SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs31133974 | snp | C/T | 0.375 | 0.216506 | intron-variant | Klhl25 | Mm_Celera | 7:75869406 | ATCCCAGTACATGTC[C/T]TCAAAATGGCAATGA | 207952 |
rs31142587 | snp | A/G | 0.375 | 0.216506 | intron-variant | Klhl25 | Mm_Celera | 7:75869455 | GCCTCCTGAGTTCTC[A/G]GGGGCCCCAGCAGTC | 207952 |
rs31307937 | snp | G/T | 0.375 | 0.216506 | intron-variant | Klhl25 | Mm_Celera | 7:75869068 | GCTGCTCTGCTTTGG[G/T]TTAGGCTCAGGACCT | 207952 |
rs31347478 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Klhl25 | Mm_Celera | 7:75860499 | TGTGATCTGAGTCTT[C/T]ATGAGTTTTCCATGG | 207952 |
rs31453189 | snp | C/T | 0.484429 | 0.0868505 | utr-variant-3-prime | Klhl25 | GRCm38.p3 | 7:75873411 | CCACCTGCCTTAGTC[C/T]TGTGTCCTGCCTGCT | 207952 |
rs31477782 | snp | C/T | 0.375 | 0.216506 | intron-variant | Klhl25 | Mm_Celera | 7:75860529 | GGGCTAGGTAGTTTA[C/T]CTGTGCCATGTGCCC | 207952 |
rs31577996 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Klhl25 | Mm_Celera | 7:75852807 | GTGTGTGTGTGTGTG[G/T]GGGGGGGGGAAACAA | 207952 |
rs31596103 | snp | C/T | 0.375 | 0.216506 | intron-variant | Klhl25 | Mm_Celera | 7:75860689 | ATTTGTGTATGTGTT[C/T]ATATATGCGGAGATC | 207952 |
rs31657244 | snp | C/T | 0.375 | 0.216506 | intron-variant | Klhl25 | Mm_Celera | 7:75858667 | TTTGCAAACCACTGT[C/T]AGGGTGAAGCTCCCT | 207952 |
rs31700973 | snp | C/T | 0.375 | 0.216506 | intron-variant | Klhl25 | Mm_Celera | 7:75869485 | CTGGCCACCCAGTAC[C/T]TCCTCCTCCATCTGG | 207952 |
rs31710675 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Klhl25 | GRCm38.p3 | 7:75856363 | GGGCAACTGTGTGGA[C/T]GTGAGGGTACGTGCG | 207952 |
rs31719390 | snp | C/T | 0.375 | 0.216506 | intron-variant | Klhl25 | Mm_Celera | 7:75859495 | CCTGAAGACCACAGT[C/T]CCATCCTTGGGACCC | 207952 |
rs31791233 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | Klhl25 | GRCm38.p3 | 7:75872746 | GACAGCTCCAGCCCC[A/G]GGCGGCAGCAGCTCA | 207952 |
rs31807722 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon | Klhl25 | Mm_Celera | 7:75865947 | CCTCATCTCCAGAGA[C/T]GAGCTGGAGACTGAG | 207952 |
rs31966688 | snp | C/G | 0.375 | 0.216506 | intron-variant | Klhl25 | GRCm38.p3 | 7:75859527 | CATGGTTTATGGAGA[C/G]ACCAGTATCTGCAAG | 207952 |
rs31979872 | snp | A/G | 0.375 | 0.216506 | intron-variant | Klhl25 | Mm_Celera | 7:75859379 | TGGAAATGCTGGGTG[A/G]GGCAAAGGGGACCTG | 207952 |
rs31996783 | snp | A/G | 0.444444 | 0.157135 | downstream-variant-500B | Klhl25 | GRCm38.p3 | 7:75874451 | CTACCACTCTGAACT[A/G]TAAACACAGGAGTAT | 207952 |
rs32021916 | snp | A/G | 0.32 | 0.24 | intron-variant | Klhl25 | Mm_Celera | 7:75870623 | TGGACAGAATTAGGG[A/G]CATAGACTAAGACCT | 207952 |
rs32111064 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Klhl25 | Mm_Celera | 7:75860588 | TATCTGTGGTTAATT[G/T]TACTTGTTCTTGCTG | 207952 |
