SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6378221 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Klhl6 | Mm_Celera | 16:19983904 | CAAGACATAGGCTTA[C/T]GGCATGACATTTCAG | 239743 |
rs6378761 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Klhl6 | Mm_Celera | 16:19983999 | ATGAGCCTCTTCATG[A/G]CAACTTATNCCATAC | 239743 |
rs6378777 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Klhl6 | Mm_Celera | 16:19984008 | TTCATGNCAACTTAT[A/G]CCATACTCTCTCAAA | 239743 |
rs45650491 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Klhl6 | Mm_Celera | 16:19958708 | AAAAAGTAGCTGTGT[A/G]CTGTGGGCAAAGAAG | 239743 |
rs45748113 | snp | C/T | 0.132653 | 0.220748 | synonymous-codon | Klhl6 | Mm_Celera | 16:19956964 | GAAGACTTCAGGGCA[C/T]TGTCTAATAAGAGGG | 239743 |
rs45789717 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Klhl6 | Mm_Celera | 16:19953426 | CTTTCTACTAGGGAA[C/G]TGCTTTAGTGCTAGC | 239743 |
rs45799720 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Klhl6 | Mm_Celera | 16:19955870 | GTCCTAGTTCCTACT[A/G]TAACAAGTTGCAAGT | 239743 |
rs45877846 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Klhl6 | Mm_Celera | 16:19954041 | CCTTGTCTGAAACCT[A/G]AACTCCTGGAATGAA | 239743 |
rs45881295 | snp | A/G | | | intron-variant | Klhl6 | Mm_Celera | 16:19966833 | ACTCATTCACATCAT[A/G]GCATAATGAGAATGC | 239743 |
rs45913579 | snp | C/T | 0.142012 | 0.225474 | downstream-variant-500B | Klhl6 | Mm_Celera | 16:19946266 | ACCCCAGCCAGTAAA[C/T]GGCAGTGAGAGTTCT | 239743 |
rs45943555 | snp | C/T | 0.132653 | 0.220748 | utr-variant-3-prime | Klhl6 | Mm_Celera | 16:19946530 | TTCCCTTATCTTTAG[C/T]AAACTTGCCAGACAG | 239743 |
rs45999965 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Klhl6 | Mm_Celera | 16:19972741 | TGCCTTGGCCTCTTA[C/T]GTCTCTAGCTAACAG | 239743 |
rs46015101 | snp | A/G | 0.244898 | 0.249948 | synonymous-codon | Klhl6 | Mm_Celera | 16:19953631 | TGTACAGCCGCCAAT[A/G]ATCATGAACACCTCA | 239743 |
rs46047970 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Klhl6 | Mm_Celera | 16:19972939 | GGTTTTATTCCCCAA[A/G]GGTTTGTGTGTTCTA | 239743 |
rs46204361 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Klhl6 | GRCm38.p3 | 16:19978427 | TACATTGACACTCTT[C/T]TCATCTCTCCTGTTT | 239743 |
rs46253571 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Klhl6 | Mm_Celera | 16:19975777 | ATCATTTGAGTCCAT[C/T]GCTCCATACCTGTGA | 239743 |
rs46260478 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl6 | Mm_Celera | 16:19949773 | GCTAGTGGGAGATAA[A/G]GTCTGATAGGAGGGA | 239743 |
rs46364290 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Klhl6 | Mm_Celera | 16:19971813 | GGATCAATCATAATT[C/T]AAGCTCCAAGATCAG | 239743 |
rs46370319 | snp | C/G | 0.260355 | 0.249785 | utr-variant-3-prime | Klhl6 | Mm_Celera | 16:19946585 | GCTTCCTGTTTTCCT[C/G]TCTGAATTAGGCAGT | 239743 |
rs46452162 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Klhl6 | Mm_Celera | 16:19949498 | CTCCACATTGTTGAT[C/T]CTTTGTAAGCCATCA | 239743 |
rs46548833 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Klhl6 | Mm_Celera | 16:19949310 | GGTGTTATTACTGGA[A/T]CTAGATTAGTAACGT | 239743 |
rs46574316 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Klhl6 | Mm_Celera | 16:19952204 | GATGGAACACACTAA[A/C]CCCACATCTATTCTG | 239743 |
rs46584726 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Klhl6 | Mm_Celera | 16:19948334 | AGAAGTCAATGTGCT[A/G]CTCAGATTGCTGGAA | 239743 |
rs46659337 | snp | A/G | 0.142012 | 0.225474 | utr-variant-3-prime | Klhl6 | Mm_Celera | 16:19946987 | TCAGAGACTCCAGGG[A/G]TAGTCACACAGACAC | 239743 |
rs46679599 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl6 | Mm_Celera | 16:19948977 | GGTTTCCTTGTCCTG[A/G]GGTAGTTTTTAACCA | 239743 |
