTTGGGGCAAC | 225743 |
rs37111894 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Rnf165 | Mm_Celera | 18:77549399 | TCCCATTATTCTTCA[A/G]ATGAGAAAACTAAGG | 225743 |
rs37127192 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77503736 | TTGGAGTGACATCAC[C/T]GTCAGGTGTCAGGAG | 225743 |
rs37135429 | snp | C/T | 0.5 | 0 | intron-variant | Rnf165 | Mm_Celera | 18:77475770 | CTGAGTCTGTTCATG[C/T]TCTACCATCATGCTC | 225743 |
rs37144001 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77531967 | TCTCAATAGACCTTC[A/T]GCCTTGTGTGCTACT | 225743 |
rs37161920 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rnf165 | Mm_Celera | 18:77544029 | AACAACTTCTCAGCT[A/C]ATCCAGCAGTCCAGG | 225743 |
rs37178889 | snp | A/T | 0.444444 | 0.157135 | downstream-variant-500B | Rnf165 | Mm_Celera | 18:77455642 | ACTGATCCTTGGCTA[A/T]AGGAATGAGTCTATT | 225743 |
rs37179362 | snp | A/T | 0.18 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77543781 | AAGTAGGGTGGTTGA[A/T]GGAGTATTTCAATTT | 225743 |
rs37188924 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77542094 | CACCTATAAACTAAG[C/T]CCTGTGGCTCTTCCT | 225743 |
rs37199819 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Rnf165 | GRCm38.p3 | 18:77556906 | ACGCCGAGGCATTCC[A/G]TGCATGCGCTCAGCG | 225743 |
rs37201609 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Rnf165 | Mm_Celera | 18:77495395 | ACAGGTCCTGGAGGC[C/T]ACTCTTGCAGCCTGG | 225743 |
rs37204103 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Rnf165 | Mm_Celera | 18:77468792 | GCCAGGAAAAGCACA[A/G]AGGCATCCAGGCAAC | 225743 |
rs37206682 | snp | A/G | 0.391111 | 0.206368 | utr-variant-3-prime | Rnf165 | GRCm38.p3 | 18:77456406 | CAGCCCCCTCGGAGG[A/G]CCTGGTGCAGCCCTC | 225743 |
rs37213996 | snp | A/C | 0.32 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77535552 | TTTCGTTTTGTTTGC[A/C]CATCTAATTCTCTCA | 225743 |
rs37219843 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77539711 | GAGTCAGTAATAGAA[A/G]AAGCAGGTTTGAGCT | 225743 |
rs37236152 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Rnf165 | Mm_Celera | 18:77537385 | CAGTCAGCCGTGATA[C/T]ACACACTGCTACCTA | 225743 |
rs37237833 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Rnf165 | Mm_Celera | 18:77537026 | ATACTGGGCCTGCTA[C/T]GAGCTCTCATGTACA | 225743 |
rs37246002 | snp | G/T | 0.297521 | 0.245442 | intron-variant | Rnf165 | Mm_Celera | 18:77539021 | GGAAACACTGAAAAT[G/T]GACTAAAGGAAAGGG | 225743 |
rs37257636 | snp | A/G | 0.391111 | 0.206368 | utr-variant-3-prime | Rnf165 | GRCm38.p3 | 18:77459255 | ACCTGCCTCATCGCC[A/G]CTCCTTCCTGGCTTC | 225743 |
rs37264423 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77546608 | GAATGAATGTGTGGA[C/T]GTTCATAAGGCAACA | 225743 |
rs37267619 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rnf165 | Mm_Celera | 18:77548069 | CCCGTGTGTTGCAGG[C/T]TCAGTTCTAGATGGT | 225743 |
rs37269770 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77546882 | ATCACTGTCATCTTA[C/T]GGTGCTCGTCCATTC | 225743 |
rs37275851 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Rnf165 | Mm_Celera | 18:77475231 | GATAGTGCCCAGCTC[C/T]ACTGAGTGAATTCCT | 225743 |
rs37282476 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Rnf165 | Mm_Celera | 18:77555707 | CTGCTCCCTATAGGC[C/T]GAGGCTCCTGGCTCT | 225743 |
rs37310751 | snp | A/T | 0.459184 | 0.136902 | intron-variant | Rnf165 | Mm_Celera | 18:77538925 | ACATCCCAGTAGGAA[A/T]CAAGTGAAAGTATCT | 225743 |
rs37328776 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77539690 | TCTGGTCTACCCAAC[A/G]CCTGGGAGTCAGTAA | 225743 |
rs37332108 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Rnf165 | Mm_Celera | 18:77494181 | GGAGCCATCAGTCAG[C/T]GTGTGTCACCATCAA | 225743 |
rs37347158 | snp | A/T | 0.426035 | 0.177515 | intron-variant | Rnf165 | Mm_Celera | 18:77552127 | AGCGGGCAATACTTT[A/T]GTTCCGTTGATGGTT | 225743 |
rs37369792 | snp | C/T | 0.32 | 0.24 | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77513568 | CAGGTGACTGGATTC[C/T]CTCACACAGATGCCC | 225743 |
rs37374691 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77545456 | CTGACAAAAGCCCAG[A/T]CTGCTGTCGGACCCT | 225743 |
rs37406769 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf165 | Mm_Celera | 18:77544552 | CCTGTCCTCATACAC[C/T]GCCTCACACCAAGTC | 225743 |
rs37409477 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77541528 | CAGTCCAATCTTAGT[A/T]CGCACATACAGAACA | 225743 |
rs37410166 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Rnf165 | Mm_Celera | 18:77551867 | TGCCACCCACGTTCC[C/T]GTGCCAAGTTCAATC | 225743 |
rs37414520 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77487129 | ACACACACCTCATAT[A/G]GACTTTTGTAATGGA | 225743 |
rs37422397 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Rnf165 | Mm_Celera | 18:77553221 | ACCCCACGTTGCTAC[C/T]CAGACTGACCACTGA | 225743 |
rs37429369 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Rnf165 | Mm_Celera | 18:77545340 | TTCCATGGGACTAAG[A/C]TCTGCTAAACTTTGT | 225743 |
rs37434331 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Rnf165 | Mm_Celera | 18:77548828 | TTCCCTTTTCATAAG[A/G]TAAGTGTGCCCTCTC | 225743 |
rs37442407 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77503502 | TTGCTGGCCCTGGGC[A/C]TGGGCAACTGTGGAA | 225743 |
rs37489960 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Rnf165 | Mm_Celera | 18:77547072 | GGGACAGCAGAGACC[C/T]AAAGGACACTCCAAG | 225743 |
rs37498531 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77505203 | AAATTCCTTCCATGC[A/G]GCAGGCAGTTACTTG | 225743 |
rs37505506 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Rnf165 | Mm_Celera | 18:77469933 | ACAGGCAACCACACA[C/G]TGTACTTTCTGGTAG | 225743 |
rs37512039 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77500870 | AAGTCGGAGCTCAGC[A/G]TCTTGAGTCAGTCTG | 225743 |
rs37527361 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Rnf165 | Mm_Celera | 18:77475006 | TCACGCTCTCTGCAC[C/T]GCCTTTCTTATACGC | 225743 |
rs37564087 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Rnf165 | Mm_Celera | 18:77548198 | GGAGAATGTCTGTGG[A/G]TGGTTTTGCCTAGGT | 225743 |
rs37583163 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77548258 | GTGAGACATGCCCTT[C/T]CACCAGGATGTCTTC | 225743 |
rs37589027 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf165 | Mm_Celera | 18:77465075 | ATCCACGGATGCATT[C/T]CTAATTTGACAGCAT | 225743 |
rs37592933 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Rnf165 | Mm_Celera | 18:77471809 | CTCCCACAGAAGGAA[C/T]AGCAATGAATGTAAA | 225743 |
rs37608513 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf165 | Mm_Celera | 18:77548103 | TAGGTGGTTCTTAGA[C/T]GGTGAGAGTATTAAC | 225743 |
rs37613411 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Rnf165 | Mm_Celera | 18:77533641 | CTACATTCTGAACTT[A/G]CTAGCGCAGTCCCCC | 225743 |
rs37622369 | snp | C/G/T | 0.124444 | 0.216185 | utr-variant-3-prime | Rnf165 | GRCm38.p3 | 18:77460477 | ACGGGTTGAGGTTTC[C/G/T]GAGAGCAGTGCAAAT | 225743 |
rs37659037 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Rnf165 | Mm_Celera | 18:77501418 | AGAGTGGCCACCAGA[C/T]AGCACATTGAGCTTC | 225743 |
rs37659230 | snp | C/T | 0.444444 | 0.157135 | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77508214 | GTGGCCATGCAACTG[C/T]GCAACCTGGAGCATC | 225743 |
rs37661950 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Rnf165 | Mm_Celera | 18:77550944 | AGTTCTGTGCCTGGC[C/T]TGACGTGTTAGCATG | 225743 |
rs37678476 | snp | A/C | 0.444444 | 0.157135 | utr-variant-3-prime | Rnf165 | GRCm38.p3 | 18:77461006 | CTCGAAACAATGGCT[A/C]TCTCTGAGGGTCTAA | 225743 |
rs37683145 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Rnf165 | Mm_Celera | 18:77499611 | AACTGCTCTATGGCC[A/G]CACAATATAGAGCCT | 225743 |
rs37712319 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Rnf165 | Mm_Celera | 18:77554512 | GACTCAGAGTTCTGG[A/G]ACCTTCCAAGTACAT | 225743 |
rs37730493 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Rnf165 | Mm_Celera | 18:77544302 | CTGAAGGATGAGCTG[C/T]AGCCTCCTAAGTTCT | 225743 |
rs37742047 | snp | A/G | 0.408163 | 0.193609 | downstream-variant-500B | Rnf165 | Mm_Celera | 18:77455986 | GCCTTCTCAGGAAGC[A/G]CCTAGCCGGGGACCA | 225743 |
rs37764681 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Rnf165 | Mm_Celera | 18:77542978 | AATCTAACACCAGGA[A/G]CCTTTGGGGCCATGG | 225743 |
rs37840945 | snp | A/G | 0.497778 | 0.0332592 | utr-variant-3-prime | Rnf165 | Mm_Celera | 18:77461140 | TGCCGATGCTGTGCC[A/G]TCTGATTCATCTGGT | 225743 |
rs37886127 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Rnf165 | Mm_Celera | 18:77555135 | CTGTGATCACCCTCT[A/G]CAGAAGCTGGGTACA | 225743 |
rs37904833 | snp | G/T | 0.408163 | 0.193609 | utr-variant-3-prime | Rnf165 | GRCm38.p3 | 18:77458025 | TGAGTGGGATCCCAA[G/T]TATAGCTTAGTAACT | 225743 |
rs37905203 | snp | A/C | 0.46875 | 0.121031 | intron-variant | Rnf165 | Mm_Celera | 18:77487379 | ATATTGATGAGACTA[A/C]AGCTAACTCTACCAT | 225743 |
rs37925726 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Rnf165 | Mm_Celera | 18:77541921 | CTGTTCATTTAAGGG[A/G]CAAGTGCAGGCTTAC | 225743 |
rs37927216 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf165 | Mm_Celera | 18:77549873 | ACTAATCCTGGGCTA[C/T]GCATGTCAAGTCCAT | 225743 |
rs37933921 | snp | C/G | 0.21875 | 0.248039 | intron-variant | Rnf165 | GRCm38.p3 | 18:77475117 | GCTGTACTCTAGAGT[C/G]CCCTGGTTTATAGTA | 225743 |
rs37938546 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Rnf165 | Mm_Celera | 18:77544420 | ATCCCTAGCTCTACT[C/G]TTCATTTATTCAGGC | 225743 |
rs37939691 | snp | A/G | 0.459184 | 0.136902 | utr-variant-3-prime | Rnf165 | GRCm38.p3 | 18:77460106 | GGCCACACTCAGCAC[A/G]CCTGACCTTCACCAT | 225743 |
rs37946274 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77545735 | CCTCTTAGCCATCTG[G/T]AGCCAGTGTCTTGGG | 225743 |
rs37983467 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Rnf165 | Mm_Celera | 18:77555811 | CCATCATGTGGGTGA[C/T]GTCACCATTCATCCC | 225743 |
rs38023247 | snp | A/G | 0.391111 | 0.206368 | utr-variant-3-prime | Rnf165 | Mm_Celera | 18:77459959 | TTGGACACAGCCATC[A/G]GAGGAGCAGCAGGAA | 225743 |
rs38026304 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Rnf165 | Mm_Celera | 18:77529581 | ACCAACATCTGTATC[A/G]CTGTCTAAATGTGCC | 225743 |
rs38035357 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77537646 | GACCTGGGAAATGTG[G/T]TTGCCATTCAGTGAC | 225743 |
rs38043539 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77549145 | GTGTACTGGGCTGCC[A/G]TTCTTGCTCTCTGAC | 225743 |
rs38084770 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Rnf165 | Mm_Celera | 18:77474648 | CTCTTTCTGGCACCC[A/G]GAGAGGAGCACGGGA | 225743 |
rs38117271 | snp | C/T | 0.124444 | 0.216185 | missense | Rnf165 | Mm_Celera | 18:77475579 | GACACTCGATCCTGA[C/T]TCCGCCTGCACAGAA | 225743 |
rs38118823 | snp | A/C | 0.444444 | 0.157135 | utr-variant-3-prime | Rnf165 | GRCm38.p3 | 18:77462173 | CTCCCTCAGACACCG[A/C]TACCAACTCCTCTTT | 225743 |
rs38139287 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77504726 | ATCAGACTGGGAATG[G/T]AAATTGTGGATTCCC | 225743 |
rs38155479 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77500683 | AATGCTGGGTTGGTC[A/G]AGGATCCAGGGATTT | 225743 |
rs38165651 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77556907 | CGCCGAGGCATTCCA[C/T]GCATGCGCTCAGCGG | 225743 |
rs38173330 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Rnf165 | Mm_Celera | 18:77558303 | TCCTGTGCAAACTTG[A/T]CTACATATTCTATAG | 225743 |
