SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6282063 | snp | C/G | 0.5 | 0 | intron-variant | Rnf114 | Mm_Celera | 2:167498342 | AATCTCAGCTGCAGG[C/G]GAGCACATAACTAGG | 81018 |
rs13460986 | snp | A/T | | | utr-variant-3-prime | Rnf114 | Mm_Celera | 2:167515602 | GTGGAGGCAGTGGTA[A/T]AGCCAGGGTCATACC | 81018 |
rs13460987 | snp | C/T | | | synonymous-codon | Rnf114 | Mm_Celera | 2:167512594 | GGAGCATATCCAACG[C/T]CGTCACCGCTTTTCC | 81018 |
rs13460988 | snp | A/G | | | utr-variant-3-prime | Rnf114 | Mm_Celera | 2:167515653 | CCTGCACAGTCGAGG[A/G]AGGCGGTCTGCTGAG | 81018 |
rs13460989 | snp | G/T | | | utr-variant-3-prime | Rnf114 | Mm_Celera | 2:167514784 | ATTGTGCATTAGGTG[G/T]GAGCCCTTGACTCTT | 81018 |
rs13460990 | snp | C/T | 0.497778 | 0.0332592 | utr-variant-3-prime | Rnf114 | Mm_Celera | 2:167514733 | TCATTGACCAATGAA[C/T]CGGGTCCTGGCTGTC | 81018 |
rs27260560 | snp | A/G | 0.231111 | 0.249285 | downstream-variant-500B | Rnf114 | Mm_Celera | 2:167516649 | GTCTCAGCCCTGACT[A/G]AGGACATGTTAGAAT | 81018 |
rs27260561 | snp | A/G | 0.142012 | 0.225474 | downstream-variant-500B | Rnf114 | Mm_Celera | 2:167516604 | GTCCCACAGGGACCT[A/G]AATAAAGCCCAGAGA | 81018 |
rs27260562 | snp | C/T | 0.297521 | 0.245442 | downstream-variant-500B | Rnf114 | Mm_Celera | 2:167516529 | GTGTACAGAACCCTG[C/T]ACTGGATGCTGCCTG | 81018 |
rs27260563 | snp | C/T | 0.244898 | 0.249948 | downstream-variant-500B | Rnf114 | Mm_Celera | 2:167516475 | CTGTGCATGTGTGCA[C/T]TGTGTCAGTTGCTGA | 81018 |
rs27260564 | snp | A/G | 0.391111 | 0.206368 | downstream-variant-500B | Rnf114 | Mm_Celera | 2:167516182 | CCAGTAAGCTGCAAT[A/G]TTTTCATTTAAACAG | 81018 |
rs27260565 | snp | C/G | 0.231111 | 0.249285 | utr-variant-3-prime | Rnf114 | Mm_Celera | 2:167516080 | TCCTTCATCACACTC[C/G]CTGTTTCTAATATGA | 81018 |
rs27260566 | snp | G/T | 0.231111 | 0.249285 | utr-variant-3-prime | Rnf114 | Mm_Celera | 2:167516046 | CACAGGTGTGCCACA[G/T]TGCAGCAGGGACCTC | 81018 |
rs27260567 | snp | A/C | 0.124444 | 0.216185 | utr-variant-3-prime | Rnf114 | Mm_Celera | 2:167515936 | GGATCATTTTCCCAA[A/C]GTTACTGCTTCTTCA | 81018 |
rs27274368 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Rnf114 | Mm_Celera | 2:167515913 | CCAGATGCCAGCAGA[A/G]TCGGACAGGATCATT | 81018 |
rs27274369 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Rnf114 | Mm_Celera | 2:167515765 | CAGGACAGACCCTCT[A/G]CCAGGCCTGGGGCTT | 81018 |
rs27274370 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Rnf114 | Mm_Celera | 2:167515733 | AGCACAAGGAAGAGC[A/G]CCTCCAGTCAGTTCC | 81018 |
rs27274371 | snp | A/C | 0.231111 | 0.249285 | utr-variant-3-prime | Rnf114 | Mm_Celera | 2:167515692 | GAGCAGCAGCTATAA[A/C]AGCTGGAAATGCAGT | 81018 |
rs27274372 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime | Rnf114 | Mm_Celera | 2:167515657 | CACAGTCGAGGGAGG[C/T]GGTCTGCTGAGGCTT | 81018 |
rs27274373 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Rnf114 | Mm_Celera | 2:167515643 | AAGTTAGGCCCCTGC[A/G]CAGTCGAGGGAGGCG | 81018 |