rs46688616 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Klhl6 | Mm_Celera | 16:19974029 | GTGGATCCAAGCAAA[A/G]CCAGTTTCAGAAACT | 239743 |
rs46689027 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Klhl6 | Mm_Celera | 16:19956462 | AAGGTCAGACCAGGG[G/T]TGAAGTTGACACCTG | 239743 |
rs46694607 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Klhl6 | Mm_Celera | 16:19976874 | GATGTCAATGTGAAC[A/C]CAGCAGTTTCTTAAA | 239743 |
rs46698288 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Klhl6 | Mm_Celera | 16:19976392 | GCATCCACAGTTTGA[C/G]AGAAATCATTAAACT | 239743 |
rs46786982 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Klhl6 | Mm_Celera | 16:19973805 | CTCCGGTGATGATCC[A/G]GACACAGATCTGATG | 239743 |
rs46818740 | snp | A/T | 0.142012 | 0.225474 | utr-variant-5-prime | Klhl6 | Mm_Celera | 16:19983025 | CTAGACTAAAGGAGC[A/T]GCCAAGTTTCGGGGA | 239743 |
rs46819777 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl6 | Mm_Celera | 16:19957492 | AAAAATAATACATTC[C/T]CATAGCCAACAACTC | 239743 |
rs46850847 | snp | C/T | 0.124444 | 0.216185 | downstream-variant-500B | Klhl6 | Mm_Celera | 16:19946418 | GATCTTAGGAAATGC[C/T]CTTGACACACAGTGG | 239743 |
rs46904058 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Klhl6 | Mm_Celera | 16:19976999 | TCGTTATTTAATCAC[A/C]TATCTAGATCTGGAG | 239743 |
rs46935083 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Klhl6 | Mm_Celera | 16:19954551 | GGGAGCCCTGCAGGA[A/G]ACAGCAAGCCTTCAG | 239743 |
rs46944886 | snp | A/G/T | 0.152778 | 0.230321 | intron-variant | Klhl6 | GRCm38.p3 | 16:19975448 | TTTGGCGCTGAATGT[A/G/T]GACTTCTTTAGTACA | 239743 |
rs47052210 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Klhl6 | Mm_Celera | 16:19952877 | GTACAGATTTACCTA[C/G]TATAAAGTAACAATG | 239743 |
rs47060702 | snp | A/C/T | 0.244898 | 0.249948 | intron-variant | Klhl6 | Mm_Celera | 16:19981954 | TCCCACCACTCCTTG[A/C/T]ACACCAGAAACCCCT | 239743 |
rs47086479 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Klhl6 | Mm_Celera | 16:19976500 | ACATGTGGTACAAGC[A/T]CAATGACTTTTTAAC | 239743 |
rs47089565 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Klhl6 | Mm_Celera | 16:19949872 | GATGAGCAGTACTCA[C/T]ACCACTCAAGATGGA | 239743 |
rs47095674 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Klhl6 | Mm_Celera | 16:19980685 | TTACTGCCATACTGG[C/T]CTTGAGGACCAACAG | 239743 |
rs47098953 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Klhl6 | Mm_Celera | 16:19975359 | GATGAGGAAGAGAGG[A/G]AGTTATGCAGGCTCT | 239743 |
rs47116044 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Klhl6 | Mm_Celera | 16:19956607 | TAGGCAATGTCAGAA[A/T]AGAATAACAGATGCA | 239743 |
rs47173378 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Klhl6 | Mm_Celera | 16:19973781 | AACATAACAAATACT[C/G]TATACAGACTCCGGT | 239743 |
rs47249152 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Klhl6 | Mm_Celera | 16:19971348 | TCATCTTAGTCCAAA[A/T]TCTAGTCTCTAGTTA | 239743 |
rs47280729 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl6 | Mm_Celera | 16:19981203 | TGTCACCTCTATCAT[A/G]CCAGTGCAAAGCGAA | 239743 |
rs47308350 | snp | C/G | | | intron-variant | Klhl6 | Mm_Celera | 16:19967213 | AGGAAGTGAAGCTGG[C/G]CAGTAAGTAAGGAGG | 239743 |
rs47320851 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Klhl6 | Mm_Celera | 16:19949896 | AGATGGAGAGCAAAC[A/C]GAGAGGATCCAGGAA | 239743 |
rs47388253 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl6 | GRCm38.p3 | 16:19978071 | CTACACTGTAACTTG[C/T]TGCAACTTCTAGAGG | 239743 |
rs47401539 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Klhl6 | Mm_Celera | 16:19957551 | ATTACCTTAAGTCAT[A/G]TGAAAATGTGGAGAT | 239743 |