rs38203920 | snp | A/G | 0.18 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77530530 | CGGGCATGATCTAGC[A/G]TCATCCCACAAATGG | 225743 |
rs38210426 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77545747 | CTGGAGCCAGTGTCT[C/T]GGGCTGGACTCAAAG | 225743 |
rs38238317 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Rnf165 | Mm_Celera | 18:77468142 | AGAACTGGGGCTGAG[A/G]ATGGGCGGCAGCAGC | 225743 |
rs38247602 | snp | A/G | 0.18 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77533489 | TTTTCCTCTTGCCAC[A/G]TCACTTTCAATGGGG | 225743 |
rs38249478 | snp | A/C | 0.18 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77529454 | ACACTCAGTTGTCAG[A/C]ACACCCACTTCAGTC | 225743 |
rs38282271 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Rnf165 | Mm_Celera | 18:77546271 | TGTTGATGACCATAG[A/G]GATCCCATGTGCACT | 225743 |
rs38358835 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Rnf165 | Mm_Celera | 18:77538955 | TTTTCCCAAGAAGCC[C/T]CAGGAAGAGGTGACA | 225743 |
rs38364470 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Rnf165 | Mm_Celera | 18:77556878 | GGCGTTCCACGCATG[C/T]GCCCAGCGGATCACG | 225743 |
rs38365219 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Rnf165 | Mm_Celera | 18:77530348 | AACAGCCAGCAGAAT[C/T]TTCCTGAATCAAGGA | 225743 |
rs38383811 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77503036 | GTGGTTATCTGTCAA[A/G]ACACTCGCCCAATAC | 225743 |
rs38386408 | snp | C/T | 0.32 | 0.24 | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77508342 | TGCCATGTGTCCCAA[C/T]GGTATCTGGTGTCTC | 225743 |
rs38390135 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Rnf165 | Mm_Celera | 18:77546338 | AGGCATAAGGCCAGC[A/C]CTGCATATCAAAGAC | 225743 |
rs38410414 | snp | A/G | 0.32 | 0.24 | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77510744 | AACACCCAGGTTTGC[A/G]CTCTACCAGATGCTT | 225743 |
rs38417651 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Rnf165 | Mm_Celera | 18:77552441 | ACACGGATATCCATC[A/G]CTGTTCTTATGTGGG | 225743 |
rs38448935 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rnf165 | Mm_Celera | 18:77496728 | AAGTATTGATGATGG[C/T]CATGAAAACACAGAA | 225743 |
rs38450284 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rnf165 | Mm_Celera | 18:77506722 | AGCTGATTAGGACCT[A/G]TAGCATGTGCCACGT | 225743 |
rs38498823 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | GRCm38.p3 | 18:77543701 | CAAGATCCTTGCCAC[G/T]GCTGGAGTCCACAGT | 225743 |
rs38501719 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77543694 | ACTCGCCCAAGATCC[G/T]TGCCACGGCTGGAGT | 225743 |
rs38543478 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Rnf165 | Mm_Celera | 18:77547141 | GAAGGGACAGCACAC[C/T]TTTAGGTCTTTTGTA | 225743 |
rs38602624 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Rnf165 | Mm_Celera | 18:77552132 | GCAATACTTTTGTTC[C/T]GTTGATGGTTTAGGG | 225743 |
rs38607580 | snp | A/G | 0.32 | 0.24 | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77508037 | AGCTATCATTTGGGA[A/G]CAAAGTCCTACCAAA | 225743 |
rs38670488 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Rnf165 | Mm_Celera | 18:77554467 | CTGCAATTTGTTCTC[A/G]CCTTAAGTCCAGGTC | 225743 |
rs38681607 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Rnf165 | Mm_Celera | 18:77551548 | GCATCAAGTTTAATG[A/G]ACATTTCTGGAAGCC | 225743 |
rs38700120 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Rnf165 | Mm_Celera | 18:77556300 | CCATCTGATGGACAC[A/G]GTACCAGAAACGATG | 225743 |
rs38722586 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf165 | Mm_Celera | 18:77543376 | AAGGTGCCATGTTCC[C/T]AGGAAGATTTCTTCA | 225743 |
rs38753657 | snp | A/C/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Rnf165, LOC105246499 | Mm_Celera | 18:77514872 | TGGGCTGCAGTCCAG[A/C/G]GAGTCCGGGCTGATG | 225743 |
rs38777891 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Rnf165 | Mm_Celera | 18:77503743 | GACATCACTGTCAGG[A/T]GTCAGGAGCCTTGTG | 225743 |
rs38789401 | snp | C/G | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77550774 | CCTCCTCCTGGATAC[C/G]CTCTCCAGCCTGTAC | 225743 |
rs38791240 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Rnf165 | Mm_Celera | 18:77554863 | GCCGGTCTATCTTCT[C/T]GTCCACATCACAGCT | 225743 |
rs38836867 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Rnf165 | Mm_Celera | 18:77556864 | ACAGAAATGCGGGAG[A/G]CGTTCCACGCATGCG | 225743 |
rs38869822 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rnf165 | Mm_Celera | 18:77545151 | GACTGGAGGCTTAAC[A/C]GAGAGAGGATCCTGA | 225743 |
rs38907543 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf165 | Mm_Celera | 18:77554350 | AACAAGACTAGTTAT[C/T]GCAAAGTTCTAGAGT | 225743 |
rs38943293 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Rnf165 | Mm_Celera | 18:77549329 | AGAGCCTGATCCAGA[A/G]TCCAGACACTAGATG | 225743 |
rs38947386 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77546939 | TAGGTAGAAGCATCA[A/C]GCAGGCCCAGTGAGC | 225743 |
rs38950235 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Rnf165 | Mm_Celera | 18:77543903 | GTTTCTCCACGGACA[C/T]ACGAAAAAGAAAGGA | 225743 |
rs39003772 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf165 | Mm_Celera | 18:77542288 | ATGACTCCTCTCCCC[A/G]ACAAAAGGAGAAAGG | 225743 |
rs39004825 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Rnf165 | GRCm38.p3 | 18:77461118 | TTAGCCGAGGCCAAG[C/T]CTACACTGCCGATGC | 225743 |
rs39027560 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Rnf165 | Mm_Celera | 18:77542243 | ACTTCTCTAGTAAGG[A/T]AAGGGCTTTTGCACG | 225743 |
rs39051009 | snp | A/C | 0.21875 | 0.248039 | intron-variant | Rnf165 | Mm_Celera | 18:77544290 | CCAATGGGTGGCCTG[A/C]AGGATGAGCTGCAGC | 225743 |
rs39051212 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Rnf165 | Mm_Celera | 18:77528249 | CCACTGGACTGTACG[C/T]TGTTTTCCAATCTTA | 225743 |
rs39084887 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77496265 | ACTCAGAACTTGACT[C/T]ATTCATTCAGAGTAA | 225743 |
rs39104192 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Rnf165 | Mm_Celera | 18:77530039 | ACATTTTAATACTGT[C/T]TCCAATTTCTTCTCT | 225743 |
rs39187078 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77543581 | CACTACACAATGCCA[A/G]TTTCTCATAGCTGTT | 225743 |
rs39221957 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Rnf165 | Mm_Celera | 18:77551035 | AGTTATCTCAGGAAT[C/T]TGCTATGGCAGGGTG | 225743 |
rs39231561 | snp | G/T | 0.165289 | 0.235211 | intron-variant | Rnf165 | Mm_Celera | 18:77533166 | TTGTGGGAGCCTCTA[G/T]CCACCTGCTTCTGGG | 225743 |
rs39355222 | snp | A/C | 0.165289 | 0.235211 | intron-variant | Rnf165 | Mm_Celera | 18:77535358 | TTCTCATCTGTACCA[A/C]TGGGAACAAACCTCA | 225743 |
rs39368211 | snp | A/T | 0.165289 | 0.235211 | intron-variant | Rnf165 | Mm_Celera | 18:77526416 | CTCTGTACTCTTGGC[A/T]GGTGCTATACAATCA | 225743 |
rs39460592 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf165 | Mm_Celera | 18:77542470 | AGTCTACAGACATCA[A/G]AATACTGCTTTCTCT | 225743 |
rs39577507 | snp | A/C | 0.486111 | 0.0821678 | intron-variant | Rnf165 | Mm_Celera | 18:77556942 | CACCACGGTGAATGC[A/C]CCGGGTTGACTCTCT | 225743 |
rs39611611 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf165 | Mm_Celera | 18:77553318 | CCGGGGAAGTGGTGG[C/T]CAGAAGATATCTGTG | 225743 |
rs39680168 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Rnf165 | Mm_Celera | 18:77549205 | GCAGACAACGGGAGT[A/G]CGATTACAATGGCAG | 225743 |
rs39832203 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Rnf165 | Mm_Celera | 18:77544101 | CCCAGGGACTGGAAG[A/G]TGTCACAGAAGCAAA | 225743 |
rs45632523 | snp | A/G/T | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77548711 | TGGGGAGGTGTGGGA[A/G/T]TCAGGGTACCTGAGA | 225743 |
rs45653686 | snp | A/G | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77468510 | AGGGAGTACCACCCT[A/G]TCGAGTTTCAGAAGA | 225743 |
rs45655268 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77477925 | ATGGTCTCAGTTCCC[A/G]GTAAAGACACAGACC | 225743 |
rs45675021 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77485047 | GTGGATTCAACACCA[A/G]CCTAGCCTATATATC | 225743 |
rs45901046 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77465488 | AGCTGAGCAAGCCAG[A/G]GGAAGCAAGCCAGTA | 225743 |
rs45902590 | snp | A/G | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77490453 | GCGGTCAGGAAAGAA[A/G]GACCCAGCCTCGCTC | 225743 |
rs46022165 | snp | A/G/T | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77528346 | AATGTAATTGTCCTC[A/G/T]CCAAGGCTTACTGCC | 225743 |
rs46075314 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77544925 | CCTGCTGGTCCTTTG[A/G]GCCCTTGCTCCTCAA | 225743 |
rs46082271 | snp | C/T | | | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77510714 | GTGAATTCTCATCAT[C/T]GGGATCTCTAGGACA | 225743 |
rs46095026 | snp | A/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77541068 | GTGGGGAAACGGGGC[A/T]TGAAGTAGATAATAG | 225743 |
rs46160059 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77484830 | AAGGAGAAAACTGTA[C/T]ATAGAGAAAGTTTAG | 225743 |
rs46162608 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77534340 | GGGTGAGGTGGTGAC[A/G]CTTCTCTTGCCTGTG | 225743 |
rs46339589 | snp | G/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77526227 | TTGCTTCTTGGTCAT[G/T]ACGTTTGTGCAGGAA | 225743 |
rs46362286 | snp | C/T | | | intron-variant, downstream-variant-500B | Rnf165, LOC105246499 | GRCm38.p3 | 18:77507638 | GGGCCTCTCTTGGGA[C/T]GCAGGCCTCTGGATC | 225743 |
rs46433707 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77544820 | CATAGGTAGACACTG[A/G]GGCCTTGTGTGCACA | 225743 |
rs46548981 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77484773 | GCCTGACCTTCTTGA[A/G]TTGGCCTCCTTCTGA | 225743 |
rs46568675 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77484763 | CCTAAAGCCAGCCTG[A/G]CCTTCTTGAATTGGC | 225743 |
rs46687315 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77484616 | CCCCGTCTTTAATGC[C/T]CCACATAAAGGGTCT | 225743 |
rs46711810 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77546475 | CCAGTAGAGAGCAAG[C/T]TTCAAAAAGTCAGGA | 225743 |
rs46736359 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77494787 | GGTTAGGACAAGCTA[C/T]AACATCCTCCCTTTG | 225743 |
rs46744532 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77544075 | TTTCTTTTTAGCCAC[C/T]ATATTTAAAGCCCAG | 225743 |
rs46828835 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77542135 | GAAAAATCCCTGTGG[A/G]CTCAAGGGAGGCAGA | 225743 |
rs46883675 | snp | C/T | | | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77510596 | GGGGTGCCGAGTGAG[C/T]TCCAAGGAGCCTCGT | 225743 |
rs46898264 | snp | A/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77494451 | TAGGTGGGGCCTGAC[A/T]GGAGGAAGTGAGTTG | 225743 |
rs46988792 | snp | C/T | | | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77508082 | TGTGATGAGCTTAAT[C/T]TTAACATAGATTAAG | 225743 |
rs47033149 | snp | C/T | | | utr-variant-3-prime | Rnf165 | Mm_Celera | 18:77460757 | TCCTTTCTCACTAAA[C/T]CCTCAGAGACTCCCC | 225743 |
rs47068892 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77505710 | CGCTAAAACAGGGAA[A/G]CCCGGCTCCTCAAAA | 225743 |
rs47101571 | snp | A/C | | | intron-variant | Rnf165 | Mm_Celera | 18:77526529 | CACTCACAGGCGACA[A/C]TCCAATGCCCAACAA | 225743 |
rs47101913 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77484528 | CCTACCTGAGCGGGG[A/G]TCCCCACCCCTGGAC | 225743 |