rs32262760 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Klhl25 | Mm_Celera | 7:75855120 | GGGGCAAGGGAGTGC[A/G]GCACTCTCCCAAGCA | 207952 |
rs32298197 | snp | C/T | 0.375 | 0.216506 | synonymous-codon | Klhl25 | Mm_Celera | 7:75866028 | AGAGCAGAGGAAGGC[C/T]CACCTGCCCCTGCTC | 207952 |
rs32359320 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Klhl25 | Mm_Celera | 7:75869353 | GGAAGCAGGCACAGA[C/T]GGAGTCAACCTCAGA | 207952 |
rs32392143 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl25 | Mm_Celera | 7:75855213 | AGTAGTAGGCCGGGT[C/T]GCCAGGTTTCCTCTC | 207952 |
rs32402355 | snp | C/G | 0.375 | 0.216506 | intron-variant | Klhl25 | Mm_Celera | 7:75869682 | CCTCAGCCTCCATGG[C/G]CTGTGGGATGGGAGG | 207952 |
rs32505260 | snp | A/G | 0.375 | 0.216506 | intron-variant | Klhl25 | Mm_Celera | 7:75858466 | GTGGGGAGGAAGAAC[A/G]TGAAGAAGTGTGGGC | 207952 |
rs32514613 | snp | A/G | 0.48 | 0.0979796 | downstream-variant-500B | Klhl25 | GRCm38.p3 | 7:75874273 | AATTGTATTCAGTAG[A/G]CCAGGCTTGTGCACC | 207952 |
rs45725573 | snp | A/C | 0.231111 | 0.249285 | upstream-variant-2KB | Klhl25 | Mm_Celera | 7:75846484 | TAAATGTCTCCAGAT[A/C]TAGGCGGTATGGAGA | 207952 |
rs45727936 | snp | C/T | 0.489796 | 0.070696 | synonymous-codon | Klhl25 | Mm_Celera | 7:75865651 | GTGTTGGAGCTGCTG[C/T]TGGACTTTGCCTACT | 207952 |
rs45772053 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Klhl25 | Mm_Celera | 7:75849088 | TCCCATGCGTTGCCC[A/T]GGCGCGAGAATTCCG | 207952 |
rs45809501 | snp | A/G | 0.32 | 0.24 | intron-variant | Klhl25 | Mm_Celera | 7:75869722 | CCAGTATAGGAGAGG[A/G]CCAGGCACCTTAAAA | 207952 |
rs45823283 | snp | C/T | | | intron-variant | Klhl25 | Mm_Celera | 7:75862793 | TCCACCATGTGGTTG[C/T]TGGGAATTGAACTCA | 207952 |
rs45922571 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Klhl25 | Mm_Celera | 7:75854355 | CCCTGCCTAGCCCTG[C/T]TCCCTGGTTGCTGTC | 207952 |
rs45965581 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Klhl25 | Mm_Celera | 7:75872544 | AGGGAGCACAGTCTG[C/T]TGGGTGACAAATGGG | 207952 |
rs45997079 | snp | A/G | 0.5 | 0 | intron-variant | Klhl25 | GRCm38.p3 | 7:75869043 | CCTGGTCCTGCACAT[A/G]TCGTTAGGAGCTGCT | 207952 |
rs46039328 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl25 | Mm_Celera | 7:75851350 | TCTAAGTGACAGTAC[C/T]CTGGGCTGAGATGTG | 207952 |
rs46137630 | snp | G/T | 0.5 | 0 | intron-variant | Klhl25 | Mm_Celera | 7:75868482 | TCCTCCCAGAGGAAG[G/T]TAGCAGTGTCTAGGT | 207952 |
rs46212182 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl25 | Mm_Celera | 7:75863988 | GGAACTGACACAGGG[C/T]TCATCTTATTCTCAC | 207952 |
rs46225611 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Klhl25 | GRCm38.p3 | 7:75868311 | CAGCCTGCACCGGGA[A/T]GCAGTGCTCCTGAGC | 207952 |
rs46540336 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Klhl25 | Mm_Celera | 7:75858703 | GCCCCCAGATCAAAA[C/T]AGTTTTCCCAGTAAT | 207952 |