rs27274374 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Rnf114 | Mm_Celera | 2:167515621 | CAGGGTCATACCTGG[A/G]AAGTTAAAGTTAGGC | 81018 |
rs27274375 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Rnf114 | Mm_Celera | 2:167515365 | TTCATGTGTAAGTAG[A/G]GAGAAGGTGTAGGGT | 81018 |
rs27274376 | snp | A/T | 0.124444 | 0.216185 | utr-variant-3-prime | Rnf114 | Mm_Celera | 2:167515249 | TCCCTACACCTGCAC[A/T]TCTGTACACCTGAGG | 81018 |
rs27274377 | snp | A/G | 0.244898 | 0.249948 | utr-variant-3-prime | Rnf114 | Mm_Celera | 2:167515164 | TCTGCAGTTTACTGG[A/G]CCAGGGCTCTGCTCC | 81018 |
rs27274378 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Rnf114 | Mm_Celera | 2:167515028 | TACAGGATCTTAATC[A/G]CATTCATCCTGTTGC | 81018 |
rs27274379 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime | Rnf114 | Mm_Celera | 2:167514795 | GGTGTGAGCCCTTGA[C/T]TCTTGCACCTCACAT | 81018 |
rs27274380 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Rnf114 | Mm_Celera | 2:167514722 | GCAGCGCTCCATCAT[C/T]GACCAATGAATCGGG | 81018 |
rs27274381 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf114 | Mm_Celera | 2:167514596 | TAGACACTCTTGGGA[A/G]GCTCTTTTGAAGTGA | 81018 |
rs27274382 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Rnf114 | Mm_Celera | 2:167513891 | CAGAGCTAGGTATCA[A/G]CATCAGATGTCTTAC | 81018 |
rs27274383 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf114 | Mm_Celera | 2:167513867 | TGGGATGCAATCTGC[A/G]TGCATGGACAGAGCT | 81018 |
rs27274384 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf114 | Mm_Celera | 2:167513793 | TGTACTATTTTCTGG[A/G]CCATTCACTTTCCAT | 81018 |
rs27274385 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Rnf114 | Mm_Celera | 2:167513669 | GCCTTGCTTGGTTTT[G/T]GGGCACTGAAGCCTC | 81018 |
rs27274386 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Rnf114 | Mm_Celera | 2:167513064 | GGAGTGTAAAGACAG[A/T]AACACAAACCAGGGT | 81018 |
rs27274387 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf114 | Mm_Celera | 2:167513003 | GCTGCCTGGAAGTAC[A/G]AGTGTGGCTTAGCCC | 81018 |
rs27274388 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf114 | Mm_Celera | 2:167512941 | GATGGAAATGGCTCT[C/T]GAGGGGCTTTACGGG | 81018 |
rs27274389 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf114 | Mm_Celera | 2:167512893 | CTTAGTTGGATTCCA[C/T]TCCAGTCAGCTGCCC | 81018 |
rs27274390 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf114 | Mm_Celera | 2:167512732 | GCCAGAGGGAAGCTG[C/T]ACGTGTCTCTCTTTG | 81018 |
rs27274391 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Rnf114 | Mm_Celera | 2:167512597 | GCATATCCAACGCCG[C/T]CACCGCTTTTCCTAC | 81018 |
rs27274392 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf114 | Mm_Celera | 2:167512408 | TAGAGTGACCACGCA[C/T]TGTACCTGGGCTTGT | 81018 |
rs27274393 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Rnf114 | Mm_Celera | 2:167512381 | TTTCTGGGTTGCTTC[A/C]TGTTTATGGAGTAGA | 81018 |