rs47206614 | snp | C/T | | | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77511156 | CTCCCCCTGAGCTCC[C/T]GAGGCTGGATCTGAG | 225743 |
rs47238232 | snp | A/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77531724 | GCCTTGTTCTAAACA[A/T]TGTGAGTTCACTAAT | 225743 |
rs47244477 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77494553 | GAGCAACTTCTGTCA[C/T]GTATTCATGTGTCTA | 225743 |
rs47295067 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77540395 | CAGAGTGAGTGGGGT[C/T]GGGATACTGAGCTTC | 225743 |
rs47343548 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77533216 | AGGGCTCAGGGACAC[A/G]GGCAGGGACTGGGAG | 225743 |
rs47355351 | snp | C/T | | | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77508467 | GCTGCACCCACACCT[C/T]CCAGCTCAGTGCTGG | 225743 |
rs47356996 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77498906 | TGCTGAGGTCACTGG[A/G]GGACCATGGCCAACA | 225743 |
rs47357012 | snp | A/G | | | utr-variant-3-prime | Rnf165 | Mm_Celera | 18:77462058 | GGGCGCCCCCTTCCC[A/G]CCCCTGCTCTAGGCA | 225743 |
rs47404530 | snp | A/C | | | intron-variant | Rnf165 | Mm_Celera | 18:77484499 | AGATCTCCTGAGGAC[A/C]TGCAAAGGGCTCTCC | 225743 |
rs47426137 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77560192 | AGTAAATCAGTTCAG[C/T]TTTTCCACCCTGGCC | 225743 |
rs47489937 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77535431 | AGGGAGGGGACCCCA[A/G]ACCAGGATTTCAGCT | 225743 |
rs47503829 | snp | G/T | | | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77507805 | CCCGCGGTCACACTG[G/T]CACACTGGCACGCTC | 225743 |
rs47570725 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77504053 | CCTCTTGGGTGCTTC[C/T]TCTCCAAAAGGAAGG | 225743 |
rs47584087 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77541626 | TGTTCTTTTTTAGAA[A/G]AGCAAGAATACAGGG | 225743 |
rs47613044 | snp | A/G | | | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | GRCm38.p3 | 18:77510192 | CCCAGAGGTCCCCCC[A/G]CCCAGATCTGTTCAA | 225743 |
rs47628639 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77548719 | TGTGGGAGTCAGGGT[A/G]CCTGAGAATCCTGCT | 225743 |
rs47655608 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77543700 | CCAAGATCCTTGCCA[C/T]GGCTGGAGTCCACAG | 225743 |
rs47671927 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77504082 | GGATTGGAGGGTGAG[A/G]TGCAGGAAGCAGCAT | 225743 |
rs47716161 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77553895 | CTTGGGAACCGGTTC[C/T]CTGGGAACTGGGGTA | 225743 |
rs47772595 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77553916 | AACTGGGGTAAACTA[A/G]GGAAGCCTCAGTTTG | 225743 |
rs47780598 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77521063 | GCTTTCTTTATTTCA[A/G]TATGGCACCCGGTGA | 225743 |
rs47915389 | snp | C/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77504966 | CAGAATCAGATACTT[C/G]TGTTCATCGAGCTGA | 225743 |
rs47930267 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77493554 | CAGGGAAGGGGGGCC[A/G]TGCAGCCGGAGGGGG | 225743 |
rs47954799 | snp | G/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77475093 | AGCATCTCTGAATTC[G/T]CCTCCCAAGCTGTAC | 225743 |
rs47985747 | snp | G/T | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77528430 | TCTCGGCCTAGAATG[G/T]TTTTCAGCCTCTGAG | 225743 |
rs48032639 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77544945 | TTGCTCCTCAAAGGC[C/T]AGACAGTTTGTAGCA | 225743 |
rs48033478 | snp | A/C | | | intron-variant | Rnf165 | Mm_Celera | 18:77468834 | AGGACAGGCAGTGGA[A/C]AAACTCTCATCATTC | 225743 |
rs48049961 | snp | C/T | | | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77511005 | ACTTGAGCTGGAACC[C/T]GTCTCTGCTCCCTGT | 225743 |
rs48133998 | snp | A/G | | | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77508305 | AACCAGTGCCGTTAC[A/G]TTCTGAGAGCAGGAT | 225743 |
rs48145762 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77545217 | TGGGAAGGTCAGAAA[C/T]TTTCATCCTCACTGC | 225743 |
rs48156552 | snp | C/T | | | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77511022 | TCTCTGCTCCCTGTC[C/T]CCCCTCCCCCACTCC | 225743 |
rs48158572 | snp | C/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77546546 | ATGGGGCAGAGGCTG[C/G]AATCCATATTTGCAG | 225743 |
rs48257148 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77546261 | CAATGCTCACTGTTG[A/G]TGACCATAGGGATCC | 225743 |
rs48348348 | snp | A/G | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77475642 | GAGCCAGTCAAGCTC[A/G]CAGGAACTCTGAGTG | 225743 |
rs48365911 | snp | C/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77494845 | ATGAGGTTACTGTCC[C/G]CTCCCTGCCTGGACC | 225743 |
rs48485179 | snp | G/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77493846 | TGTGACACCAGGTCA[G/T]AACTAGGTCTGCCTT | 225743 |
rs48602793 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77542141 | TCCCTGTGGACTCAA[A/G]GGAGGCAGAAAGCAC | 225743 |
rs48627591 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77543993 | TGGGGAATATCAAGG[A/G]ACAGAGGCTCTGGGC | 225743 |
rs48650250 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77542153 | CAAGGGAGGCAGAAA[A/G]CACAAGCCTGTTGTG | 225743 |
rs48682088 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77484515 | TGCAAAGGGCTCTCC[C/T]ACCTGAGCGGGGGTC | 225743 |
rs48752873 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77528369 | TTACTGCCTCCTTCT[A/G]CTAACCTAGGCCTAG | 225743 |
rs48859350 | snp | A/C | | | intron-variant | Rnf165 | Mm_Celera | 18:77546278 | GACCATAGGGATCCC[A/C]TGTGCACTGCCTGAA | 225743 |
rs48871812 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77475794 | CATGCTCTTCTCTCC[A/G]ACACACTCTTCGTAG | 225743 |
rs48912477 | snp | G/T | | | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77511222 | AGCAGCCTCGGAGAG[G/T]CTCAGGGAACCTAAC | 225743 |
rs48933047 | snp | A/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77494586 | ACTCAATGATATTTT[A/T]AAGGAAAAAATAGAA | 225743 |
rs48946427 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77503835 | TTGGAGCAAGAACAC[C/T]AGGCTCCTGTCCTTA | 225743 |
rs48947127 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77504955 | GTCCCTTAGGGCAGA[A/G]TCAGATACTTGTGTT | 225743 |
rs49011918 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77543683 | GAAGGGATAGGACTC[A/G]CCCAAGATCCTTGCC | 225743 |
rs49086087 | snp | C/T | | | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77510585 | GGCCATTCCACGGGG[C/T]GCCGAGTGAGCTCCA | 225743 |
rs49098226 | snp | C/T | | | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77508480 | CTTCCAGCTCAGTGC[C/T]GGGAAAGAGCTTGCA | 225743 |
rs49105648 | snp | A/G | | | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77510431 | CTGCCTATGAGCACT[A/G]CCTGGGAGCACTGCC | 225743 |
rs49150478 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77551278 | GATCCTCTCCACACA[C/T]GGTATCTGTCGACAC | 225743 |
rs49175251 | snp | C/T | | | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77511086 | TACCACTGCATGTTT[C/T]GAAGAACACCGTCCA | 225743 |
rs49238926 | snp | A/C | | | intron-variant, downstream-variant-500B | Rnf165, LOC105246499 | GRCm38.p3 | 18:77507644 | CTCTTGGGATGCAGG[A/C]CTCTGGATCCCGTTA | 225743 |
rs49297674 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77493601 | GAGCGGATTTGTCCG[A/G]GGTTGAGGCAGTTAG | 225743 |
rs49356388 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77544526 | GCCCAAGCCCTCTCC[A/G]TTGAGTCTTCCCTGT | 225743 |
rs49401795 | snp | G/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77494801 | ATAACATCCTCCCTT[G/T]GGGCTCACTGCTCCC | 225743 |
rs49500404 | snp | G/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77476124 | ATACGGAAGCAGACA[G/T]GAGGGCACAGAGAAG | 225743 |
rs49513129 | snp | A/G | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77490455 | GGTCAGGAAAGAAGG[A/G]CCCAGCCTCGCTCGA | 225743 |
rs49520492 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77544697 | TTGCACATAGAATCC[A/G]CTAAGATGAGATCAT | 225743 |
rs49528394 | snp | C/T | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77468531 | TTTCAGAAGAGGGAG[C/T]ACCACCCTGTCGGGT | 225743 |
rs49550356 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77494139 | GCCCGACTCTGCACT[A/G]AGCATAGTCATGTGG | 225743 |
rs49558976 | snp | A/C | | | intron-variant | Rnf165 | Mm_Celera | 18:77533242 | GGGAGCCCATCGAGT[A/C]CCAGTTCTGCTCCCT | 225743 |
rs49668083 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77504104 | AAGCAGCATGGACCA[A/G]CCTGACTAAGCACTT | 225743 |
rs49712921 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77543972 | AAAGAGGTAGTCCTG[A/G]GTGTTTGGGGAATAT | 225743 |
rs49729840 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77533512 | CAATGGGGTATCCAT[A/G]GCCAGAGGCGCCATA | 225743 |
rs49748321 | snp | C/T | | | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77508131 | GCTTGAAGCTAAGCT[C/T]TCTACATGGTGGGTA | 225743 |
rs49750995 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77546417 | CTGTGCCATTTTGTA[C/T]GGTGGCACACATGAC | 225743 |
rs49828097 | snp | A/G | | | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77511172 | GAGGCTGGATCTGAG[A/G]CACTCCTTCTGGTCT | 225743 |
rs49830578 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77474687 | GCCAGCAAGAACTAC[A/G]CTCTGTGTCATTCTC | 225743 |
rs49832501 | snp | G/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77504068 | CTCTCCAAAAGGAAG[G/T]ATTGGAGGGTGAGGT | 225743 |
rs49841453 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77494557 | AACTTCTGTCACGTA[C/T]TCATGTGTCTACGAC | 225743 |
rs49856075 | snp | A/C | | | intron-variant | Rnf165 | Mm_Celera | 18:77534840 | TGTGGCTTTTCACAG[A/C]TCAGCAGCCAGATGC | 225743 |
rs49879819 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77524283 | CAGCGGTTCCCTTAC[C/T]TGCTACTGAGTTAAT | 225743 |
rs50020307 | snp | A/C/G | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77492678 | GTTCCTGATCACTGA[A/C/G]GATGCCACAGAGGAG | 225743 |
rs50024740 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77541909 | CCATCTATCCTGCTG[C/T]TCATTTAAGGGACAA | 225743 |
rs50092739 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77501905 | GCTGAGCTGGTGCTC[C/T]ACACTTGGGGAGAGA | 225743 |
rs50122548 | snp | G/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77504045 | TCTCTGCTCCTCTTG[G/T]GTGCTTCCTCTCCAA | 225743 |
rs50128398 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77503737 | TGGAGTGACATCACT[A/G]TCAGGTGTCAGGAGC | 225743 |
rs50142178 | snp | A/G | | | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77510271 | TCCCCAGGAAGTCAC[A/G]TGCCTTCACCCAATC | 225743 |
rs50144481 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77544073 | TATTTCTTTTTAGCC[A/G]CCATATTTAAAGCCC | 225743 |
rs50174150 | snp | A/C | | | intron-variant | Rnf165 | Mm_Celera | 18:77475643 | AGCCAGTCAAGCTCA[A/C]AGGAACTCTGAGTGA | 225743 |
rs50249456 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77494707 | GGCCCCTCCCACCAA[A/G]CCTCCCTCGGGTGCT | 225743 |
rs50371636 | snp | G/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77553909 | CTCTGGGAACTGGGG[G/T]AAACTAGGGAAGCCT | 225743 |
rs50375783 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77504731 | ACTGGGAATGTAAAT[C/T]GTGGATTCCCAGCTC | 225743 |
rs50431919 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77489199 | CAGCAATGCAAGAGG[C/T]TGTGGTCTGAACGCC | 225743 |
rs50484466 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77484722 | TTTTTTTAATAAATG[A/G]CACGTGCCAGAGGGT | 225743 |