rs46564246 | snp | A/G | | | intron-variant | Klhl25 | Mm_Celera | 7:75862068 | CCTGCCAACATTTCT[A/G]TCTGCACTGCAGGCT | 207952 |
rs46681682 | snp | C/T | 0.32 | 0.24 | intron-variant | Klhl25 | Mm_Celera | 7:75855411 | GCCTAAAGCAGGGCA[C/T]ATTTGTTTGCGGACA | 207952 |
rs46729854 | snp | C/T | | | intron-variant | Klhl25 | Mm_Celera | 7:75865070 | GATTGACTTGTTTAA[C/T]GAGGGTGATCACAAA | 207952 |
rs46755511 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl25 | Mm_Celera | 7:75860399 | ACATGAAAATACAAA[C/T]CCTTCAAACACCTGA | 207952 |
rs46770871 | snp | A/C | | | intron-variant, utr-variant-5-prime | Klhl25 | Mm_Celera | 7:75862990 | GCCTCGAACTCACAG[A/C]CATCCACCTCCTTCA | 207952 |
rs46795299 | snp | A/G | 0.297521 | 0.245442 | downstream-variant-500B | Klhl25 | Mm_Celera | 7:75874156 | GGTTCTGATTCTGCC[A/G]TGGCTATGTTGAGTT | 207952 |
rs46829854 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Klhl25 | Mm_Celera | 7:75849949 | CCTTGCGCCATGCAG[C/T]GGTGCAGGATCCGTG | 207952 |
rs46859556 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Klhl25 | Mm_Celera | 7:75870707 | CACCAACCATTACAC[C/T]TGTAAGCATATGGAG | 207952 |
rs46862326 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Klhl25 | Mm_Celera | 7:75859238 | GTAGTACTACTTTAC[C/T]GCAGAGACCCATGCA | 207952 |
rs46887515 | snp | A/G | | | intron-variant | Klhl25 | Mm_Celera | 7:75858952 | CCCTGGTTATCCGAA[A/G]AGGCTGTATCTGGGT | 207952 |
rs46914166 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Klhl25 | Mm_Celera | 7:75861319 | CATGGAAATGCCAGG[A/G]TTCAGGGATATTGTT | 207952 |
rs46962929 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Klhl25 | Mm_Celera | 7:75851822 | TGAGTCTTTTTCCAT[C/T]CACACTGATCTGCCC | 207952 |
rs46988111 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime | Klhl25 | Mm_Celera | 7:75873727 | ACCAGGCTCATCCCT[C/T]GTTTGTCTAGTGCTC | 207952 |
rs47133396 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl25 | Mm_Celera | 7:75852337 | ATAACTGCTCCTCAG[C/T]GGGGCTGCTCTGTGA | 207952 |
rs47154863 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl25 | Mm_Celera | 7:75848933 | AGCATAGGGTCCTTC[C/T]TGTCTGGAAAGTTGT | 207952 |
rs47164103 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Klhl25 | Mm_Celera | 7:75859405 | ACCTGGTTGATCTCC[C/T]AAGAGGTGGTGCTGG | 207952 |
rs47235053 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Klhl25 | Mm_Celera | 7:75869972 | CCCCCTGGGCCTGGT[C/T]TTTTTAGATCTACTA | 207952 |
rs47267272 | snp | A/T | 0.32 | 0.24 | intron-variant | Klhl25 | Mm_Celera | 7:75870392 | ATCTTGGTGGTGTCC[A/T]TCATGCAATGATCAC | 207952 |
rs47269595 | snp | C/T | 0.375 | 0.216506 | intron-variant | Klhl25 | Mm_Celera | 7:75858554 | TGATACTGACTCCAG[C/T]CCCATCTTGGGTGTG | 207952 |
rs47272205 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Klhl25 | Mm_Celera | 7:75870852 | CGAACTCACATCCCC[C/T]GCTTGCATCCTCAAT | 207952 |
