SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6159183 | snp | A/C | 0.5 | 0 | intron-variant | Dcaf6 | Mm_Celera | 1:165341347 | TACTCTTACCAGCCA[A/C]CGGTGTGCTGGAGTT | 74106 |
rs6222458 | snp | A/C | 0.5 | 0 | upstream-variant-2KB | Mpc2, Dcaf6 | Mm_Celera | 1:165460803 | gaggctggaccatag[A/C]gagatccaagccagc | 74106 |
rs6290164 | snp | C/G | 0.5 | 0 | intron-variant | Dcaf6 | GRCm38.p3 | 1:165393907 | agagagagagagaga[C/G]aagagaaagngagac | 74106 |
rs6290191 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dcaf6 | Mm_Celera | 1:165393917 | AGAGACAAGAGAAAG[A/G]GAGACAGACAGACAG | 74106 |
rs6291204 | snp | A/G | 0.45995 | 0.135724 | intron-variant | Dcaf6 | Mm_Celera | 1:165394046 | TGATACATAGACGCA[A/G]TGAGATACAGTTCAT | 74106 |
rs6291719 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Dcaf6 | Mm_Celera | 1:165394162 | AAAACCTGCATGTTA[C/T]GCCGCATATGTGAAC | 74106 |
rs6292207 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Dcaf6 | Mm_Celera | 1:165394231 | TTGTATACACACATG[A/G]AAATGTAGCTAAAGT | 74106 |
rs6292256 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165394263 | CAAAAATGTAGAAAG[A/G]AGAANAAGAAAGGGT | 74106 |
rs6292277 | snp | C/G | 0.304688 | 0.243945 | intron-variant | Dcaf6 | Mm_Celera | 1:165394268 | ATGTAGAAAGNAGAA[C/G]AAGAAAGGGTTATAT | 74106 |
rs6293328 | snp | A/G | 0.5 | 0 | intron-variant | Dcaf6 | Mm_Celera | 1:165394439 | CATTTATTTGGCAGT[A/G]ATTGTGAACAGTTTT | 74106 |
rs6293451 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Dcaf6 | Mm_Celera | 1:165394509 | ATGTGACTAGTCTTA[C/T]TGACCCACTTGAAAG | 74106 |
rs6294525 | snp | C/T | 0.32 | 0.24 | intron-variant | Dcaf6 | Mm_Celera | 1:165394675 | CTGTCAGCCGCGCTC[C/T]GAGCCCAGTGNTCCC | 74106 |
rs6294547 | snp | C/T | 0.32 | 0.24 | intron-variant | Dcaf6 | Mm_Celera | 1:165394686 | GCTCNGAGCCCAGTG[C/T]TCCCTTGTGCTTCCT | 74106 |
rs6305837 | snp | A/C/T | 0.42 | 0.183303 | intron-variant | Dcaf6 | GRCm38.p3 | 1:165444036 | TCAGTGGAATGAATT[A/C/T]AAAAACTTCATTTTT | 74106 |
rs6305874 | snp | A/G | 0.5 | 0 | intron-variant | Dcaf6 | Mm_Celera | 1:165444066 | TAACTTTACTGTTGT[A/G]TGTGATGTGTGGGGG | 74106 |
rs6402658 | snp | A/T | 0.32 | 0.24 | intron-variant | Dcaf6 | Mm_Celera | 1:165443867 | TACAATCATTCTAGT[A/T]TAAGAACTAAGTAGG | 74106 |
rs13462739 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB | Mpc2, Dcaf6 | Mm_Celera | 1:165461334 | GACGAGCCGCCCTTC[A/C]GTTGTCAGCCAGGAA | 74106 |
rs13468336 | snp | A/G | 0.375 | 0.216506 | synonymous-codon, nc-transcript-variant | Dcaf6 | Mm_Celera | 1:165388731 | CCCTCGTTCCAGCTC[A/G]TTGCTGTCTTGCCCA | 74106 |
rs30467499 | snp | A/T | 0.32 | 0.24 | intron-variant | Dcaf6 | Mm_Celera | 1:165341608 | CTGTCTCAAAAAAAT[A/T]AAAAAAATCTTGTGG | 74106 |
rs30467676 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165401940 | ACCTGCAGCACCTGA[A/G]GCACAGCACAGTGGA | 74106 |
rs30473518 | snp | C/G | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165345247 | CCGTCTAAGCGAAAA[C/G]AGAGGTGCTCTCATT | 74106 |
rs30500832 | snp | A/C | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165425328 | GCTATCCCTTGCCCA[A/C]ACTTTTCTGATCTAA | 74106 |
rs30515034 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Dcaf6 | Mm_Celera | 1:165432311 | GAATCTGGACACAAA[C/G]TGATGGTGTTGTCTA | 74106 |
rs30515565 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Dcaf6 | Mm_Celera | 1:165368668 | TTTCCCCAAACCTGC[C/T]ACTTCTGGTCCCAAC | 74106 |