rs47426555 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl6 | Mm_Celera | 16:19952627 | ATGAACAGACCTAAA[A/G]AATAGCTGATAATAA | 239743 |
rs47457246 | snp | A/G | 0.244898 | 0.249948 | synonymous-codon | Klhl6 | GRCm38.p3 | 16:19956988 | AAGAGGGTCTGCTTC[A/G]ACCATCTCCACGAAG | 239743 |
rs47496768 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Klhl6 | Mm_Celera | 16:19955211 | GTCCAGTCTCTCTAA[A/C]CAAATATTTATGGTA | 239743 |
rs47504023 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Klhl6 | Mm_Celera | 16:19959476 | CCTGACAGGTGGAGC[A/G]CAGTATGCAAAGTAC | 239743 |
rs47532150 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Klhl6 | Mm_Celera | 16:19952183 | AAAGCTTTCTGTGCT[C/G]TGAGTGATGGAACAC | 239743 |
rs47551142 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl6 | Mm_Celera | 16:19953321 | GAGCTCCTGGTTCCA[C/T]ATTCCGACCGAGACA | 239743 |
rs47694264 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl6 | Mm_Celera | 16:19948559 | ATATACATGAAGTCA[A/G]CATATTCATATTCAT | 239743 |
rs47731669 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Klhl6 | Mm_Celera | 16:19980726 | GCACTGGCAAGGACA[G/T]ATCTGAACTAAAGCA | 239743 |
rs47802560 | snp | A/C | 0.277778 | 0.248452 | upstream-variant-2KB | Klhl6 | Mm_Celera | 16:19983340 | AGTTATTATCTGTTT[A/C]CTTATACCTGCATCA | 239743 |
rs47821790 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Klhl6 | Mm_Celera | 16:19976265 | GTTCTTCTGTCCCTT[C/T]TGCCAACACCTAGAA | 239743 |
rs47867068 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl6 | Mm_Celera | 16:19952912 | AGACTGTGTCATTCA[A/G]AAATATTTATTGAGC | 239743 |
rs47962356 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Klhl6 | Mm_Celera | 16:19973368 | GCATTTGAAAGTTCA[C/T]AGACATCTTTCTTTC | 239743 |
rs48081530 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Klhl6 | Mm_Celera | 16:19953789 | GGCCACAGTTTCCAC[G/T]CCACCATCGTTGGCC | 239743 |
rs48110831 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Klhl6 | Mm_Celera | 16:19975577 | CACAGGATACTGAAT[A/G]TAATAGCTATAGTAC | 239743 |
rs48118570 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Klhl6 | Mm_Celera | 16:19956710 | AACTGGGCAGAGGAC[A/G]GATGTGACAGGCACA | 239743 |
rs48145027 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Klhl6 | Mm_Celera | 16:19952138 | AGAGCACTTAGGGAA[C/G]CTAAAAGACAATCCT | 239743 |
rs48155020 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Klhl6 | Mm_Celera | 16:19955996 | TTCTTTGGAGAAGGC[A/G]ACCTTAGCTTGAATT | 239743 |
rs48169845 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Klhl6 | Mm_Celera | 16:19947810 | CTTTTTCACTGAATG[C/T]TTCTGTTTCCATATA | 239743 |
rs48181067 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB | Klhl6 | Mm_Celera | 16:19984168 | ACATGCCTTAAAAAC[C/T]ACTAATGAGGCCATC | 239743 |
rs48204762 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Klhl6 | Mm_Celera | 16:19953157 | ATCAGTGCCCTGAGC[C/T]TGTAGCAGACTGAAC | 239743 |
rs48217419 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Klhl6 | GRCm38.p3 | 16:19978113 | GTGGCTCTCCCTACT[C/T]ACAACCTAACAGGGC | 239743 |
rs48278432 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Klhl6 | Mm_Celera | 16:19952117 | TTTGTGTTTTCCATT[A/C]TTTTAAGAGCACTTA | 239743 |
rs48308885 | snp | A/G | | | intron-variant | Klhl6 | Mm_Celera | 16:19967443 | TCAGGGTTTCTGCAC[A/G]TTGTCCACCTTTATC | 239743 |
rs48346748 | snp | C/G | 0.244898 | 0.249948 | synonymous-codon | Klhl6 | Mm_Celera | 16:19957039 | TAAACGCACATTCTC[C/G]AGGACACAAGGGAGC | 239743 |
rs48427773 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl6 | Mm_Celera | 16:19959416 | CAGGGTAGGACAGGA[A/G]AGAAAGCCCATCTGA | 239743 |