rs47330207 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl25 | Mm_Celera | 7:75852123 | AGGAGGAGTTGGAGA[A/G]TCAGCCTGTGATAGG | 207952 |
rs47353278 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Klhl25 | Mm_Celera | 7:75851795 | TGTACTTTCCAGGAA[C/T]TCATAAAATCCTGAG | 207952 |
rs47355878 | snp | C/G | | | intron-variant | Klhl25 | Mm_Celera | 7:75859063 | AGTCAGCGCTGTGGA[C/G]AAAGTTTCAAATTGA | 207952 |
rs47382047 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl25 | Mm_Celera | 7:75858268 | AGACCAGGAAATGTC[A/G]GCTGTGAGGCCCAAA | 207952 |
rs47400724 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl25 | Mm_Celera | 7:75865132 | GGACTGGAAATATGT[C/T]CTTGCTGAGCATCAC | 207952 |
rs47404902 | snp | C/T | | | intron-variant | Klhl25 | Mm_Celera | 7:75862376 | TCTGAGGGGCGTTGG[C/T]TGACACAGTGTATCC | 207952 |
rs47410800 | snp | A/C | | | intron-variant | Klhl25 | Mm_Celera | 7:75862324 | GTCAGTAAGATGACG[A/C]TTACCACAAGTGTGT | 207952 |
rs47411094 | snp | C/G | 0.5 | 0 | intron-variant | Klhl25 | Mm_Celera | 7:75868414 | TCTAAGCACGAGCAG[C/G]TGGCTCCTGAGCAGT | 207952 |
rs47413385 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl25 | Mm_Celera | 7:75854933 | CAACCTGATCTTTAG[A/G]AACAGACATTAGACA | 207952 |
rs47413823 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Klhl25 | Mm_Celera | 7:75874124 | AATAAAAGTGCGGAC[A/G]TTCTTGATCTCCTTT | 207952 |
rs47423264 | snp | C/T | 0.32 | 0.24 | utr-variant-5-prime, upstream-variant-2KB | Klhl25 | Mm_Celera | 7:75848379 | AGTTTGTTGGCAGCG[C/T]CCGTGCGGTTCGGCT | 207952 |
rs47565963 | snp | C/G | | | intron-variant | Klhl25 | Mm_Celera | 7:75861130 | GGTTCTGATCTGCCC[C/G]GTGGATACCTGGCAG | 207952 |
rs47608285 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Klhl25 | Mm_Celera | 7:75861405 | GAGCTCCTGAGTGTG[C/G]GTGTTGCTCTAGGCA | 207952 |
rs47610940 | snp | A/G | | | intron-variant | Klhl25 | Mm_Celera | 7:75859337 | GGATGCTCCTGTCTG[A/G]GTGAACTGAAGGAAG | 207952 |
rs47642379 | snp | A/G | | | intron-variant | Klhl25 | Mm_Celera | 7:75863424 | GAGTGCATAGGGTTG[A/G]GGTAGAGCTGGGTGT | 207952 |
rs47669481 | snp | A/T | | | intron-variant | Klhl25 | Mm_Celera | 7:75863134 | ACCAGGACTCCCTGC[A/T]GGGTCCTTTGTAATA | 207952 |
rs47679853 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Klhl25 | Mm_Celera | 7:75872679 | GGCTTTCATCGTCTC[C/T]CTCTGCTTTATCCCA | 207952 |
rs47688018 | snp | A/C | 0.21875 | 0.248039 | missense | Klhl25 | Mm_Celera | 7:75865509 | ACTCTGGGCTGGTGA[A/C]CGAGCCTTTCCTTGC | 207952 |
rs47694954 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl25 | Mm_Celera | 7:75870796 | CCTGTCTTGCAAAGC[C/T]GGTGGAACACACACA | 207952 |
rs47705451 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Klhl25 | Mm_Celera | 7:75869551 | AGTGTTCCTGTTCTC[C/T]GAAGGCTCCTCTCGT | 207952 |