rs30521222 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dcaf6 | Mm_Celera | 1:165388038 | GTAAATAGTATATTC[C/T]ATAGTTGGGGTGGGA | 74106 |
rs30545976 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165354530 | AGAGTACTGTTATAG[C/T]TAACAACTACGAAGT | 74106 |
rs30546301 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165361234 | TGAGTTCCAGGATAG[C/T]CAGGGCTATACAGAG | 74106 |
rs30555667 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165436357 | TAAAGGAGCCAATCA[C/T]TGGGAAAAAATAAAC | 74106 |
rs30563883 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Dcaf6 | Mm_Celera | 1:165429940 | AAACCAGCCTGAATG[G/T]CCATTAAGAGCAAGA | 74106 |
rs30610540 | snp | A/C | 0.387812 | 0.208586 | intron-variant | Dcaf6 | Mm_Celera | 1:165368074 | AAATACCTTTAAGGA[A/C]ACATGTAACTTTAAG | 74106 |
rs30613671 | snp | A/C | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165401391 | TGCAATGTAAAATAT[A/C]ATTTTCTATGGCAAA | 74106 |
rs30617627 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165436307 | GTGTTGTGGATGGGC[C/T]TGGTGCTGTTCATGT | 74106 |
rs30645135 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165436866 | CCCCTGCTTTCTGAC[A/G]GTGGATACAGCATAC | 74106 |
rs30657582 | snp | A/C | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165412886 | GATTTACTGTTCTCT[A/C]CATACTATATGCCAG | 74106 |
rs30670662 | snp | A/C | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165361286 | CAACAACAACAACAA[A/C]AAAACAACAACAAAA | 74106 |
rs30699687 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165430528 | TATAGGTGTTACCTA[A/G]GAAGGATTTGTTCTG | 74106 |
rs30718241 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Dcaf6 | Mm_Celera | 1:165388931 | CTTCAAAAAAGCACA[C/T]GTTAAAGCAAACCCA | 74106 |
rs30747505 | snp | C/T | 0.32 | 0.24 | intron-variant | Dcaf6 | Mm_Celera | 1:165395125 | GGTCTCCATGGTCAG[C/T]CTGCTTCCTTATACA | 74106 |
rs30747953 | snp | C/G | 0.33241 | 0.236027 | downstream-variant-500B | Dcaf6 | Mm_Celera | 1:165329445 | AGCCCTCTTTTGTTA[C/G]AGAAATGACTAGAAA | 74106 |
rs30750950 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165451903 | TAAATACAGGTTTAA[A/G]AGAATAAAAAAAAAG | 74106 |
rs30752655 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165429352 | AATAAATCATACAAT[C/T]TTCATTGAAATTAAG | 74106 |
rs30755380 | snp | A/T | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165451979 | ATCCACACAAAATTA[A/T]AAAAAAAAAGTCTTA | 74106 |
rs30771635 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165356091 | CTACTAATTAAACAA[A/G]GCTGAATAAAAATAT | 74106 |
rs30907868 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Dcaf6 | Mm_Celera | 1:165385870 | ACCGAATCAAAGCTC[C/T]ATGAAGGCACCGACA | 74106 |
rs30909401 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dcaf6 | Mm_Celera | 1:165454939 | TTCGCCTCATAGCAC[A/G]AATCAAAAACTCTAC | 74106 |
rs30944614 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Dcaf6 | Mm_Celera | 1:165395766 | AAATGAAGGGGCCAT[A/G]TCTTTATATCATCAT | 74106 |
rs30958175 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Dcaf6 | Mm_Celera | 1:165423249 | TGAAAGGGCCCTAAG[A/G]TGTTACATATAGAAT | 74106 |
rs30989707 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165436604 | TTTAAATTCATGTTG[A/G]TCTCCTTGTCTCCCA | 74106 |
rs30995777 | snp | A/C | 0.32 | 0.24 | intron-variant | Dcaf6 | Mm_Celera | 1:165395210 | ACATCAGTCATTAAT[A/C]AAGAAAATGCCTCCA | 74106 |
rs31056550 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165436211 | ATTATCTTATACTTT[A/G]TAGATTACAAAATGG | 74106 |
