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 |