rs47822819 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Klhl25 | Mm_Celera | 7:75872673 | AGTGTGGGCTTTCAT[C/T]GTCTCCCTCTGCTTT | 207952 |
rs47845600 | snp | C/G | | | intron-variant | Klhl25 | Mm_Celera | 7:75863694 | CATGCCTAGGAGAGG[C/G]TAGCACAGCACAGCT | 207952 |
rs47892212 | snp | C/T | 0.32 | 0.24 | intron-variant | Klhl25 | Mm_Celera | 7:75857025 | GCCGGGCTCTTGACA[C/T]GCTCCAGTTTAATTA | 207952 |
rs47908756 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Klhl25 | Mm_Celera | 7:75863880 | TCTGTGCATTACCAA[A/G]CCCTGCTTCTCCGTT | 207952 |
rs47957052 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Klhl25 | Mm_Celera | 7:75854798 | GCCAGGCTCCTCCAG[A/T]CCTTCCCTGGTGTCT | 207952 |
rs47993916 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Klhl25 | Mm_Celera | 7:75861465 | CTTGAATGAGTATGT[C/T]TGGGCATGTGGATCC | 207952 |
rs48017000 | snp | C/T | 0.142012 | 0.225474 | utr-variant-3-prime | Klhl25 | Mm_Celera | 7:75872840 | AAGCTGGCAGCGGCT[C/T]GTGTGGAGAGAAGCG | 207952 |
rs48019210 | snp | A/C | | | intron-variant | Klhl25 | Mm_Celera | 7:75863953 | TGCAGGCAGGGCAAG[A/C]GGTGTGAGCCCTGAG | 207952 |
rs48063404 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl25 | Mm_Celera | 7:75852432 | CAGGCAGATGACTCA[C/T]TCCCAAGGTTTCCCT | 207952 |
rs48085718 | snp | G/T | | | intron-variant | Klhl25 | Mm_Celera | 7:75862487 | TGGGGGTGGGGAGTG[G/T]AGAGAAAGCCAGTGT | 207952 |
rs48102005 | snp | A/G | | | intron-variant | Klhl25 | Mm_Celera | 7:75864688 | AGAGGCCATCAGAGG[A/G]TTGTGAGCTGCCACA | 207952 |
rs48143115 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Klhl25 | Mm_Celera | 7:75859874 | GCCAGATTGCTGGAG[A/T]GGCAGCCTCTTTCTG | 207952 |
rs48248100 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Klhl25 | Mm_Celera | 7:75871400 | GTGTTTCTTTTCCTG[A/T]CACAGGCATTCCTTT | 207952 |
rs48308521 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Klhl25 | Mm_Celera | 7:75868553 | TAATTGTCTATTCCT[A/G]TCATTGGTGACCTGA | 207952 |
rs48340951 | snp | A/G | 0.32 | 0.24 | intron-variant | Klhl25 | Mm_Celera | 7:75870651 | CCTTGACGTGGAGTC[A/G]TTCACCTGGAGCCCT | 207952 |
rs48388587 | snp | C/T | | | intron-variant | Klhl25 | Mm_Celera | 7:75862308 | GTGACCCAAAAGTGG[C/T]GTCAGTAAGATGACG | 207952 |
rs48412913 | snp | A/G | 0.5 | 0 | intron-variant | Klhl25 | Mm_Celera | 7:75868277 | CTGGCGAGCATCCTC[A/G]GCCTGTGAACCTGTG | 207952 |
rs48416499 | snp | C/T | 0.32 | 0.24 | intron-variant | Klhl25 | Mm_Celera | 7:75871095 | CTGGGCATGACAGAC[C/T]CCCTGTGGATCAGTA | 207952 |
rs48453693 | snp | C/G | | | intron-variant | Klhl25 | Mm_Celera | 7:75859939 | AGAGTGTCTGGTGTT[C/G]TGTGTAGGGCGGTGC | 207952 |
rs48502451 | snp | C/T | | | intron-variant | Klhl25 | Mm_Celera | 7:75858118 | AGAGAACGGGTTGAA[C/T]AAGACTTGAACATCC | 207952 |
rs48531470 | snp | C/T | 0.244898 | 0.249948 | utr-variant-3-prime | Klhl25 | Mm_Celera | 7:75872894 | GCAACCAACGACATT[C/T]GTGCAGAGCCTTGAG | 207952 |