rs27274394 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Rnf114 | Mm_Celera | 2:167511802 | ATTAAGCCATGTACA[G/T]CCCAGACGCTGTCAG | 81018 |
rs27274395 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Rnf114 | Mm_Celera | 2:167511281 | TGATCAGGAAGGACT[C/T]GTGGAGCACTGCAAA | 81018 |
rs27274396 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf114 | Mm_Celera | 2:167511121 | TTGTTCATGTCAGTG[C/T]GTCTGATTTGCAAGC | 81018 |
rs27274397 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Rnf114 | Mm_Celera | 2:167511042 | GGAGGGTTTAGGTGT[G/T]TGGATTTGGAGAATT | 81018 |
rs27274398 | snp | A/G | 0.231111 | 0.249285 | missense | Rnf114 | Mm_Celera | 2:167510906 | ATCCGGGCCCATGTG[A/G]CGTCATGTTCCAAAT | 81018 |
rs27274399 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Rnf114 | Mm_Celera | 2:167510849 | TGAACGTCTCACTAA[A/C]TATGGGTCCTGCTCT | 81018 |
rs27274400 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf114 | Mm_Celera | 2:167510818 | TTTCTTGCCCTTGGT[C/T]TGGGATCACATCTTA | 81018 |
rs27274401 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf114 | Mm_Celera | 2:167510656 | TTTTAAAAATAGCAC[A/G]CAGGAAATGTCAGTA | 81018 |
rs27274402 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf114 | Mm_Celera | 2:167509512 | TGTTCCCACATTTAA[A/G]TTGAGGCTCCTAAGT | 81018 |
rs27274403 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Rnf114 | Mm_Celera | 2:167509391 | TCTTGAATTCTCCTA[A/C]GTATCATAAGGTAGA | 81018 |
rs27274404 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf114 | Mm_Celera | 2:167509317 | TTTTTATTCTCTAGT[C/T]AGGGTCTCTGTGCCC | 81018 |
rs27274405 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf114 | Mm_Celera | 2:167508133 | CTGGGTCAGTTTGCT[A/G]AGTGGTGTTGCACAC | 81018 |
rs27274406 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Rnf114 | Mm_Celera | 2:167507962 | ACTTACACTGGGCTG[A/T]GTCACCGTGCCGTGT | 81018 |
rs27274407 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Rnf114 | Mm_Celera | 2:167507928 | AGTGTCTCTCTACCC[A/G]TGGAATGTGGCCTCC | 81018 |
rs27274408 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Rnf114 | Mm_Celera | 2:167507525 | AGCTAGGAGACCTAA[G/T]CCAGCCTGGGCTGCT | 81018 |
rs27274409 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf114 | Mm_Celera | 2:167507477 | TAACAGGCCACCTTC[C/T]GCTAATCTAAGCACT | 81018 |
rs27274410 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Rnf114 | Mm_Celera | 2:167507033 | ACACAGGTTCTCTGT[A/G]TGTCTTGTTCTAGCT | 81018 |
rs27274411 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf114 | Mm_Celera | 2:167506740 | CACAGTACATGGTCA[A/G]TCTCCAGCAGATGGG | 81018 |
rs27274412 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf114 | Mm_Celera | 2:167506654 | GCCCCACTGGGTTTG[C/T]GTGTTCCCACAATGC | 81018 |
rs27274413 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf114 | Mm_Celera | 2:167506614 | CCTCTGAGGTCTGAC[C/T]AGCACTGTTCTTGGG | 81018 |
rs27274414 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf114 | Mm_Celera | 2:167506551 | AGGGCATGGAATATT[C/T]TCTCCTTGTCTGTCA | 81018 |