rs31078939 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165436643 | TACCACCTTAAGAGA[A/G]CCTGAGTTGATCTTG | 74106 |
rs31091137 | snp | A/T | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165400968 | GCTGTCCTCAAACTC[A/T]GAAAACTGCCTGCCT | 74106 |
rs31095064 | snp | A/C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Dcaf6 | GRCm38.p3 | 1:165421762 | AGAACGCCACCTGGG[A/C/T]GCTGGCAGCTGAGCC | 74106 |
rs31137229 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dcaf6 | Mm_Celera | 1:165444356 | AAGATGGCTAAAAAT[A/G]CCAAACCAACCAAAC | 74106 |
rs31150532 | snp | G/T | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165438344 | AACAACTTCTACAAA[G/T]CTCTTTAATAAGGTC | 74106 |
rs31181453 | snp | A/G | 0.32 | 0.24 | intron-variant | Dcaf6 | Mm_Celera | 1:165354850 | AAAGTAGAAATGGTA[A/G]TCTTTGACAAACTGA | 74106 |
rs31209921 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Dcaf6 | Mm_Celera | 1:165332994 | CTCCCTCCACCTCCC[G/T]TGTGTTTAGGGAGTG | 74106 |
rs31235672 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Dcaf6 | Mm_Celera | 1:165427120 | GGTAATTACGGTAAT[A/G]AGACATGAAAGGGTG | 74106 |
rs31240028 | snp | G/T | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165343765 | TGTTAGAACACAGGG[G/T]TCACTTTAAACATTC | 74106 |
rs31276947 | snp | A/G | 0.32 | 0.24 | intron-variant | Dcaf6 | Mm_Celera | 1:165433131 | GCTGTGGGAAATGCA[A/G]GCTACTCTGAGTCAG | 74106 |
rs31277680 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dcaf6 | Mm_Celera | 1:165359482 | AAATAAAGACAATTA[C/T]ATAAATTCATATGCT | 74106 |
rs31308447 | snp | G/T | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165442327 | CCACAATGAGAATAT[G/T]TTTTTCCTTTGTTGG | 74106 |
rs31329904 | snp | A/C | 0.32 | 0.24 | intron-variant | Dcaf6 | Mm_Celera | 1:165396731 | CTTTCCCTACCCGCT[A/C]TCTCCTTTCACTCCA | 74106 |
rs31345927 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Mpc2, Dcaf6 | Mm_Celera | 1:165459578 | GGCTGGACCTGGGAA[A/G]GCGCGGGGGTGGGGA | 74106 |
rs31350935 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Dcaf6 | Mm_Celera | 1:165344341 | TTATTCTATCACCTA[C/T]TGTAGTTCCTCTGAT | 74106 |
rs31351897 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dcaf6 | Mm_Celera | 1:165335791 | CACACACACACACAC[A/G]CACACAAGAAGGAAG | 74106 |
rs31352794 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dcaf6 | Mm_Celera | 1:165426516 | GAGGCAGGCAGACCT[A/G]GGCAGCCTGGTCTGC | 74106 |
rs31354426 | snp | A/C/G | 0.32 | 0.24 | intron-variant | Dcaf6 | GRCm38.p3 | 1:165395029 | ACCTCGCAGCTTATC[A/C/G]TCAATCATGAAGGGA | 74106 |
rs31378092 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Dcaf6 | Mm_Celera | 1:165411769 | TTTTCTTGTAATTGA[C/T]TTTTAAAGACTGTTA | 74106 |
rs31382795 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Dcaf6 | Mm_Celera | 1:165401915 | CCAGCACTGGTCCTC[A/G]ATACACCCAACCTGC | 74106 |
rs31391325 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165452267 | CAGACATAATACAGA[C/T]TGAACACTGTACTGG | 74106 |
rs31401866 | snp | A/C | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165332726 | ACATGAAGGAAAACT[A/C]AGACACATAAAATAA | 74106 |
rs31403242 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165412812 | GTTTCTGGTACTTTT[C/T]AGTAAAAACAAAGTG | 74106 |
rs31410943 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dcaf6 | Mm_Celera | 1:165358915 | AACACAGAGTTTCCC[C/T]TTATTCTTTAGTTAT | 74106 |
rs31422554 | snp | A/T | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165352203 | GAAAAGCTATTTTTT[A/T]AAAAAAAATCACGCT | 74106 |