rs50488844 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77544914 | AAGCAGCAGGACCTG[C/T]TGGTCCTTTGAGCCC | 225743 |
rs50511947 | snp | A/G | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77468544 | AGCACCACCCTGTCG[A/G]GTTTCAGAAGAGGCC | 225743 |
rs50518553 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77533119 | GGGCCGAACTTACCA[C/T]GGGAACTGCAGCACA | 225743 |
rs50552934 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77546468 | ATCTTCTCCAGTAGA[A/G]AGCAAGCTTCAAAAA | 225743 |
rs50571374 | snp | C/G | | | intron-variant, upstream-variant-2KB | Rnf165, LOC105246499 | Mm_Celera | 18:77516037 | GGGAGATGGGCCTCA[C/G]GGCATACCTAGAGGG | 225743 |
rs50603857 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77544797 | GAGTGAGAAAACACA[C/T]GCAATGACATAGGTA | 225743 |
rs50660936 | snp | A/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77494602 | AAGGAAAAAATAGAA[A/T]TCAAATCTCCAAATC | 225743 |
rs50708122 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77526367 | GGAGGGAAGGCAGGT[A/G]GCCTGCCTGTGTGGG | 225743 |
rs50762674 | snp | G/T | | | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77510324 | GTCCTGCCACACTCT[G/T]CTGGGAGGTGTTTGG | 225743 |
rs50792282 | snp | C/G | | | utr-variant-3-prime | Rnf165 | Mm_Celera | 18:77459482 | AAAAAGGAAGCAAGC[C/G]GAACCCGCCCTGCCC | 225743 |
rs50797543 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77494128 | CCGAAAGAAAGGCCC[A/G]ACTCTGCACTGAGCA | 225743 |
rs50901488 | snp | C/G | | | upstream-variant-2KB | Rnf165 | Mm_Celera | 18:77568058 | TTGGGAGGGCACAAA[C/G]TCGGAGATCAGGTTG | 225743 |
rs50936154 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77504836 | CAGGAGGCCAGGTTA[A/G]TCCAAGGCTAGCTCT | 225743 |
rs51021222 | snp | A/C | | | intron-variant | Rnf165 | Mm_Celera | 18:77474832 | CCCCCCCCCCCCAAC[A/C]CCAACTCTCTGAATG | 225743 |
rs51075350 | snp | C/T | | | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77507891 | CGGTCTCTCTGACCA[C/T]AGCCCCACCCCCCAC | 225743 |
rs51114869 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77546374 | GTGCCTCTCTCCACC[A/G]CCTCACTAATGTCAC | 225743 |
rs51115619 | snp | C/G | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77492189 | GCAGAGGCACCGACC[C/G]AGGGATGGCACGTAG | 225743 |
rs51143311 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77494224 | ACGAAGTGACAGGAG[A/G]CTCCCTGATGCCATT | 225743 |
rs51213127 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77541448 | AACTAACCTAGGGGC[A/G]GAAGGAGCGTTGTCT | 225743 |
rs51219024 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77493511 | TCAGCTTCATCCAAG[A/G]AGCTGGATTCCAGCT | 225743 |
rs51299182 | snp | A/G | | | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77508075 | AAAAAAGTGTGATGA[A/G]CTTAATTTTAACATA | 225743 |
rs51301352 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77535047 | CACTTTCTTTAAGAC[A/G]CTGTCTGACATGGCC | 225743 |
rs51310065 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77541903 | AGTGTTCCATCTATC[C/T]TGCTGTTCATTTAAG | 225743 |
rs51342307 | snp | A/C | | | intron-variant | Rnf165 | Mm_Celera | 18:77541633 | TTTTAGAAGAGCAAG[A/C]ATACAGGGATTGGAT | 225743 |
rs51382468 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77503731 | GCAACTTGGAGTGAC[A/G]TCACTGTCAGGTGTC | 225743 |
rs51384285 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77505044 | TTCCTCTCCGTCTCA[C/T]TGGATCTGTGCCACC | 225743 |
rs51505350 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77475844 | AGTTAGTCTCCTCCA[A/G]GAAGGCCTCCCTAAA | 225743 |
rs51645038 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77528075 | TCTCATAGCGTGATG[A/G]CCCCCAACCATAAAA | 225743 |
rs51679489 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77541568 | GTCTACACATACAAG[A/G]ATTTCTATGACATTT | 225743 |
rs51688880 | snp | C/T | | | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77508138 | GCTAAGCTTTCTACA[C/T]GGTGGGTACCAAGGA | 225743 |
rs51717690 | snp | A/C | | | intron-variant | Rnf165 | Mm_Celera | 18:77524282 | ACAGCGGTTCCCTTA[A/C]TTGCTACTGAGTTAA | 225743 |
rs51787958 | snp | G/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77545006 | AACAAACCAGGAAAG[G/T]CTTTAAGTCTTTACC | 225743 |
rs51851244 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77493176 | GGAGAGTTGTGAATG[A/G]CAGCCTGGGAGTCTG | 225743 |
rs51862986 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77474279 | TAAGAAAGCCAAGGG[C/T]GGGGCTGATGTGCTG | 225743 |
rs51895552 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77560903 | GGGTCACAGGGCTTT[C/T]TGTCCCAAGCCATCT | 225743 |
rs51912372 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77544913 | AAAGCAGCAGGACCT[A/G]CTGGTCCTTTGAGCC | 225743 |
rs51930728 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77541558 | ATATATGTGTGTCTA[C/T]ACATACAAGAATTTC | 225743 |
rs52015278 | snp | C/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77494662 | CAGAAACACTGCTCA[C/G]TCTACGAGGTGCCCA | 225743 |
rs52078694 | snp | A/G/T | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77503957 | CGTGCGTGCGTGTGT[A/G/T]TGTGTGTGTGTATGC | 225743 |
rs52104820 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77553711 | TAGGTGGTAGATGGT[A/G]AGCCTGAGTGTGTGT | 225743 |
rs52105677 | snp | A/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77473498 | ATAGATAATAGATAG[A/T]CAGGTGATAGATAGA | 225743 |
rs52151500 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77475354 | GAAACTCCACAGACC[C/T]GTTGCAATCTCCCCC | 225743 |
rs52166674 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77503914 | GTGCACGCGTGCACG[C/T]GCACGTGCGTGCGTG | 225743 |
rs52197010 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77534218 | ATACACACACATACA[C/T]ACACACACACACACA | 225743 |
rs52207425 | snp | C/T | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77534007 | TGGGTCTCTTTCTCT[C/T]TCTCTCTCTCTCTCT | 225743 |
rs52232304 | snp | C/G | | | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77511367 | GATCACACCTACACA[C/G]ACACACATATCCACA | 225743 |
rs52294274 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77497570 | AGATAGATAGATAGA[C/T]AGATAGACAGACAGA | 225743 |
rs52300086 | snp | A/C | | | intron-variant | Rnf165 | Mm_Celera | 18:77544130 | AATGCATGTGTATAC[A/C]TGCATGTACACACAT | 225743 |
rs52308334 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77475459 | TCCTATGCTCCCCAG[C/T]ATCTGGAGACTCACC | 225743 |
rs52339476 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77475386 | TCCTTCCCTCCCTCC[C/T]TCCCTCCCTCCTTTC | 225743 |
rs52422894 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77503911 | TGTGTGCACGCGTGC[A/G]CGCGCACGTGCGTGC | 225743 |
rs52425910 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77475382 | CCCCTCCTTCCCTCC[C/T]TCCCTCCCTCCCTCC | 225743 |
rs52483180 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77495192 | GACAGACAAAAAGAC[A/G]GAGAGGGGATGTTTG | 225743 |
rs52489793 | snp | G/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77562122 | GTTCTGTTTTGCAGG[G/T]TTTTTTTTTGTTTGT | 225743 |
rs52496153 | snp | C/T | | | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77511387 | ACATATCCACACAAA[C/T]CTATACACACACTCC | 225743 |
rs52503093 | snp | G/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77497398 | GCTAGATGGCAGATG[G/T]GTAGGTGAGTGGATG | 225743 |
rs52528316 | snp | G/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77553717 | GTAGATGGTGAGCCT[G/T]Agtgtgtgtgtgtgt | 225743 |
rs52537963 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77544268 | GATGCCTCCTGCAAG[A/G]GAGGAGCCAATGGGT | 225743 |
rs52574575 | snp | G/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77475432 | ctctccctttcttcc[G/T]ccctccctctctccT | 225743 |
rs107910790 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77505528 | GGGATTAGTAATGAT[A/G]CTTGTCAAATTTTCT | 225743 |
rs108395450 | snp | C/T | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77468501 | TTTCAGAAGAGGGAG[C/T]ACCACCCTGTCGAGT | 225743 |
rs108914264 | snp | A/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77522965 | CGGGGCGCTTGCCTC[A/T]CACTCCAGGGGTGAG | 225743 |
rs211704567 | snp | G/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77493289 | CCGTCAGGTAACTAT[G/T]GCTCTGCTCTCATCG | 225743 |
rs211766913 | snp | A/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77485165 | AAAATGAAATACCAA[A/T]CCATTTATTAAGACT | 225743 |
rs211783800 | in-del | -/A | | | utr-variant-3-prime | Rnf165 | GRCm38.p3 | 18:77462200 | CTTTCCACCAAAAAG[-/A]AAAAAAAAATGTGCT | 225743 |
rs211792875 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77529157 | GTTTGTATTCAAGCC[A/G]GAGAGATTAAAGATG | 225743 |
rs211826331 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77477226 | ACATAACAGGAAGAA[A/G]ACACCCAGGTCAAAG | 225743 |
rs211837155 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77557994 | ACACCAGCACTGATG[C/T]CCTACTCAACTAACA | 225743 |
rs211854794 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77529713 | AAAAGCCTATCTTCC[A/G]CACCTCTGCCCTTGG | 225743 |
rs211861751 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77522487 | GTGTACCCAACTACA[C/T]TCCCATGACTCACAA | 225743 |
rs211874094 | in-del | -/AAAAC | | | intron-variant | Rnf165 | Mm_Celera | 18:77479882 | AGACAAATAAAAGGA[-/AAAAC]AAAAAAAAAACAAAA | 225743 |
rs211890235 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77468966 | TTCATTTAAACTTGA[A/G]CTTCACTAAAACGTT | 225743 |
rs211898185 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77486210 | TAGTTAAGAACACTG[A/G]CTGCTCTTCCAGAGA | 225743 |
rs211939616 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77549499 | GAATGCTTGGGTCCC[C/T]ACTTAGTGGAACTGT | 225743 |
rs211968464 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77499494 | TTTCTAGGCCAAGGG[A/G]TTTTAGACAAGGTCT | 225743 |
rs211984732 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77478069 | GCAAGCTAGTGTAGC[C/T]ATTTTAATGTCTGAC | 225743 |
rs212007036 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77550205 | TGGCACATGAATGCC[A/G]AGGCTTGCCTAGCGG | 225743 |
rs212029394 | snp | A/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77500395 | CACACACAAATTTTT[A/T]AAAAAAACATTGTTT | 225743 |
rs212040583 | snp | A/G | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77492595 | AAGTCCACATCAGAA[A/G]GACATCTTTCAGAAG | 225743 |
rs212108398 | snp | A/C | | | intron-variant, downstream-variant-500B | Rnf165, LOC105246499 | Mm_Celera | 18:77507323 | CCAGCTATTTTGCTG[A/C]CTAAGGCATATTTAA | 225743 |
rs212115397 | in-del | -/GTC | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77468706 | TCACACCTAAGACTT[-/GTC]GGTCTGAGGCCCCTG | 225743 |
rs212127917 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77528567 | TCTGGCTTTTCTCTG[A/G]GCCTCTGAATTGCTC | 225743 |
rs212143103 | in-del | -/ACAA | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77466365 | GCCCACAGGACTGAT[-/ACAA]ACAGTGATGTATCTG | 225743 |
rs212150607 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77542626 | AATTCAGCCACACAG[A/G]GGAGGTTGCTCTTGC | 225743 |
rs212155560 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77475968 | CAGTGGACCAGTTCT[C/T]CCAAGCACCCTTGGG | 225743 |
rs212184267 | snp | A/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77521597 | AGGATCCCACGGCAT[A/T]CCCTATGTAGAGATA | 225743 |
rs212197194 | snp | A/G | | | intron-variant, upstream-variant-2KB | Rnf165, LOC105246499 | Mm_Celera | 18:77514811 | AAATGTGGGGCTCAG[A/G]ACTCTTGCTTTCTTC | 225743 |