rs27274415 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf114 | Mm_Celera | 2:167506235 | CATGGTGTTTGAGTT[C/T]CTTGAATATGTGAGA | 81018 |
rs27274416 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf114 | Mm_Celera | 2:167505719 | AGTGTCATCTCAGAG[A/G]AACTCCCTATGCTCC | 81018 |
rs27274417 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf114 | Mm_Celera | 2:167505538 | GCTTTAATCTGTATG[C/T]TGGCTTGGATTCCTC | 81018 |
rs27274418 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf114 | Mm_Celera | 2:167505321 | AGGTCAAGCCCTGTG[A/G]CTACACCCTTTCAGG | 81018 |
rs27274419 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Rnf114 | Mm_Celera | 2:167505193 | GTGAGGGTAGCTGAC[A/T]TCTCTGAGCCTCCTC | 81018 |
rs27274420 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Rnf114 | Mm_Celera | 2:167505140 | AAACATAACCAGCCT[C/T]CGTACTCAGCAGATT | 81018 |
rs27274421 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Rnf114, Spata2 | Mm_Celera | 2:167494011 | TAATACCAGCTCCCT[A/G]GTGAGATGTAGCCAG | 81018 |
rs27274422 | snp | C/T | 0.493827 | 0.0552116 | intron-variant, upstream-variant-2KB | Rnf114, Spata2 | Mm_Celera | 2:167493680 | GACGACCTCACTGTG[C/T]GGTTCTGTAATCCTA | 81018 |
rs27274423 | snp | C/T | 0.408163 | 0.193609 | utr-variant-5-prime, upstream-variant-2KB | Rnf114, Spata2 | Mm_Celera | 2:167493339 | TGTTACTGCTGGCTA[C/T]GGAGGTTAAGGATGC | 81018 |
rs29518722 | snp | G/T | 0.32 | 0.24 | intron-variant | Rnf114 | Mm_Celera | 2:167496446 | AGTTACATTGAGACC[G/T]GTCCCAGCCCCACCC | 81018 |
rs29518990 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf114 | Mm_Celera | 2:167504336 | GGTAGCCGTTACCGA[C/T]CGCCCGCCGCCACTA | 81018 |
rs29524890 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB, intron-variant | Rnf114, Spata2 | Mm_Celera | 2:167492035 | ACAATACAAGGGCCC[C/T]ACACCCCTACTAGCC | 81018 |
rs29528683 | snp | A/G | 0.5 | 0 | intron-variant | Rnf114 | Mm_Celera | 2:167498718 | ATTAATTATTGTGTT[A/G]GGGTGGGGAAGGGGG | 81018 |
rs29555574 | snp | C/T | 0.48 | 0.0979796 | intron-variant, upstream-variant-2KB | Rnf114, Spata2 | Mm_Celera | 2:167493560 | TAGATTCAGGCAACA[C/T]GCTCATATAGGTAAA | 81018 |
rs29555635 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rnf114 | Mm_Celera | 2:167496887 | CCGTGACCCCTGCCG[A/T]GGGCTTCCTTGGCTT | 81018 |
rs29559535 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf114 | Mm_Celera | 2:167498839 | ATCGCTGAGGTCAAG[C/T]ACCTAAGCCACCCAC | 81018 |
rs29574820 | snp | C/G | 0.375 | 0.216506 | upstream-variant-2KB, intron-variant | Rnf114, Spata2 | Mm_Celera | 2:167492068 | CAGAAACACTGCCAC[C/G]GGGGCCTTCCAAAGC | 81018 |
rs29620183 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf114 | Mm_Celera | 2:167508910 | CCAAGTGCTGAGATC[A/G]AAGGCCTGGGCCACA | 81018 |
rs29623175 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf114 | Mm_Celera | 2:167504980 | GAAATACTAATGACT[A/G]TTCAAACTATGGTGT | 81018 |