rs31427459 | snp | C/T | 0.32 | 0.24 | intron-variant | Dcaf6 | Mm_Celera | 1:165368920 | GGTATTAAGTAAAGA[C/T]CATCCTTAGCTGAAC | 74106 |
rs31435007 | snp | G/T | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165343876 | GTTATTTAGCTACTT[G/T]CAAGAAAGTGTCATT | 74106 |
rs31470355 | snp | A/C | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165396868 | ATCAGTTTATACACA[A/C]CAGAATTTAGTTTAA | 74106 |
rs31474990 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165395544 | TGTGTACCATGGCAT[A/G]TATACAGATGCATAC | 74106 |
rs31480540 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165386261 | TTACATTTCTTCCAG[A/G]CAACCTACATGTGCG | 74106 |
rs31498293 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Dcaf6 | Mm_Celera | 1:165401823 | GCCCAGAGGATGTGA[A/G]ACTGATTCTCAACAT | 74106 |
rs31499204 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Dcaf6 | Mm_Celera | 1:165424584 | GAAATCACTGTTATA[C/T]GCTAAAAGGCTCAAG | 74106 |
rs31500170 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Dcaf6 | Mm_Celera | 1:165387231 | ATTCAATACAACTTA[A/C]AACTAGTCTACAGAG | 74106 |
rs31528201 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165458751 | TTTACAGTGTAATCC[C/T]AGCTATCAGGAGAAT | 74106 |
rs31529311 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dcaf6 | Mm_Celera | 1:165431484 | TTTCTTAATGTTTTT[C/T]TAAATATTAAAGTGT | 74106 |
rs31532188 | snp | A/T | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165438388 | GTCAAGACTCATCTT[A/T]ACGTGTATGCTTGTA | 74106 |
rs31550237 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165393846 | GAGTGAGTGAGTGTG[C/T]GTGTGTGTGTGTGTG | 74106 |
rs31550387 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dcaf6 | Mm_Celera | 1:165435084 | CATTTGGTAGAAATC[C/T]TTTTTTTTTTTTTTT | 74106 |
rs31555905 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165352318 | TTAATGAGTGTGTGT[A/G]TGTGTGCGTTCTGGG | 74106 |
rs31566813 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dcaf6 | Mm_Celera | 1:165335521 | AGTCAGACTCAGAAA[A/G]ACAAACACAACATGC | 74106 |
rs31568539 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dcaf6 | Mm_Celera | 1:165444175 | CTGAGGACTGAACTC[A/G]GATCATCATTGGGCA | 74106 |
rs31574937 | snp | A/C | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165402027 | CCAAGAACATGGAGG[A/C]TGCAGAGACCAAGGC | 74106 |
rs31590724 | snp | A/G | 0.32 | 0.24 | intron-variant | Dcaf6 | Mm_Celera | 1:165433187 | ATTCTTAAGGCAGAA[A/G]TTGATTAACTGTGAA | 74106 |
rs31594751 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165424292 | AATTATACATATTTA[A/G]CCACTTTACCTTTCT | 74106 |
rs31597880 | snp | C/G/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Mpc2, Dcaf6 | GRCm38.p3 | 1:165461600 | CAGTTGAGTTGCTAC[C/G/T]GGAATCCCAGAGCCC | 74106 |
rs31604687 | snp | A/C | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165345241 | GAGATACCGTCTAAG[A/C]GAAAAGAGAGGTGCT | 74106 |
rs31604853 | snp | A/C | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165356062 | TTGTCATACTGTCAA[A/C]AAACATTCATATACT | 74106 |
rs31607277 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Dcaf6 | Mm_Celera | 1:165400992 | CCTGCCTCTGCCTCC[A/T]GAGTGCTGGGACTAA | 74106 |
rs31654691 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Dcaf6 | Mm_Celera | 1:165350230 | ACTATCCACCATACC[C/T]TTTTAGTTTCTTAAC | 74106 |
rs31670930 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dcaf6 | Mm_Celera | 1:165395734 | AAGACAGGAGGATGC[C/T]TGGAGCTTGCTGGCT | 74106 |