rs212225974 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77468047 | GACTGCAGCCTGCCA[C/T]GATGCCTCTTCTACT | 225743 |
rs212304798 | snp | A/C | | | intron-variant | Rnf165 | Mm_Celera | 18:77557381 | GGAACGAAGACTGGG[A/C]GACCAGTCACCCTGA | 225743 |
rs212305040 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77498411 | CAGCCCACACCCAGC[C/T]TCTCCCAGACGTGCT | 225743 |
rs212307337 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77491253 | ATATGCTTGGGCCAG[A/G]AAGTGGCACTATTAA | 225743 |
rs212351428 | in-del | -/ATGA | | | intron-variant | Rnf165 | Mm_Celera | 18:77521916 | TGGACAGATGGATGG[-/ATGA]ATGGATGCATGGGTG | 225743 |
rs212372331 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77483443 | GGAAACTATAATCAG[A/G]ATATATTATGTGAGA | 225743 |
rs212386364 | snp | A/T | | | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77514252 | GAGATGTTGCTAAAA[A/T]CACCATGACGAACAC | 225743 |
rs212396751 | in-del | -/GAATGGTTAAG | | | intron-variant | Rnf165 | Mm_Celera | 18:77534798 | AGGAAGGTGCAGAAT[-/GAATGGTTAAG]GATGCAGTGAGTGGG | 225743 |
rs212422439 | snp | A/T | | | utr-variant-3-prime | Rnf165 | Mm_Celera | 18:77458656 | GCCATGTTTTTTTTT[A/T]ATTTTTTTGTGTTTT | 225743 |
rs212464004 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77528215 | ACCTCCAAAAAGGCC[A/G]TGACCCCCAGGCTGA | 225743 |
rs212500322 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77475228 | CAGGATAGTGCCCAG[C/T]TCCACTGAGTGAATT | 225743 |
rs212525830 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77525866 | TTTTGAAAGGCATAT[A/G]TACTGGCTGGTTTTG | 225743 |
rs212542727 | snp | G/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77490565 | TGCTTGTGAGTCACT[G/T]CCAAGGACGGGCAGA | 225743 |
rs212568865 | snp | C/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77463966 | CAAAGAGACACAGGT[C/G]CAGACCAGAGAATGA | 225743 |
rs212571256 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77471289 | CCAACACTCCATAAA[C/T]GACACAAGCAAACCG | 225743 |
rs212577478 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77533108 | AGAAACACGAGGGGC[C/T]GAACTTACCACGGGA | 225743 |
rs212589238 | snp | A/C | | | intron-variant | Rnf165 | Mm_Celera | 18:77518782 | CTCCGAAGGCTGTAA[A/C]CGTGACTTCCACTGA | 225743 |
rs212617053 | snp | G/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77482699 | ACCCATACCCGACAC[G/T]GCTTGGGTGACCAAG | 225743 |
rs212635307 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77465111 | GATGGTAGGAAGCAG[A/G]AGTTGGACCTAGCTT | 225743 |
rs212662220 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77487056 | ACTCGGGATGGGTCG[A/G]GTAGAGGCAGAGTGT | 225743 |
rs212674486 | in-del | -/TCTC | | | intron-variant | Rnf165 | Mm_Celera | 18:77533995 | CTCTCTGGGTCTGGG[-/TCTC]TCTCTTTCTCTTTCT | 225743 |
rs212682559 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77553881 | CAGGCCCAGCCCTAC[C/T]TGGGAACCGGTTCTC | 225743 |
rs212705474 | snp | C/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77494910 | GAGCTTTGACTGTGA[C/G]TTTTCTTATTCTGGG | 225743 |
rs212728353 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77479622 | GAAGCAGAAGGAACA[C/T]TGCCCAATTTATTTT | 225743 |
rs212793801 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77562200 | CAAATGGCATTCTGA[A/G]GCAACTCCTTGGGAC | 225743 |
rs212862433 | snp | A/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77525034 | CCCTTTCACAGGAGG[A/T]AGGGAGGAGACAAGA | 225743 |
rs212912999 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77501766 | AACCAAGTCCTGTGG[C/T]CGTGTGGTTCATTGA | 225743 |
rs212913838 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77470791 | TGTTTCTCACGTTGT[A/G]GGTCCTGACCCTTTT | 225743 |
rs212929260 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77558851 | GAAGTCTCTGGTTTG[C/T]TGAGCATTGCTCGTT | 225743 |
rs212946535 | in-del | -/GTTGGTTGGTTG | | | utr-variant-3-prime | Rnf165 | Mm_Celera | 18:77461742 | AAGATTGGGGCTGTC[-/GTTGGTTGGTTG]GTTGGTTGGTTGGTT | 225743 |
rs212965890 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77552302 | CTCCTCTCCCAGCAT[A/G]TGTCCATGTTAAGAC | 225743 |
rs212985565 | snp | C/T | | | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77511106 | AACACCGTCCAGCAC[C/T]GTTGGCAACTGTCTC | 225743 |
rs213036919 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77536854 | TGGTTACCAGGGGAG[A/G]AGAATCTTTCCTTGC | 225743 |
rs213049160 | in-del | -/CACACACACG | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77500385 | ACACACACACACACA[-/CACACACACG]CAAATTTTTAAAAAA | 225743 |
rs213049967 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77494477 | AGTTGCTGGAGGAAT[A/G]GGGTTGCCTTTGAAG | 225743 |
rs213064763 | in-del | -/TCCCCCCCGGT | | | intron-variant | Rnf165 | Mm_Celera | 18:77552168 | AGAGAGGCATGGTGG[-/TCCCCCCCGGT]CACCCCACCCTCAAC | 225743 |
rs213089166 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77537344 | TTTGTTTCCCTGCAG[C/T]TGTCCCAGCCATTGC | 225743 |
rs213112384 | in-del | -/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77535039 | GGGCACAACACTTTC[-/T]TTAAGACGCTGTCTG | 225743 |
rs213130804 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77487901 | TTGACTGAGACAGCG[C/T]GGAGTAAGGAGACCC | 225743 |
rs213136374 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77564506 | AGAGCCCAGCTCACC[A/G]GTCATCCGCCTTAAG | 225743 |
rs213148942 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf165, LOC105246499 | Mm_Celera | 18:77516267 | GAGCTGAGACACTTG[C/T]TCCCTTAAGATGCTT | 225743 |
rs213150981 | in-del | -/CC | | | intron-variant | Rnf165 | Mm_Celera | 18:77544792 | ACTGGAGTGAGAAAA[-/CC]CACATGCAATGACAT | 225743 |
rs213152299 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77523069 | CCAATCTTAAAACTG[A/G]TGTCCTTGGTTAGAC | 225743 |
rs213212820 | snp | G/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77480115 | AAGATTTGTCTGCTC[G/T]CTCCATACCTATTCA | 225743 |
rs213225775 | snp | G/T | | | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77508283 | CCAGCTCTACAATGG[G/T]TCTCACAACCAGTGC | 225743 |
rs213271382 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77462846 | AAATGCAGGCGGGGG[C/T]GGCAGGGGAGGGGAG | 225743 |
rs213296661 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77556393 | TTGTCTTAGCTGCAC[C/T]CCTCCTCTATCCCCT | 225743 |
rs213297374 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77551699 | TTGTGGAAGCCCCTC[A/G]TAGAGCTCTGAATGA | 225743 |
rs213303040 | snp | A/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77505767 | CTTCCGGGAACTGGT[A/T]GCCCACTTTGTGGGA | 225743 |
rs213309315 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77497205 | TCCTAGCTGAGCCAA[C/T]GGCAAATAGTCGTCG | 225743 |
rs213316198 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77559771 | CACATCTGAGACTCA[A/G]TATTGGGTTGTACAC | 225743 |
rs213320445 | snp | C/T | | | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77508713 | CTCACCAAGGGCCAG[C/T]GGGGCTCCCCTAAAG | 225743 |
rs213347179 | snp | G/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77549044 | ATGCCCTGGAGGGGT[G/T]GGGGGGAGATGCCAA | 225743 |
rs213368621 | in-del | -/GG | | | utr-variant-3-prime | Rnf165 | GRCm38.p3 | 18:77460837 | TAGGTGATGTGGGGC[-/GG]GGGGGGGGGGCATGG | 225743 |
rs213395152 | snp | A/C | | | intron-variant | Rnf165 | Mm_Celera | 18:77498636 | ACCCGTCCTCCCACC[A/C]TAGTGCTCCAGCTTC | 225743 |
rs213407011 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77542016 | GCTAAGGCTGTGCTC[C/T]CCGAAAGCGCTGCAA | 225743 |
rs213432673 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77491298 | CTGGAGTAGGTATGT[C/T]ACTGTGGGCTTTAAT | 225743 |
rs213517064 | snp | G/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77520143 | AAATCTCTGACATAT[G/T]CGCTTTTTGTGACAC | 225743 |
rs213521452 | in-del | -/T | | | utr-variant-3-prime | Rnf165 | Mm_Celera | 18:77460450 | AGCATACGAGGACAC[-/T]TAAGACTGGCTACGG | 225743 |
rs213537847 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77466866 | TTTGCGCAGGAAGCC[A/G]GCTCACTGCCCCAGC | 225743 |
rs213594169 | snp | A/G | | | utr-variant-3-prime | Rnf165 | Mm_Celera | 18:77457205 | AGAAATCCCCACACC[A/G]TGGTCTGGGTCTTCT | 225743 |
rs213607395 | in-del | -/A | | | intron-variant | Rnf165 | Mm_Celera | 18:77477087 | AGGAAACAAAAGAAG[-/A]AATGGGTACCTCAGT | 225743 |
rs213625646 | snp | C/T | | | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77514018 | GACTCATCTGTTTAG[C/T]GGGGATAATGCTGAG | 225743 |
rs213666384 | snp | C/T | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77492570 | CAAAGCCCTTCTGAC[C/T]GAGAGGTTGAAGTCC | 225743 |
rs213725693 | in-del | -/ACACACAC | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77524052 | CATCTCTAAGCCACT[-/ACACACAC]ACACACACACACACA | 225743 |
rs213765889 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77526584 | TGAGTGGACGAGAAT[A/G]GAACCCTAGACCCAG | 225743 |
rs213791392 | in-del | -/C | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77527642 | AAGAAGAGTCTGGGG[-/C]CCCCCAAACAGTATA | 225743 |
rs213821387 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77519601 | TCCAAACACGAGAGT[C/T]GAATTGAATAACTGA | 225743 |
rs213847647 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77555731 | TGGCTCTCCACCTCA[C/T]CTCTGATAGTTGCTC | 225743 |
rs213849762 | in-del | -/CG | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77544162 | GCAAGCACAAGCACA[-/CG]TGCACACACAGACAC | 225743 |
rs213864952 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77466297 | GTCTTTATGTAATTG[A/G]ACCAAGAATTGTTTT | 225743 |
rs213916014 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77546109 | CAGTAGGGAAACAAC[A/G]TATTTCCCAATTCTT | 225743 |
rs213921199 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77532881 | AAAAAACCAAATATA[C/T]ATTCTAGATAATTTA | 225743 |
rs213921909 | snp | C/T | | | upstream-variant-2KB | Rnf165 | Mm_Celera | 18:77567709 | CAGCTAATGAGTGTA[C/T]TGTGAAATTACTTAG | 225743 |
rs213940880 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77495578 | CAAGCCAGCATCCCT[C/T]CCCCCCACCCACCCC | 225743 |
rs213964969 | snp | A/C | | | intron-variant | Rnf165 | Mm_Celera | 18:77533578 | CTGCCAGCCCTTCTG[A/C]CCCAGGACATGAGGG | 225743 |
rs213990720 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77496459 | TAGCTCAATTAACCA[C/T]GCATATGCCAGAATC | 225743 |
rs213992398 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77489181 | GGAGCCAGGAACCTC[A/G]ACCAGCAATGCAAGA | 225743 |
rs213993037 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77482462 | CACTGAACAGGTATG[A/G]GTTGAGCTGGTGCCT | 225743 |
rs214005583 | in-del | -/CT | | | intron-variant | Rnf165 | Mm_Celera | 18:77529867 | CAGTCTGTCTATTAC[-/CT]CTCGTAGCAAAGGTC | 225743 |
rs214044345 | snp | A/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77486377 | AAGAAAATATGTAGG[A/T]ACCACTGTACCCTGA | 225743 |
rs214045470 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77527089 | TTATGCATCAGTCCT[A/G]CTCATTGAGGCTGGC | 225743 |
rs214077631 | snp | G/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77536548 | ATCCAGAATGTGAGT[G/T]TGCACTTGCCTATGC | 225743 |
rs214106543 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77486857 | GTACCAACCATAACA[C/T]AGTTAATAAACTGCA | 225743 |
rs214142434 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77554701 | TCCCTTGCCTTCCCA[C/T]CCTGTCCTTTATTTC | 225743 |
rs214177848 | snp | A/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77504107 | CAGCATGGACCAGCC[A/T]GACTAAGCACTTAGA | 225743 |