rs29671577 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf114 | Mm_Celera | 2:167500144 | CACACCAGAAGAGGG[C/T]ATCAGATCCCATTAC | 81018 |
rs29858331 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB, intron-variant | Rnf114, Spata2 | Mm_Celera | 2:167490919 | AGGCCCCAAGAACTG[A/G]CTTCCTCTCATTCAG | 81018 |
rs29907271 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf114 | Mm_Celera | 2:167508800 | CCAGGTTTGTTTGGG[A/G]TTTTTTGTTGTTTTG | 81018 |
rs32913831 | snp | A/G/T | 0.375 | 0.216506 | intron-variant | Rnf114 | GRCm38.p3 | 2:167497122 | TATCGAAAACCAACC[A/G/T]GAGACAGGAATGTGG | 81018 |
rs32916015 | snp | G/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Rnf114, Spata2 | Mm_Celera | 2:167494603 | AAGAGCACTGCCTGC[G/T]GTTCCAGAGGTCTTG | 81018 |
rs32971582 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Rnf114, Spata2 | Mm_Celera | 2:167494866 | AGTCCAGGCTACTCT[C/T]CGACTCGTGGAGCTC | 81018 |
rs33019218 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf114 | Mm_Celera | 2:167496882 | TTACCCCGTGACCCC[C/T]GCCGTGGGCTTCCTT | 81018 |
rs33041120 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf114 | Mm_Celera | 2:167511611 | GTCTTGTGTAGGCAA[A/G]GCTGGCCTCAGATTC | 81018 |
rs33093282 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rnf114 | Mm_Celera | 2:167495625 | CCCATCCCTGATACC[A/C]GGCTGTAGATGCCCT | 81018 |
rs33098755 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Rnf114, Spata2 | Mm_Celera | 2:167494810 | GTAGTCTAGGTCAGT[C/T]AAGAGCTTGGTGTTA | 81018 |
rs33143114 | snp | A/C/T | 0.375 | 0.216506 | intron-variant | Rnf114 | GRCm38.p3 | 2:167496978 | ATGGCAGACGGTGAG[A/C/T]GGTGTAGCCGCCAAG | 81018 |
rs33152380 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Rnf114, Spata2 | Mm_Celera | 2:167492171 | CCAAGTCCCCTCTCT[A/G]CAGGGAATGTAAACC | 81018 |
rs33159942 | snp | A/C | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Rnf114 | Mm_Celera | 2:167501402 | GAGGATCTGCCCCCC[A/C]CCCAACCCACCTCCA | 81018 |
rs33402805 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf114 | Mm_Celera | 2:167504872 | ACTTCAGTTCGCTCC[C/T]GAGGAGCCACATGGT | 81018 |
rs33411166 | snp | A/C | 0.5 | 0 | intron-variant | Rnf114 | GRCm38.p3 | 2:167498752 | TGTCACAGCACAGCA[A/C]AGCACAGGTGTGCAG | 81018 |
rs33416674 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf114 | Mm_Celera | 2:167500038 | CTCTCTTTCTTTCTT[C/T]CTTTCTTTCTTTCTT | 81018 |
rs33419372 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Rnf114, Spata2 | Mm_Celera | 2:167491900 | TCCCTGATCCAGCTT[C/T]AGTCTCCACACAGGA | 81018 |
rs33436334 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf114 | Mm_Celera | 2:167511016 | GAAAGACGTGGGATG[C/T]GTGTGTTGTTGGAGG | 81018 |
rs33481994 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB, intron-variant | Rnf114, Spata2 | Mm_Celera | 2:167491076 | CACAGGGCCAAGAAG[A/G]AGCGGATCTGAGACC | 81018 |
rs33594110 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf114 | Mm_Celera | 2:167499380 | AAGGCTGAGTACTCG[C/T]TATGCAGCACCATGC | 81018 |