SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13459080 | snp | C/T | 0.474939 | 0.109099 | missense | Fbxo42 | Mm_Celera | 4:141199963 | GTCACGTGGATAGTA[C/T]AGACAACAGGACAGT | 213499 |
rs13471275 | snp | A/C | | | utr-variant-3-prime | Fbxo42 | Mm_Celera | 4:141202797 | TGCTGTGGGAAGTGA[A/C]TCAGCAGTGGAGACT | 213499 |
rs13471618 | snp | C/T | 0.444444 | 0.157135 | missense | Fbxo42 | Mm_Celera | 4:141200214 | GAAACAGTGCCCAAC[C/T]CCCGCCCAGGACCAG | 213499 |
rs13471619 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon | Fbxo42 | Mm_Celera | 4:141200264 | CTTACCCCCGATTGC[C/T]CGGCGCCTGGGCCAC | 213499 |
rs27571406 | snp | C/T | 0.5 | 0 | downstream-variant-500B | Fbxo42 | Mm_Celera | 4:141204445 | AGCAGGGCAGCTTCC[C/T]TCAGTGTGAGTGTAA | 213499 |
rs27571407 | snp | A/G | 0.265928 | 0.249492 | downstream-variant-500B | Fbxo42 | Mm_Celera | 4:141204207 | GGACTTTGTGGTGCA[A/G]ATTCTAAGGGAAGTG | 213499 |
rs27571408 | snp | A/G | 0.265928 | 0.249492 | utr-variant-3-prime | Fbxo42 | Mm_Celera | 4:141203136 | TCATTTGGTTGGCCT[A/G]TGAGAGTTCTGGGCG | 213499 |
rs27571409 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Fbxo42 | Mm_Celera | 4:141202070 | AAAACTGAAATTGAA[A/G]GGACAGCAGCGTGTT | 213499 |
rs27571410 | snp | A/G | 0.391111 | 0.206368 | utr-variant-3-prime | Fbxo42 | Mm_Celera | 4:141200911 | GGAAGCTGAAGAAGC[A/G]CCCCTGTGAGCTTTC | 213499 |
rs27571411 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Fbxo42 | Mm_Celera | 4:141200813 | ATCAGCTGTTGTGGT[C/T]TTAGTGGAGGCTGTG | 213499 |
rs27571412 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Fbxo42 | Mm_Celera | 4:141199285 | CTCAAACAGACGCCC[C/G]GATTCCACAGCTATA | 213499 |
rs27571413 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Fbxo42 | Mm_Celera | 4:141199062 | GTAAGTAGGGGATGA[A/G]CAGCCAGTAGGAAAT | 213499 |
rs27571414 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Fbxo42 | Mm_Celera | 4:141198640 | CATAGCTGAATGAAT[A/G]CCTGAGGGTTAGAAT | 213499 |
rs27571415 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Fbxo42 | Mm_Celera | 4:141198175 | CCCACTAAGACACAG[A/G]ACCCCTTCTCGGCAT | 213499 |
rs27571416 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxo42 | Mm_Celera | 4:141197924 | AGGCATAGAAACGCG[C/T]AGGCAGCTGGCATGC | 213499 |
rs27571417 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Fbxo42 | Mm_Celera | 4:141197464 | ACACCTTCCTTCTGA[C/T]TGTGTTCTTATCTCA | 213499 |
rs27571418 | snp | G/T | 0.497041 | 0.0383476 | intron-variant | Fbxo42 | Mm_Celera | 4:141197034 | CACAAGCCTGTTAGC[G/T]CCTGCACTGTGATGG | 213499 |
rs27571419 | snp | A/G | 0.5 | 0 | intron-variant | Fbxo42 | Mm_Celera | 4:141197011 | GAGGTGCTCTCTGTC[A/G]TCACCATCACAAGCC | 213499 |
rs27571420 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Fbxo42 | Mm_Celera | 4:141196987 | AGACTGCAGCTTATT[A/G]GCCACTGTGAGGTGC | 213499 |
rs27571421 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Fbxo42 | Mm_Celera | 4:141196732 | TCATGAAACCCTTGA[C/T]CTCATAAGTGCTGGG | 213499 |