rs214181857 | snp | A/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77504857 | GGCTAGCTCTGGCTC[A/T]GAGAAGGAGATTATA | 225743 |
rs214218968 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77538236 | TCATCAAATGTGCAT[A/G]CTCTGGAGAGTCAAA | 225743 |
rs214222747 | snp | C/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77531104 | TCTCTATGTATGTGT[C/G]TATGTCTCTGTGTGT | 225743 |
rs214280568 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77532546 | AGACCCTCTGCTTTC[A/G]TATGGCCTATTTTGG | 225743 |
rs214295282 | snp | G/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77493309 | TGCTCTCATCGGCCC[G/T]GAGAGGCCGATTTCC | 225743 |
rs214311374 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77481925 | CCCAGAAAGGCAGAT[A/G]TGGTATGTATCCGCT | 225743 |
rs214319207 | in-del | -/CCCC | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77534251 | CAAGATTCCAAACAG[-/CCCC]CCCCCCCATCACTGC | 225743 |
rs214334535 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77535252 | CATGTTCCAACCCTT[C/T]CACCTCTGAAATACA | 225743 |
rs214371591 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77493650 | GTAGCCAGGGCTGGT[A/G]TCCTGACTCCATTTG | 225743 |
rs214373319 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77529737 | CCCTTGGGCAAAACT[A/G]GTTACTCCCGTCTCT | 225743 |
rs214383677 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77472991 | CTTCTGGTGTCTGAC[A/G]ACAGTGACAGTGTGC | 225743 |
rs214412344 | snp | G/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77478269 | ACCCTCATGCACTGA[G/T]AGTGGGAGATTTTAA | 225743 |
rs214437769 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77523198 | ACAGACACATGCATA[C/T]GCTTGTGAGCATGCA | 225743 |
rs214442237 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77522345 | TATCAGATCGTATGT[A/G]GGTCAGGGGTAAGGT | 225743 |
rs214501680 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf165, LOC105246499 | Mm_Celera | 18:77515332 | GTTCTTCTGGTGTTA[C/T]TAGCAATGTGAGAGC | 225743 |
rs214542772 | in-del | -/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77489704 | CAAGCCTCTTGTCTC[-/T]TTTTTTCCTGACTGT | 225743 |
rs214570962 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77500543 | CAAGACATCCCAGGG[C/T]TACACAGAGAAACCC | 225743 |
rs214623127 | snp | C/T | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77492334 | CTGCATCTTTAGAAA[C/T]CCCCATGGAAAAGGC | 225743 |
rs214623355 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77483610 | TTGTAGTCAATTTTG[C/T]GTGTGTGAAAAAGGC | 225743 |
rs214682971 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77484113 | AAGCCCCGCCCATCC[C/T]GGCCCCGCCCCCTCC | 225743 |
rs214717665 | in-del | -/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77562097 | TTCTGGTTTGTTTTG[-/T]TTTTGTTTTGTTCTG | 225743 |
rs214769587 | snp | A/C | | | intron-variant | Rnf165 | Mm_Celera | 18:77521963 | ATGGATGAGAGGTTA[A/C]GACATAATGCAAGGC | 225743 |
rs214815501 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77530261 | ACATTTAAGTATGAC[A/G]TATCTTCTACCTTCT | 225743 |
rs214833082 | snp | A/G | | | upstream-variant-2KB, missense | Rnf165 | Mm_Celera | 18:77565645 | GCGCAGACAGGCAGC[A/G]AGTGCACACGACCCA | 225743 |
rs214851673 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77479458 | GATCAGATAAGCAAT[C/T]TAAACTTATAACCCC | 225743 |
rs214880879 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77523981 | TGTAACAAGAGGAAT[C/T]ACACAAACTCAGACA | 225743 |
rs214894615 | snp | C/T | | | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77512321 | ACGATTATACTTGGA[C/T]ATGATCTTGACAGCC | 225743 |
rs214931097 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77470121 | AACTCACAATCCTCC[C/T]GCCTCATCCTCCAAA | 225743 |
rs214962200 | snp | C/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77504234 | ATTTGGTGTGAGCTT[C/G]CTGAGTAACAGTTTG | 225743 |
rs214993288 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77550444 | GGCCATAAAGAAGAC[C/T]GAGTGTATCTGGCTC | 225743 |
rs215051154 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77531830 | AGTAGCCCAAAATTA[C/T]AGACTGTTGTCAAGG | 225743 |
rs215055299 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77534341 | GGTGAGGTGGTGACG[C/T]TTCTCTTGCCTGTGC | 225743 |
rs215066957 | snp | C/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77481190 | ATTAATAAGAGGAAC[C/G]TCATACAACTGAAAA | 225743 |
rs215107345 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77558079 | CTCTGCCAAGTTCCA[C/T]GTTTATCCGCATACT | 225743 |
rs215122203 | in-del | -/CC | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77492978 | CATTGGTTCCAGGAG[-/CC]CCCCCCCCCGCCCCT | 225743 |
rs215132944 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77528769 | CTCTCTCTCAACTCT[A/G]CTGAGCTGCTGCTCT | 225743 |
rs215156895 | snp | A/C | | | upstream-variant-2KB | Rnf165 | Mm_Celera | 18:77566553 | GTCAGAAAACACATA[A/C]GTTCACCACACAATT | 225743 |
rs215167836 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77518802 | ACTTCCACTGAAAGC[A/G]ATGCATGTATGCATT | 225743 |
rs215246572 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77468825 | CTTCCACTGAGGACA[A/G]GCAGTGGACAAACTC | 225743 |
rs215258038 | snp | C/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77545412 | TGGGAAAGGGGACGA[C/G]AGGGTAGGGGGATGG | 225743 |
rs215262981 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77519463 | GGTGGACAGGAGCAG[A/G]TGTCATAGCCTCCCA | 225743 |
rs215274695 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77506544 | CCAGACGCCCCTCTG[C/T]AGCAACTGTCCCCAG | 225743 |
rs215283981 | snp | A/C | | | intron-variant | Rnf165 | Mm_Celera | 18:77561321 | CCGGGTGAGACAAGA[A/C]ATCTGACCTTCTCCA | 225743 |
rs215311995 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77465961 | ATAGTTCAGAATATA[C/T]AGTTTACAGCCTTCG | 225743 |
rs215318396 | snp | C/G | | | utr-variant-3-prime | Rnf165 | GRCm38.p3 | 18:77457634 | GAGAGAGGAGAGAGA[C/G]AGGAGAGAGAGAGGA | 225743 |
rs215332468 | snp | A/C | | | intron-variant | Rnf165 | Mm_Celera | 18:77488062 | GGTTCGCTGTCCTCC[A/C]GCCGCTAGCTGGAGC | 225743 |
rs215378725 | snp | C/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77537838 | GAATGTGTGTCCGTG[C/G]GGCTGGGCTTTGAAG | 225743 |
rs215390992 | snp | A/C | | | intron-variant | Rnf165 | Mm_Celera | 18:77480210 | AGGAAAGGATGAAGT[A/C]CAAGTACCTTTATTT | 225743 |
rs215393076 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77488650 | AGGGGGAAATGTATG[C/T]CTTAGGAGTCTGGAG | 225743 |
rs215422427 | snp | G/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77517067 | TCACAGTCATCCACT[G/T]GCCCCGAGGGATGGG | 225743 |
rs215450248 | snp | A/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77555196 | AAGCTGTGAGAAGAG[A/T]CTTGCCAGCTCTCTA | 225743 |
rs215457473 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77463043 | TAGAGACTCCTGCTG[A/G]CAACTGCCTTTTGCC | 225743 |
rs215478974 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77528288 | AGAGCCTGGCTGTTA[A/G]CCCTACACTGACCTG | 225743 |
rs215488148 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77517812 | ATCCTGTCAAATGCA[C/T]CACTGGGCATCCGGG | 225743 |
rs215488169 | snp | A/G | | | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77508813 | TTCACCAGACAGCTG[A/G]CACATGGCATAAAGA | 225743 |
rs215515852 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77463733 | GCAGGAAGTTTTCAC[A/G]TGGTACGTGTGCCCA | 225743 |
rs215528546 | in-del | -/TT | | | utr-variant-3-prime | Rnf165 | Mm_Celera | 18:77460341 | AATTGGCCACTGTCA[-/TT]TTTTTTTTGGTCACG | 225743 |
rs215569739 | in-del | -/GTATGCATGTGTGT | | | intron-variant | Rnf165 | Mm_Celera | 18:77506851 | GCCAATGCATTCTGA[-/GTATGCATGTGTGT]GTGTGTGTGTGTGTG | 225743 |
rs215617776 | in-del | -/A | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77563464 | AGCTACACAATGAAG[-/A]AAAAAAAAAGATTTG | 225743 |
rs215622823 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77557459 | CCGCTTTGATCCTCA[A/G]TTTCCTTCCAGGTCC | 225743 |
rs215631691 | in-del | -/AGACAGAC | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77497798 | GATAGATAGATAGAT[-/AGACAGAC]AGACAGACAGACAGA | 225743 |
rs215668815 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77534451 | CAAAACAGCCTGGCT[A/G]GGGGCAATGGTATCC | 225743 |
rs215671372 | snp | A/C | | | intron-variant | Rnf165 | Mm_Celera | 18:77484491 | AAAGACAGAGATCTC[A/C]TGAGGACATGCAAAG | 225743 |
rs215699556 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77476992 | AATCTGGAAGTGAGA[C/T]ATTTAGGAATCAAAC | 225743 |
rs215710926 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77526497 | TGGATGTTAGAGAAG[C/T]CAGAAGTCACAGTTC | 225743 |
rs215733308 | snp | A/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77528814 | ATATTCCCGAACTGT[A/T]CTCTCTTCTCCTGTA | 225743 |
rs215735293 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77485024 | ACTCGGGAGGCAGGT[A/G]GATCTCTGTGGATTC | 225743 |
rs215737127 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77476451 | TCACTCCTGGAGACC[C/T]CTGAGCACTGTTTCT | 225743 |
rs215739285 | in-del | -/CCCC | | | intron-variant | Rnf165 | Mm_Celera | 18:77474817 | TTCCACTGAGGAATA[-/CCCC]CCCCCCCCAACACCA | 225743 |
rs215779023 | snp | A/G | | | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77514209 | TACCAGGGCAGGTGG[A/G]CCATTGGTGTGTAGT | 225743 |
rs215796418 | in-del | -/AAAACA | | | intron-variant | Rnf165 | Mm_Celera | 18:77463506 | ACCAACCAAGCAAAC[-/AAAACA]AAACAAAACAAAACA | 225743 |
rs215844077 | snp | A/G | | | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77514589 | GTCTGTCTGCTTGCC[A/G]CCATGCTCACTGCCA | 225743 |
rs215849113 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77554770 | AGAAATGCCACCCTA[A/G]TCTAGTAGCCAGGTC | 225743 |
rs215889314 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77545841 | TACACTCATGTGACT[A/G]GGGAGCACAGCTGTC | 225743 |
rs215899839 | snp | A/C | | | intron-variant | Rnf165 | Mm_Celera | 18:77506389 | AGGCCTTCTCTGAAC[A/C]CAGGTCCCCTCATCT | 225743 |
rs215913328 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77495443 | TATGTGACACCGTCA[A/G]CCCTTTGGCTGTCTC | 225743 |
rs215926265 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77559848 | ACTGCATTCTGTACA[A/G]TTACTGGATTAGTGA | 225743 |
rs215955102 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77531307 | CTCATGGAGTGAAAC[C/T]GTGAGTCCAAACCAA | 225743 |
rs215966587 | in-del | -/CAAAAAAACAAACAAA | | | intron-variant | Rnf165 | Mm_Celera | 18:77500563 | AGAGAAACCCTGTCT[-/CAAAAAAACAAACAAA]CAAACAAACAAACAA | 225743 |
rs215969362 | snp | G/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77533415 | GGGGGTGGGGGAGGG[G/T]GGTAGGTATATCAGC | 225743 |
rs216004704 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77483212 | TTGGGCCTTCTCTTG[A/G]ACTCTTCTCCCGCTG | 225743 |
rs216005718 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77474315 | CTCCTGTCTCTCCCC[A/G]GGGAGACCCTCCTCT | 225743 |
rs216057777 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77475075 | GCCTTCCCTGACCAC[A/G]CTAGCATCTCTGAAT | 225743 |
rs216082237 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77525909 | ACACAGCTGGAGTTA[C/T]CACAGAGAAAGGAGC | 225743 |
rs216104476 | snp | A/C | | | intron-variant | Rnf165 | Mm_Celera | 18:77471524 | AACACAACATGGGAA[A/C]GAGGTTTTAGAAAGT | 225743 |
rs216105553 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Rnf165, LOC105246499 | Mm_Celera | 18:77515037 | AAGATGCCCTTGTTC[-/T]CTGAATGCTCCATGA | 225743 |