rs48454377 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Klhl6 | Mm_Celera | 16:19976581 | ACTTCTGGTAGTTTT[C/T]CTGTAAATTTATAGC | 239743 |
rs48470988 | snp | A/C | 0.132653 | 0.220748 | utr-variant-3-prime | Klhl6 | Mm_Celera | 16:19946543 | AGCAAACTTGCCAGA[A/C]AGAGACACCAGCCGA | 239743 |
rs48564966 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Klhl6 | Mm_Celera | 16:19972550 | AAATAACTGGCTAGG[A/G]CTAGGACAAATATTC | 239743 |
rs48571813 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Klhl6 | Mm_Celera | 16:19958893 | TCTCCCACTGACTTT[C/T]ACAGGACTCTTCATT | 239743 |
rs48595578 | snp | C/T | 0.244898 | 0.249948 | synonymous-codon | Klhl6 | Mm_Celera | 16:19957120 | AAACACCTGAGCCTC[C/T]TCAGTCACACACAGG | 239743 |
rs48673571 | snp | C/T | 0.142012 | 0.225474 | downstream-variant-500B | Klhl6 | Mm_Celera | 16:19946446 | TGGCCTGAAAAACTC[C/T]AAGACCAGAGTTCTC | 239743 |
rs48772939 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Klhl6 | Mm_Celera | 16:19955699 | TTCACTAAACCCTGC[C/T]GTGTCTTTATAAGAT | 239743 |
rs48773198 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl6 | Mm_Celera | 16:19959165 | GAGAATATGAGCTTA[A/G]TGTTTGGATAGCATT | 239743 |
rs48960332 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Klhl6 | Mm_Celera | 16:19946876 | GGTCTCACATATCCC[A/G]ATCTTTGTCTTCCTA | 239743 |
rs48985447 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Klhl6 | Mm_Celera | 16:19953119 | TGTGGAAAGATAAAA[C/G]ATTTCTCTAGTACTA | 239743 |
rs49003515 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Klhl6 | Mm_Celera | 16:19971812 | TGGATCAATCATAAT[G/T]TAAGCTCCAAGATCA | 239743 |
rs49050676 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Klhl6 | Mm_Celera | 16:19955326 | TTGAAAAGAAACAGA[C/T]ACTACCAGCATTAAC | 239743 |
rs49067848 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Klhl6 | Mm_Celera | 16:19959397 | GGAAAGAAAAAGGAG[A/G]TCACAGGGTAGGACA | 239743 |
rs49119621 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Klhl6 | Mm_Celera | 16:19974972 | GCATCCAATACCATA[A/T]TCTTGCTCTTCTTAC | 239743 |
rs49149313 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Klhl6 | Mm_Celera | 16:19974382 | AGATTAAACTATTCC[A/T]CTCCACACTCTGACC | 239743 |
rs49251927 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Klhl6 | Mm_Celera | 16:19955459 | TGACAGGTCTAAGAA[A/C]AACTAAAAAGTAGAG | 239743 |
rs49273200 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Klhl6 | Mm_Celera | 16:19976436 | GTATAGAATGACAGG[A/G]AAAATGCTTACACTA | 239743 |
rs49288266 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Klhl6 | GRCm38.p3 | 16:19979795 | TTATTTGCATTCTAT[A/G]ACAACTCACTTTCAA | 239743 |
rs49382596 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Klhl6 | Mm_Celera | 16:19949179 | GGAGACAGACTCAGC[A/C]AGGATATGCCACCAA | 239743 |
rs49398278 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Klhl6 | Mm_Celera | 16:19948982 | CCTTGTCCTGGGGTA[A/G]TTTTTAACCAGCAGT | 239743 |
rs49400776 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Klhl6 | GRCm38.p3 | 16:19982365 | GAATCAGACCAAGGA[G/T]GAGATGAAAGGTTCC | 239743 |
rs49418662 | snp | C/G | | | intron-variant | Klhl6 | Mm_Celera | 16:19967247 | GCTCCCAGATACCCA[C/G]TTCCTCCAACTAGGT | 239743 |
rs49423658 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Klhl6 | Mm_Celera | 16:19955949 | GGTTTCATGACCAAA[G/T]ATTGAACCAATGACC | 239743 |
rs49443124 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Klhl6 | Mm_Celera | 16:19953979 | TTGTTGCTATTTTAA[A/G]ACAAGAGTTTATTTG | 239743 |
rs49550117 | snp | C/T | 0.32 | 0.24 | intron-variant | Klhl6 | Mm_Celera | 16:19975625 | AACGTTGCAATACAG[C/T]TTTCAGGGTTACTGA | 239743 |