rs27571422 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Fbxo42 | Mm_Celera | 4:141196179 | GACATGACCCACCAG[C/T]ATAGTGTTTTAAAAT | 213499 |
rs27571423 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Fbxo42 | Mm_Celera | 4:141195147 | AACAGGTGGGTCTGA[C/T]GTCTGCTTCCTTCCT | 213499 |
rs27571424 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxo42 | Mm_Celera | 4:141195112 | CCGCTCGCTCCTGCT[A/G]CCTTACATTCTGAGG | 213499 |
rs27571425 | snp | C/G | 0.304688 | 0.243945 | intron-variant | Fbxo42 | Mm_Celera | 4:141194990 | ACTTCTTCCTTGGCT[C/G]TCTGCAGCCACGCTG | 213499 |
rs27571426 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Fbxo42 | Mm_Celera | 4:141194345 | GTTTTGCAACGTGGT[C/T]TTAGGACATTAAGAC | 213499 |
rs27571427 | snp | A/G | 0.489796 | 0.070696 | synonymous-codon | Fbxo42 | Mm_Celera | 4:141193807 | TCACACGTACTCGCC[A/G]TCTAAAAACTGGTAA | 213499 |
rs27571428 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Fbxo42 | Mm_Celera | 4:141193314 | TAGTCCTCTGTTACC[C/T]GACATTCTCACTAGC | 213499 |
rs27571429 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Fbxo42 | Mm_Celera | 4:141192116 | TCTTCCACTTTACCT[A/G]TAAGTTCCAAGAGAG | 213499 |
rs27571430 | snp | A/T | 0.21875 | 0.248039 | intron-variant | Fbxo42 | Mm_Celera | 4:141190217 | GAGGGTAGAATTTTT[A/T]AAAAAAGCCCAGCAC | 213499 |
rs27571431 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Fbxo42 | Mm_Celera | 4:141189240 | TGTGTAACCACCACA[C/T]GCCCACAGGAACAAG | 213499 |
rs27571432 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Fbxo42 | Mm_Celera | 4:141188981 | CCAGTCTGTGTCACC[A/G]TGGCCAGCAGGAGGC | 213499 |
rs27571433 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fbxo42 | Mm_Celera | 4:141187631 | CAAGGCAGTTTAGAC[C/T]GTGCCCTCTTTAAAC | 213499 |
rs27571434 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Fbxo42 | Mm_Celera | 4:141187576 | CGAGCAGTGAGCAAT[A/G]TCATCTCATCCCTAA | 213499 |
rs27571435 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxo42 | Mm_Celera | 4:141186749 | GAAGGTCTGTGACTA[A/G]CAACATTGTCTTCTC | 213499 |
rs27571436 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fbxo42 | Mm_Celera | 4:141186583 | GGTTTTTCTAGACCA[C/T]GTGCTTTTTGGAGGT | 213499 |
rs27571437 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxo42 | Mm_Celera | 4:141186429 | TGTGTTTACAGGCTC[A/G]GTTTATTGATTACTC | 213499 |
rs27571438 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Fbxo42 | Mm_Celera | 4:141186391 | TTTTCCACCTCTCAT[C/T]GCTGCCTCTGGTTTC | 213499 |
rs27571439 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Fbxo42 | Mm_Celera | 4:141186323 | GCCTGTGTATCCTTC[C/T]CTTTCTGGCTGGCTC | 213499 |
rs27571440 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Fbxo42 | Mm_Celera | 4:141185546 | ACCCCGGGATAGCAA[G/T]TATCTTTACCATATG | 213499 |
rs27571441 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Fbxo42 | Mm_Celera | 4:141184915 | TTATGCCTTTGTGTT[A/G]AGTGTGTTGCGTGCC | 213499 |