rs216115493 | in-del | -/TA | | | intron-variant | Rnf165 | Mm_Celera | 18:77502494 | CAAGAAAATCCCAAC[-/TA]TATAGCCTGAACCTC | 225743 |
rs216135193 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77552399 | GACATAAGGGACTGG[A/G]ACCATGCCTGGCACA | 225743 |
rs216157449 | in-del | -/A | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77533381 | GCCACACTTGGTGGT[-/A]ATGCTATCCTCAGAT | 225743 |
rs216164071 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77502652 | CACCACCACTGTGTG[A/G]TGGTGTGTATATGCA | 225743 |
rs216175278 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77539236 | TCATATCCAGGGGAC[C/T]AGAGTGGGTCTTCAC | 225743 |
rs216176591 | snp | G/T | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77465161 | GATGCTCCCTGGGGG[G/T]GGGTGGGGCGGGGGG | 225743 |
rs216199201 | snp | C/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77489886 | GGAACAGGATGCCCA[C/G]AGGATGCCTTGCTTT | 225743 |
rs216238096 | snp | G/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77499252 | CATGCTTCTGCCGAG[G/T]CACAAGAAACCCTTG | 225743 |
rs216278708 | snp | C/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77494991 | CTATAAAGCAGGTGG[C/G]GCCGGGGTGAGGACA | 225743 |
rs216281127 | in-del | -/A | | | intron-variant | Rnf165 | Mm_Celera | 18:77488444 | GAGTCATTCTGTCCC[-/A]ATTAAAAAATAATTT | 225743 |
rs216284850 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77542480 | CATCAGAATACTGCT[C/T]TCTCTGATCTGTAGT | 225743 |
rs216310363 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77533050 | ATGGCCCTGGCCCAG[C/T]TTGTGCTCACACCCT | 225743 |
rs216311416 | snp | C/G | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77492490 | CCCCTCAAATTACCT[C/G]GCATGAGGAACAGAT | 225743 |
rs216314048 | snp | G/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77482594 | CCTTCTGATCTACAA[G/T]GCTGTCCTGCCTGCA | 225743 |
rs216363694 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77531139 | CTGCCTGCCTGCCTG[C/T]CTGTCTGCGTATGTA | 225743 |
rs216368561 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77470257 | GAGGGGCAGACTAGT[C/T]TCTTGGTGAGGTTAT | 225743 |
rs216368684 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77479971 | TCTTCATGATAAAAG[C/T]CCTGGAGAGATTGGG | 225743 |
rs216428040 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77470747 | CCTCAAGTGTTTGCC[A/G]AATAGCAAGTTCTGT | 225743 |
rs216530134 | snp | A/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77561371 | TCATAAGATGTGGAC[A/T]ACATGAGATTAGAGT | 225743 |
rs216561789 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77535948 | CCACATCTGGAGAGG[A/G]TTTTCTCTACATCTG | 225743 |
rs216609861 | in-del | -/G | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77497929 | ATGGATGGACTGGAT[-/G]GGATGGATGGATGGA | 225743 |
rs216622254 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77536611 | TGTGTGTTGGGGGGG[A/G]GGGTTACTCTGCCTG | 225743 |
rs216681116 | in-del | -/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77544702 | CATAGAATCCGCTAA[-/G]ATGAGATCATAATAG | 225743 |
rs216682590 | snp | G/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77530400 | CAGTAGCCTGCAGGC[G/T]CCCCAGGGCTGGGCT | 225743 |
rs216683581 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77553022 | GACCCAATACCCCAG[A/G]AAAAGAAAGGAAAAC | 225743 |
rs216685771 | snp | C/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77479525 | CCAAAACAGCTCGGG[C/G]CCAAATGTTTTTAGT | 225743 |
rs216694130 | snp | C/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77549441 | GCTTGGATGAGAGCT[C/G]TAGCAGTTTGGGTGA | 225743 |
rs216700194 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77558200 | TCCCAGTCCTCCACA[C/T]AGACTTGATCCTTTT | 225743 |
rs216728368 | in-del | -/AG | | | intron-variant | Rnf165 | Mm_Celera | 18:77521709 | CATGGTGGACACGAA[-/AG]ATGTAATAATTATCT | 225743 |
rs216729660 | snp | G/T | | | intron-variant, downstream-variant-500B | Rnf165, LOC105246499 | Mm_Celera | 18:77507523 | CAAGAAGGGCTCCCC[G/T]TTCATCAGCATCCCC | 225743 |
rs216772169 | in-del | -/GAGAGA | | | cds-indel | Rnf165 | GRCm38.p3 | 18:77457455 | CTTTTCATCTCTCCC[-/GAGAGA]GAGAGAGAGAGAGAG | 225743 |
rs216785064 | snp | A/G | | | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77508164 | AAGGAAAGATAAGAA[A/G]CCTCGGGGCCCAATG | 225743 |
rs216814668 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77479214 | GAAAGAAGGAAGGAA[A/G]GAAGGAAGGAAGGAA | 225743 |
rs216829082 | in-del | -/TG | | | intron-variant | Rnf165 | Mm_Celera | 18:77557497 | TGTCCCCTCAGGCTA[-/TG]GTTATACCTGGAGGA | 225743 |
rs216838106 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77501653 | CCAAGACGCCAAGAC[C/T]GTGGCTTGCTTCCAG | 225743 |
rs216843164 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77528157 | AATGTAAATATCCCT[A/G]TTTTCTAAGGGTCTT | 225743 |
rs216905843 | snp | G/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77529128 | TTTGGGATTAAAGAT[G/T]CGTATAAAAGTTTGT | 225743 |
rs216944366 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77520893 | GGCAGAGGTCCAGCT[C/T]AGAAACAGTCAAGAG | 225743 |
rs216972360 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77467754 | TGTAAGGTCAGCTCC[C/T]AGTGTTGTTCCTCAG | 225743 |
rs217064953 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77504311 | TTGGCATCCTGAAGA[C/T]AGCCATGCATGCGCA | 225743 |
rs217080945 | snp | A/G | | | utr-variant-3-prime | Rnf165 | Mm_Celera | 18:77459961 | GGACACAGCCATCAG[A/G]GGAGCAGCAGGAAAG | 225743 |
rs217088760 | in-del | -/A | | | intron-variant | Rnf165 | Mm_Celera | 18:77527058 | GTTTCTAAAAGCCCC[-/A]GAGAAGGAGGATGGC | 225743 |
rs217095542 | snp | G/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77549081 | CAGGTTAAGGGTGTG[G/T]ACACAACCCTAAGAA | 225743 |
rs217117013 | snp | A/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77498679 | GATTCTGTCCCTCTC[A/T]GGTGACCTCATAATG | 225743 |
rs217120675 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77504815 | AGCTGCTACCTAGCA[A/G]ATCAGCAGGAGGCCA | 225743 |
rs217127226 | snp | C/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77497121 | TGAGGCCACCTTAAG[C/G]CAGTCTTTCCTAGTG | 225743 |
rs217144807 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77548236 | TGATTCTCCCTCTGG[C/T]TCTGAGGTGAGACAT | 225743 |
rs217182153 | snp | A/C | | | intron-variant | Rnf165 | Mm_Celera | 18:77548912 | CGGGACCCAACCAGA[A/C]ACTCAAGCAGGAACC | 225743 |
rs217202660 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77497187 | GATAAGACTGAAGTG[A/G]CTTCCTAGCTGAGCC | 225743 |
rs217204732 | in-del | -/CCCCTTCTTAGAAG | | | utr-variant-3-prime | Rnf165 | Mm_Celera | 18:77461496 | TCCTTTTAAGCCCAT[-/CCCCTTCTTAGAAG]CCCCTCTTACACTCC | 225743 |
rs217231847 | in-del | -/CACACACA | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77523135 | AACCACACATGCACG[-/CACACACA]CACACACACACACAC | 225743 |
rs217238599 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77527145 | AAGGCCTTGGCTGGC[A/G]GCTAACATTCTGGAT | 225743 |
rs217248434 | in-del | -/A | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77500589 | AACAAACAAACAAAC[-/A]AAACAAAAACATCAA | 225743 |
rs217250339 | in-del | -/CACACA | | | intron-variant | Rnf165 | Mm_Celera | 18:77523136 | AACCACACATGCACG[-/CACACA]CACACACACACACAC | 225743 |
rs217296629 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77472659 | ACTTAGACCGGCGAT[A/G]TCAGCATCAGACAAA | 225743 |
rs217300609 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77555687 | GGACAGGTGCTAGCT[A/G]AGTCCTGCTCCCTAT | 225743 |
rs217324699 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77520204 | TATCTACCGCTGAGC[A/G]ACCTCCCAGCCTTTG | 225743 |
rs217328083 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77554834 | ACCAAGCTGAGGTTC[C/T]TTCCCTCACTCCAGC | 225743 |
rs217338223 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77467126 | CTGCCACATCCGCTA[A/G]CCAGCCAGCACACCC | 225743 |
rs217406413 | in-del | -/ACA | | | intron-variant | Rnf165 | Mm_Celera | 18:77497012 | GCCCTTCCTGGTTAT[-/ACA]CATTGACACTCACTC | 225743 |
rs217411168 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77531872 | GCCAGTTCTGCTGTG[C/T]CCTGAGCACAGGGCT | 225743 |
rs217416738 | snp | C/T | | | synonymous-codon | Rnf165 | Mm_Celera | 18:77466764 | CCTGTCCTCCAGCTG[C/T]AGCAGCTCCTGTCAA | 225743 |
rs217440398 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77496537 | AAATTGATTACATAT[C/T]GAAATTCTATTTTAG | 225743 |
rs217447219 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77525929 | GAGAAAGGAGCCTCC[C/T]TTGAGGAAATGCCTC | 225743 |
rs217510765 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77524221 | TGGATCCTTTCAAAG[C/T]CATGCTAGCAAAGGA | 225743 |
rs217564219 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77481259 | CAGCAGCCTTTAGAA[C/T]GAAAAATGTTTGTCT | 225743 |
rs217586248 | snp | A/C | | | intron-variant | Rnf165 | Mm_Celera | 18:77564287 | ACATACACACACAAA[A/C]ACACACATGCACACG | 225743 |
rs217590546 | snp | A/T | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77503659 | GATTTTGGAAGTGCG[A/T]GATTTGGGTGCTTTA | 225743 |
rs217592079 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77517163 | GTGACAGATCTGTTC[A/G]TGTAAGACACCCAGG | 225743 |
rs217637055 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77463120 | GTATCTTTAAATCCT[C/T]ACCCCTAACTCTTCA | 225743 |
rs217669186 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77528904 | CTTTTCTGTCAAAAG[C/T]GTGATGGCACACATC | 225743 |
rs217670576 | snp | G/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77521343 | TCCAGCCACTGTGAT[G/T]ATCAGACTAGACAAG | 225743 |
rs217693483 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77553256 | GTTCTGGTTGTGAGG[C/T]CTGACTGTGCATTCT | 225743 |
rs217720732 | in-del | -/T | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77562122 | GTTCTGTTTTGCAGG[-/T]TTTTTTTTTGTTTGT | 225743 |
rs217729483 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77522090 | TCCAGGCTGGCCAGG[A/G]CTACACAGTCAGACC | 225743 |
rs217741650 | in-del | -/C | | | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | GRCm38.p3 | 18:77507899 | CTGACCACAGCCCCA[-/C]CCCCCACCCTGCAAC | 225743 |
rs217757456 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77493741 | ACAGAAAAAGAAATA[C/T]CTTTTCTCCATTTAA | 225743 |
rs217762789 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77524794 | GCTCTGACTACAACT[A/G]GTCTAGCTGGCTGGT | 225743 |
rs217772770 | in-del | -/A | | | intron-variant | Rnf165 | Mm_Celera | 18:77503635 | GCCCTTCCACTGTCT[-/A]AAACCCGAGATTTTG | 225743 |
rs217830451 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77498825 | CAAGTCTGTAATTCT[A/G]ATTCCACGTCCGCCT | 225743 |
rs217830767 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77517902 | CACCGTGAAGGCCAG[A/G]GAAGGCGACAGGAGG | 225743 |
rs217833683 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77475718 | CAGAAATTGGAGTTC[C/T]CAAACACCAAGGGTC | 225743 |
rs217863483 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77463859 | CAACGCTGCAGACAT[C/T]TGATAAGTCTGAGAG | 225743 |
rs217867869 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77486512 | GGTAAAAGGGAATAG[A/G]GGAAAAGATACTTTT | 225743 |
rs217940509 | snp | C/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77468400 | CCTCGTGAGCTACAA[C/G]GTGGCGGGAGCACCA | 225743 |
rs217951493 | in-del | -/A | | | intron-variant | Rnf165 | Mm_Celera | 18:77468804 | CAAAGGCATCCAGGC[-/A]AACGGCTTCCACTGA | 225743 |
rs217955752 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77544920 | CAGGACCTGCTGGTC[C/T]TTTGAGCCCTTGCTC | 225743 |
rs217970062 | snp | C/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77528437 | CTAGAATGGTTTTCA[C/G]CCTCTGAGACTGGCT | 225743 |
rs218050275 | in-del | -/AGACAGAG | | | intron-variant | Rnf165 | Mm_Celera | 18:77518703 | GACAGACAGACAGAC[-/AGACAGAG]AGAGAACTAGCCTGT | 225743 |
rs218058409 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77487029 | TAGAAACATAGGGCC[A/G]TGGAGTATCTGACTC | 225743 |
rs218060653 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77505178 | TAGATGGGTGGATCT[C/T]GTAGGATGCAAATTC | 225743 |
rs218121103 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77497373 | GCACCCAGATAATCC[C/T]CAGGACAGAGCTAGA | 225743 |
rs218162406 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf165, LOC105246499 | Mm_Celera | 18:77516194 | GCTGACTGCTGCAGC[C/T]ACTTCAACTTCCGGT | 225743 |
rs218178421 | snp | C/T | | | utr-variant-3-prime | Rnf165 | Mm_Celera | 18:77462139 | CCTGATGGGTGGGTC[C/T]TCCCACCCTACCCCT | 225743 |
rs218212153 | snp | C/G | | | intron-variant, downstream-variant-500B | Rnf165, LOC105246499 | Mm_Celera | 18:77507405 | GCAGGGGAGAAGTCC[C/G]GGGACGGGATTTGTA | 225743 |
rs218220814 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77473385 | ATTTACTAAACAGCA[C/T]AACCCCTAGCAACGA | 225743 |
rs218275829 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77474524 | AATTAGGAAAAAGCT[A/G]GGCTGCATTTGGCAG | 225743 |
rs218289081 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77548722 | GGGAGTCAGGGTACC[C/T]GAGAATCCTGCTCTT | 225743 |
rs218331875 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77467302 | GTGGCGCCGTTCTGA[A/G]CTCCTCCCCCGCCTC | 225743 |
rs218355408 | in-del | -/AGGGGGGA | | | intron-variant | Rnf165 | Mm_Celera | 18:77563775 | GGGGCTTGGGGGGGG[-/AGGGGGGA]GGTTAGCCAGTGGGA | 225743 |
rs218392800 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77526792 | TCAGAACATGGGATG[C/T]CCCTGCACACACTGC | 225743 |
rs218447960 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77527371 | AGCAAACCACCCCTG[C/T]TGAAGAATCCCTGTG | 225743 |
rs218469688 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77494780 | CCCATGTGGTTAGGA[C/T]AAGCTATAACATCCT | 225743 |
rs218476221 | snp | C/G/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77555853 | GGGGGCTACACAGCC[C/G/T]GAGGCAGCACACCTC | 225743 |
rs218500730 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77522476 | TGCAGAAGAGCGTGT[A/G]CCCAACTACATTCCC | 225743 |
rs218527794 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77468883 | GGGCCCCTCCTGGTG[C/T]TCGTTCTTCAGGCTA | 225743 |
rs218568486 | snp | A/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77469798 | TGATGACTGTTCCAT[A/T]GTGACGTTGCTCAGC | 225743 |
rs218579394 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77522873 | TATTAATTAATTACC[C/T]CCAGGGGGGTCCTGC | 225743 |
rs218587282 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77552538 | TCCCCCTCGTAACCC[C/T]GTTGGGAGGTCACTA | 225743 |
rs218594099 | in-del | -/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77503010 | TAAAACCCTAAGACA[-/G]CCACCAGAGTGTGGT | 225743 |
rs218600384 | snp | A/G | | | intron-variant, upstream-variant-2KB | Rnf165, LOC105246499 | Mm_Celera | 18:77515574 | GGAGGAGACATGACC[A/G]GCCAGGGCTACAGAC | 225743 |
rs218606637 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77469368 | AAAGGCAGAGAGGTC[A/G]ATGGAAGAAAAATCA | 225743 |
rs218626026 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77462691 | GTTCACGGTTTCCAC[A/G]TCTAGAATAGTCCAT | 225743 |
rs218627077 | snp | C/T | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77497805 | AGATAGATAGACAGA[C/T]AGACAGACAGACAGA | 225743 |
rs218627729 | snp | A/G | | | utr-variant-3-prime | Rnf165 | Mm_Celera | 18:77461112 | AGCACTTTAGCCGAG[A/G]CCAAGTCTACACTGC | 225743 |
rs218639582 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77553418 | GACCATCTCCTGTCT[A/G]CCCTGTCTTCCCAGG | 225743 |
rs218662311 | in-del | -/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77481274 | TGAAAAATGTTTGTC[-/T]TTTTTTTTTTTAACT | 225743 |
rs218675905 | snp | A/G | | | upstream-variant-2KB | Rnf165 | Mm_Celera | 18:77567579 | GGGGAGGGGGGAAAA[A/G]GAGAGGGAGGGAAAG | 225743 |
rs218678401 | in-del | -/GAGG | | | intron-variant, upstream-variant-2KB | Rnf165, LOC105246499 | Mm_Celera | 18:77515461 | ACCAGAAGTACGTAT[-/GAGG]GAGGGAGGGAGGGAG | 225743 |
rs218680091 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77463198 | GGTGGACTGTTGGTG[A/G]TCATCAAGGGGCCCA | 225743 |
rs218681537 | snp | A/G | | | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77512952 | CACCAAGGGAGTCAC[A/G]TGGAATAAAGCCAGG | 225743 |
rs218694161 | snp | A/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77545606 | GTGACCAAGGTCTAG[A/T]CCCGAGGCAGGAAGT | 225743 |
rs218719038 | snp | A/G | | | utr-variant-3-prime | Rnf165 | GRCm38.p3 | 18:77457088 | ATAGGCAAAGGGGAG[A/G]GGGTGCTGGGGAGAA | 225743 |
rs218722385 | snp | A/G | | | upstream-variant-2KB | Rnf165 | Mm_Celera | 18:77566833 | AGGAGAGGAGCAGAA[A/G]CTAGCGGGAACAGTT | 225743 |
rs218729481 | snp | G/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77544442 | TATTCAGGCTCGCTT[G/T]GCTCACCATCCTCTC | 225743 |
rs218737834 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77523461 | TTCCCCAGTCCACAA[A/G]ATGATATTGGCAGCA | 225743 |
rs218750823 | in-del | -/CC | | | intron-variant | Rnf165 | Mm_Celera | 18:77531191 | TCAGTCCCTGTCCCT[-/CC]CCCCCCCCCCGCCCC | 225743 |
rs218797196 | snp | A/G | | | intron-variant, upstream-variant-2KB | Rnf165, LOC105246499 | Mm_Celera | 18:77516441 | AGGGGGGACCATAGC[A/G]GTGCTCATGACTGCT | 225743 |
rs218804324 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77524263 | GCCCAAGGGCCTACC[C/T]GCAACAGCGGTTCCC | 225743 |
rs218844958 | snp | C/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77541141 | CACCCAACCCCCTCC[C/G]TGCTACTTCAGAACT | 225743 |
rs218857533 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77517395 | GTCAATGCATCTCCC[C/T]GAAGGTGTACCATCT | 225743 |
rs218905086 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77493447 | TTTACAGCCCAGAGC[C/T]TCTTTCTGATGCTTC | 225743 |
rs218919729 | snp | C/T | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77549803 | TGTGTCTATGTTCCC[C/T]TTCATGATCATGGGC | 225743 |
rs218962943 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77493838 | TGTAGTAGTGTGACA[C/T]CAGGTCATAACTAGG | 225743 |
rs218978558 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77550735 | CAGACACAGAGTAGA[C/T]CTTCTGTCCCAGCTT | 225743 |
rs218990273 | snp | A/C/G | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77519532 | AGTGGGAGACTCCTC[A/C/G]TGAGCCTTTGGCTAG | 225743 |
rs219017074 | in-del | -/AAAC | | | intron-variant | Rnf165 | Mm_Celera | 18:77480457 | TAAGCTTGTGTGATT[-/AAAC]AAACAAACAAACAAG | 225743 |
rs219025251 | snp | A/C | | | intron-variant | Rnf165 | Mm_Celera | 18:77466180 | TAATGGCCCTCCAGA[A/C]AGATTCTACTTCTAA | 225743 |
rs219037569 | snp | A/C | | | intron-variant | Rnf165 | Mm_Celera | 18:77544016 | CTCTGGGCTTGGGAA[A/C]AACTTCTCAGCTAAT | 225743 |
rs219055528 | snp | A/C/T | | | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77512451 | GGCTTAAACTTAGTT[A/C/T]CTATTAGCAGAGTCT | 225743 |
rs219090393 | snp | C/T | | | downstream-variant-500B | Rnf165 | Mm_Celera | 18:77455993 | CAGGAAGCGCCTAGC[C/T]GGGGACCAAGCAACC | 225743 |
rs219119821 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77495526 | TAACTGGACCTTGTT[A/G]CCTCTGCTAACCTCC | 225743 |
rs219144632 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77500041 | ACATATGTGATTTGG[C/T]TTTTAATTGCCCTGA | 225743 |
rs219165710 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77520059 | AAGGTAACCCAACCA[A/G]CCATCCCAGAGCTAG | 225743 |
rs219174288 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77538011 | GTAAGTTGTGTTGGC[C/T]ATGGTGTTTTTATCA | 225743 |
rs219201116 | snp | A/C | | | intron-variant | Rnf165 | Mm_Celera | 18:77488755 | GATGCAGGTGCAGGG[A/C]AGGCCCAGGTCACCT | 225743 |
rs219261819 | in-del | -/TGTCTGTATGTATGTA | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77530893 | GCCTGTCTGTCTGTC[-/TGTCTGTATGTATGTA]TGTATGTATGTCTCT | 225743 |
rs219316344 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77490626 | ACAGTAGACTTCTCT[A/G]GGCCTCATTTTGTCT | 225743 |
rs219320778 | in-del | -/C | | | intron-variant | Rnf165 | Mm_Celera | 18:77563515 | CTCTATCATCACACA[-/C]AAAAAAACTGCAGTC | 225743 |
rs219325587 | in-del | -/T | | | intron-variant, nc-transcript-variant | Rnf165, LOC105246499 | Mm_Celera | 18:77510191 | CCCAGAGGTCCCCCC[-/T]GCCCAGATCTGTTCA | 225743 |
rs219337800 | in-del | -/A/AA | | | intron-variant | Rnf165 | Mm_Celera | 18:77542939 | GCCTTAATTCTTGGG[-/A/AA]AAAAAAATGCTGAAG | 225743 |
rs219404228 | in-del | -/C | | | intron-variant | Rnf165 | Mm_Celera | 18:77552857 | TCAAGGACAGAGAAG[-/C]CCCCCCTCCCCACGG | 225743 |
rs219423714 | snp | A/C | | | intron-variant | Rnf165 | Mm_Celera | 18:77526109 | CTCTATGGCCTCTGC[A/C]TCAGCTCCTGCTTCC | 225743 |
rs219424905 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77518254 | GACCCCATGCTGGGT[A/G]TGGAGCGACACCCTG | 225743 |
rs219428188 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77489726 | CCTGACTGTAAACGA[C/T]GTGACCAGCCACCTA | 225743 |
rs219431758 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77479303 | aagaaagaaagaaag[A/G]aaggacatagcaaca | 225743 |
rs219437061 | snp | A/G | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77490454 | CGGTCAGGAAAGAAG[A/G]ACCCAGCCTCGCTCG | 225743 |
rs219448439 | in-del | -/AA | | | intron-variant | Rnf165 | Mm_Celera | 18:77478498 | ACTTACTCCTGAATG[-/AA]AAAAAAAAAATGAGT | 225743 |
rs219466701 | snp | A/T | | | downstream-variant-500B | Rnf165 | Mm_Celera | 18:77456028 | AGCCTTTGGGGAAAT[A/T]CATTGGCCAACTGAG | 225743 |
rs219477772 | snp | C/G/T | | | intron-variant | Rnf165 | GRCm38.p3 | 18:77519135 | TTCCCAGGAAAGATG[C/G/T]GCCTATGTATTTAGA | 225743 |
rs219485093 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77496004 | GGAGCCAAAACCCAG[A/G]AGGGGATTGCTGCTT | 225743 |
rs219525353 | snp | A/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77481888 | GGAAGTGGAAAAATC[A/G]TCCTGTGGGAGGGAT | 225743 |
rs219540143 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77496725 | GTGAAGTATTGATGA[C/T]GGCCATGAAAACACA | 225743 |
rs219542263 | in-del | -/AA | | | intron-variant | Rnf165 | Mm_Celera | 18:77563463 | AGCTACACAATGAAG[-/AA]AAAAAAAAAAGATTT | 225743 |
rs219577626 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77487619 | TGGGCATGGTGCAGC[C/T]AGCAGGAAGAGGTCA | 225743 |
rs219577893 | snp | A/C | | | intron-variant | Rnf165 | Mm_Celera | 18:77495218 | GTTTGTAGAAATAAA[A/C]AAGAAAAGAAAAAGG | 225743 |
rs219611628 | snp | G/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77545919 | CCCACCCCCAACGAT[G/T]TTCAAGTCACTGTAT | 225743 |
rs219632045 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77488211 | TCTGGGGCCTCGCCA[C/T]CTATACTGAAGCATA | 225743 |
rs219655385 | snp | C/T | | | intron-variant | Rnf165 | Mm_Celera | 18:77464252 | AGTCACGATGATCTG[C/T]CTGCTGAAGGATCCG | 225743 |
rs219664822 | in-del | -/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77530286 | CCTTCTTAAGCTCTA[-/G]GAAAAAAAATCCATA | 225743 |
rs219708852 | snp | C/G | | | intron-variant | Rnf165 | Mm_Celera | 18:77545514 | AGGCTTGTCTCTGCT[C/G]GGGAGGCCACCTCTG | 225743 |