rs27571442 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Fbxo42 | Mm_Celera | 4:141184747 | CTAGACTCTCTGCCC[C/T]AGTCTCCGCCAGTAC | 213499 |
rs27571443 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Fbxo42 | Mm_Celera | 4:141184498 | GCTTTATCCCTGGAC[A/G]CTTTTCACATAAGCG | 213499 |
rs27571444 | snp | C/T | 0.5 | 0 | intron-variant | Fbxo42 | Mm_Celera | 4:141184419 | CGTTTTATGTGTCTC[C/T]GGTGCCATCTGGATT | 213499 |
rs27571445 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Fbxo42 | Mm_Celera | 4:141184286 | CCTGGTTGCTCTTGG[A/G]TTCCCTCTGCAGTGA | 213499 |
rs27571446 | snp | G/T | 0.5 | 0 | intron-variant | Fbxo42 | Mm_Celera | 4:141184174 | ACTCTGAGTCATTTA[G/T]TCAAATTCGGGAGCC | 213499 |
rs27571447 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Fbxo42 | Mm_Celera | 4:141184147 | GTCATTGACTCCTCC[C/T]ACTATCCTTTGACTC | 213499 |
rs27571448 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fbxo42 | Mm_Celera | 4:141183988 | GGCTCTCTCTCCAGC[C/T]CTTAGTCCCACTGTG | 213499 |
rs27571449 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Fbxo42 | Mm_Celera | 4:141182445 | AACAACTTGGGTTTT[C/G]TTCAGAAATATCCCA | 213499 |
rs27571450 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Fbxo42 | Mm_Celera | 4:141182417 | AGGCCAGCCAGACAC[A/T]GCAGCACACACAAAC | 213499 |
rs27571451 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Fbxo42 | Mm_Celera | 4:141182341 | CTTTTGCTTTCCTAC[C/T]CCAGTATATGCTCCA | 213499 |
rs27571452 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Fbxo42 | Mm_Celera | 4:141182156 | ACACGATGTGACAAT[C/T]ATTCATCTTGCTTTT | 213499 |
rs27571453 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Fbxo42 | Mm_Celera | 4:141181738 | CGGAAGTATGGCTAA[A/C]TGCTCCTCTTTTAGG | 213499 |
rs27571454 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Fbxo42 | Mm_Celera | 4:141181537 | CTGTGACTTACAAGT[A/G]TGGACTGCAGGATCC | 213499 |
rs27571455 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Fbxo42 | Mm_Celera | 4:141181514 | GCCATGATCTCAGTT[C/T]CCAGTGACTGTGACT | 213499 |
rs27571456 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Fbxo42 | Mm_Celera | 4:141181354 | TTCGGCTTTCGAGGA[C/T]GGAACTAACCGAGTC | 213499 |
rs27571457 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Fbxo42 | Mm_Celera | 4:141181309 | GATGCTCTGCTAGAT[A/T]GATTGGCAGGCTTTC | 213499 |
rs27571458 | snp | G/T | 0.5 | 0 | intron-variant | Fbxo42 | Mm_Celera | 4:141181101 | TAGCAGGTGCATTCC[G/T]AGCCGGTCCCAGGAT | 213499 |
rs27571459 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxo42 | Mm_Celera | 4:141181089 | GGGAAGGTTTCATAG[C/T]AGGTGCATTCCGAGC | 213499 |
rs27571460 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Fbxo42 | Mm_Celera | 4:141181000 | GGCTGAGGTCTCTGA[A/G]TAACAGTTGCTCTTG | 213499 |
rs27571461 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Fbxo42 | Mm_Celera | 4:141180915 | AGGTGTGATTTGTGT[C/T]TGGAATGAAGTTGAA | 213499 |
rs27571462 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Fbxo42 | Mm_Celera | 4:141180869 | GTGGCACTGTGTGAA[C/T]CCATGGTGTGGTTTT | 213499 |
rs27571463 | snp | C/T | 0.497778 | 0.0332592 | synonymous-codon | Fbxo42 | Mm_Celera | 4:141180438 | GTCTATGTATGTCTT[C/T]GGTGGCTGTACGCAG | 213499 |
rs27571464 | snp | C/T | 0.5 | 0 | intron-variant | Fbxo42 | Mm_Celera | 4:141180381 | ACTTGTTTGTTGTGT[C/T]TCTCTGCCCCCTGTA | 213499 |
rs27571465 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Fbxo42 | Mm_Celera | 4:141179651 | ACTCAGAATGCCACC[A/G]TCTGAATGCCACCGA | 213499 |
rs27571466 | snp | A/C | 0.290657 | 0.246672 | intron-variant | Fbxo42 | Mm_Celera | 4:141179505 | AAAGATTTGTGCTTT[A/C]GGTTACATTTAGAAA | 213499 |
rs27571467 | snp | G/T | 0.359862 | 0.224567 | intron-variant | Fbxo42 | Mm_Celera | 4:141179369 | TCAATAGCTTCTTGC[G/T]TCTTCCTTCAATTGC | 213499 |
rs27571468 | snp | A/C | 0.497778 | 0.0332592 | intron-variant | Fbxo42 | Mm_Celera | 4:141179142 | GCAGGGCTTGTGTTC[A/C]TCTTGTCCTAGGGAC | 213499 |
rs27571469 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Fbxo42 | Mm_Celera | 4:141179083 | TGTAGACACAGGGAA[C/G]CTTGCTCAGTCTCTT | 213499 |
rs27571470 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxo42 | Mm_Celera | 4:141178797 | GCTGGCCAAATGAGA[A/G]AAACGGGGCACCTCC | 213499 |
rs27571471 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxo42 | Mm_Celera | 4:141178608 | ACTGGAGTGGGTACT[A/G]GGCAATCGTGAGAGC | 213499 |
rs27571472 | snp | A/G | 0.5 | 0 | intron-variant | Fbxo42 | Mm_Celera | 4:141177325 | TCCTCCTAGTGCTCA[A/G]GAGGTCACCACAAGC | 213499 |
rs27571473 | snp | A/T | 0.5 | 0 | intron-variant | Fbxo42 | Mm_Celera | 4:141176511 | CAGTAAGCAGAGTGA[A/T]TGGGGTGCTTGCTAG | 213499 |
rs27571474 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxo42 | Mm_Celera | 4:141176456 | CCTCATCTCGTGGGG[C/T]GTTCCCGCTGCTGTC | 213499 |
rs27571475 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Fbxo42 | Mm_Celera | 4:141176315 | AATCTTAGTGCAGTA[C/T]TCACACTGCTGTGAG | 213499 |
rs27571476 | snp | C/T | 0.5 | 0 | intron-variant | Fbxo42 | Mm_Celera | 4:141176246 | TAAGTGTCTTTGTTA[C/T]AGTTGTTCGTGTACA | 213499 |
rs27571477 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Fbxo42 | Mm_Celera | 4:141176222 | CTGGATAGTGTTGGC[A/G]ACTTGAGATAAGTGT | 213499 |
rs27571478 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Fbxo42 | Mm_Celera | 4:141175987 | CACATGACAGCATCG[C/T]TTCTTCCAGCATGGG | 213499 |
rs27571479 | snp | G/T | 0.49827 | 0.0293608 | intron-variant | Fbxo42 | Mm_Celera | 4:141175703 | GCCAGGGACAGAAAA[G/T]GCAGGTGAAGTTTCA | 213499 |
rs27571480 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Fbxo42 | Mm_Celera | 4:141174953 | AGTGTTATTCTTTCT[C/T]AAATAGTTGTTATTC | 213499 |
rs27571481 | snp | C/T | 0.495 | 0.0497494 | intron-variant | Fbxo42 | Mm_Celera | 4:141174914 | TACTCAGCAAAGATA[C/T]TGGCAGAATTGTTTT | 213499 |
rs27571482 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Fbxo42 | Mm_Celera | 4:141174497 | TGTTTATGAAGTATG[A/G]TTGAGAAAAAATCAT | 213499 |
rs27571483 | snp | C/T | 0.495 | 0.0497494 | intron-variant | Fbxo42 | Mm_Celera | 4:141174470 | TGTATTTGTAAGATG[C/T]ATGTGGCAAATTGTT | 213499 |
rs27571484 | snp | A/G | 0.5 | 0 | intron-variant | Fbxo42 | Mm_Celera | 4:141174102 | CCTCCGCCCTTTTCT[A/G]TTTCCCTTTCTCAGT | 213499 |
rs27571485 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Fbxo42 | Mm_Celera | 4:141174091 | TGTCTATTGTGCCTC[A/C]GCCCTTTTCTGTTTC | 213499 |
rs27571486 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Fbxo42 | Mm_Celera | 4:141173923 | TTGGATTCATTCTCA[A/G]ATCTTGCCCTCAGGA | 213499 |
rs27571487 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Fbxo42 | Mm_Celera | 4:141173879 | TTTAGTGAATGTCTC[C/T]ATCATCTTAAATACA | 213499 |
rs27571488 | snp | A/T | 0.495868 | 0.0452663 | intron-variant | Fbxo42 | Mm_Celera | 4:141173794 | TGTTACCATGGAGAT[A/T]CTGGATGTTCATACT | 213499 |
rs27571489 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxo42 | Mm_Celera | 4:141172632 | GTGTGTGAAGGGAAC[A/G]GCTCTTACTTCAAGC | 213499 |
rs27571490 | snp | A/G | 0.5 | 0 | intron-variant | Fbxo42 | Mm_Celera | 4:141172575 | GAGTCTGCCTGTGTC[A/G]GCCAGCTTCCTGTAA | 213499 |
rs27571491 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Fbxo42 | Mm_Celera | 4:141172541 | CCTGGCCCTAAAAGT[A/G]TCCTGCAGTGAGGAG | 213499 |
rs27571492 | snp | A/T | 0.21875 | 0.248039 | intron-variant | Fbxo42 | Mm_Celera | 4:141172535 | CTATATCCTGGCCCT[A/T]AAAGTGTCCTGCAGT | 213499 |
rs27571493 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Fbxo42 | Mm_Celera | 4:141172408 | TAGTTACTACTACAG[A/G]TGGTAGGAAAGATGC | 213499 |
rs27571494 | snp | G/T | 0.32 | 0.24 | intron-variant | Fbxo42 | GRCm38.p3 | 4:141172395 | TGACTCAGTGTGTTA[G/T]TTACTACTACAGATG | 213499 |
rs27571495 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Fbxo42 | Mm_Celera | 4:141172359 | CTGGGCTGGGTGACG[C/T]TCTCTCGCAGGAGCC | 213499 |
rs27571496 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxo42 | Mm_Celera | 4:141172314 | AAGATCTCAAGTGTT[C/T]CTGAAGTTTGCAGAT | 213499 |
rs27571497 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Fbxo42 | Mm_Celera | 4:141172017 | TCTGACCTCCATTCA[C/G]TGTGGCTTATAGCTC | 213499 |
rs27571498 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Fbxo42 | Mm_Celera | 4:141171798 | AGGAGGGGACACCTG[C/G]GAGTCTTCTATGGGA | 213499 |
rs27571499 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxo42 | Mm_Celera | 4:141171727 | CCAAGGAGACAGATG[A/G]GAGATGAAGTGTCCC | 213499 |
rs27571500 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fbxo42 | Mm_Celera | 4:141171625 | GATCCTTCAGTGCCA[C/G]CTACCCCAGGTCTCT | 213499 |
rs27571501 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fbxo42 | Mm_Celera | 4:141171463 | GACTTGGTAGACCCA[G/T]TCACACTGTCAGCTG | 213499 |