SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs30108042 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Pdlim2 | Mm_Celera | 14:70166805 | CGGAAAACCTTTTTA[C/T]TTAGCCCCGTGTTCC | 213019 |
rs30163170 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Pdlim2 | Mm_Celera | 14:70166897 | GCAGCTCCAAGCCCT[A/G]TTCTGCCAGCATCAT | 213019 |
rs30198139 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Pdlim2 | Mm_Celera | 14:70170689 | GTTGTCATCTGCCCC[A/G]CCCCAGTCCTTGGGG | 213019 |
rs30241874 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Pdlim2 | Mm_Celera | 14:70170653 | CCAGCCACTCTGCCC[C/G]AGCGGCTGATGGCCA | 213019 |
rs30346754 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Pdlim2 | Mm_Celera | 14:70165351 | ACACTGTTACACCCT[A/G]AGCCGGGCAAGCTCC | 213019 |
rs30387193 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon | Pdlim2 | Mm_Celera | 14:70171742 | TGCCAGCACTTCCAA[A/G]GAGCCCTCCCCATTG | 213019 |
rs30404696 | snp | A/T | 0.475309 | 0.108333 | intron-variant | Pdlim2 | Mm_Celera | 14:70165762 | GGAGAGATGTGAGCA[A/T]TTTTTTTTTAACCAG | 213019 |
rs30407942 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Pdlim2 | Mm_Celera | 14:70170694 | CATCTGCCCCGCCCC[A/G]GTCCTTGGGGGAGGA | 213019 |
rs30481723 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Pdlim2 | Mm_Celera | 14:70175769 | CAGCAAGAAGTTAGC[A/G]GAGGCTGGGGCTGGC | 213019 |
rs30569492 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Pdlim2 | Mm_Celera | 14:70168251 | AGGGAAGAGACGCCC[A/G]TTGCCGGATAAAGAG | 213019 |
rs30572639 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Pdlim2 | Mm_Celera | 14:70168633 | CTGAGTTCAAATCCT[A/G]GCAACCACATGGTGG | 213019 |
rs30583469 | snp | A/C | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Pdlim2 | Mm_Celera | 14:70174966 | ACCCTAAATGGCTGC[A/C]GGCAGGTGTGAGGGT | 213019 |
rs30624611 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Pdlim2 | Mm_Celera | 14:70165222 | TCGAACTCAGAAATC[C/T]GCCTGCGTGTGCTAT | 213019 |
rs30634170 | snp | C/T | 0.5 | 0 | intron-variant | Pdlim2 | Mm_Celera | 14:70165176 | TGTAGCCCTGGCTGT[C/T]CTGGGACTCACTCTG | 213019 |
rs30647555 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Pdlim2 | Mm_Celera | 14:70172064 | CATCCCTCCTTTCTT[C/T]CATTTCATCTAGACT | 213019 |
rs30839758 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Pdlim2 | Mm_Celera | 14:70174925 | AAGCTCCCAAGAGCA[A/G]GCAGAAGCACCTGCC | 213019 |
rs30846532 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pdlim2 | Mm_Celera | 14:70173818 | AGTGTAGGGACCCAC[A/G]TTCAATGGCAAAGCC | 213019 |
rs30871592 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Pdlim2 | Mm_Celera | 14:70171822 | GAGATGGTCTGTCAC[A/G]GGATCCTAGACTTCA | 213019 |
rs30873904 | snp | C/T | 0.375 | 0.216506 | intron-variant | Pdlim2 | Mm_Celera | 14:70174772 | CAGAATGTCAGGAAC[C/T]GAGCTTGGGAATACT | 213019 |
rs30974783 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Pdlim2 | Mm_Celera | 14:70171965 | ACCACCATTCCTCTC[A/G]GGTTCAGCACTATAG | 213019 |
rs31037659 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Pdlim2 | Mm_Celera | 14:70175011 | AAGGGCAGGCCCTGT[C/T]CTTGGTCCCCTTCCT | 213019 |
rs31085601 | snp | A/C | 0.375 | 0.216506 | intron-variant | Pdlim2 | Mm_Celera | 14:70174621 | AAACAAGACAGTACA[A/C]CTCTACCACCTTTTT | 213019 |
rs31120565 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Pdlim2 | Mm_Celera | 14:70165339 | TAATTAAAAGTAACA[C/T]TGTTACACCCTAAGC | 213019 |
rs31148506 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Pdlim2 | Mm_Celera | 14:70166397 | AGTAAAGGAGAAGAG[A/G]CAGAGCCTTGGCAAA | 213019 |
rs31232774 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Pdlim2 | Mm_Celera | 14:70174922 | AGCAAGCTCCCAAGA[A/G]CAAGCAGAAGCACCT | 213019 |
rs31255303 | snp | A/G | 0.415225 | 0.187619 | synonymous-codon | Pdlim2 | GRCm38.p3 | 14:70164745 | GTCTGCGCAAGTGTA[A/G]CAGCCAGGGTGTCGG | 213019 |
rs31256138 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pdlim2 | Mm_Celera | 14:70171640 | GGCCAAGAAAGAGTT[A/G]GCATGACCCTGCTGG | 213019 |
rs31273166 | snp | C/T | 0.375 | 0.216506 | missense, intron-variant | Pdlim2 | Mm_Celera | 14:70171503 | GGGCAACTGGGCTGG[C/T]AGGGGGTGGGGTGGA | 213019 |
rs31278383 | snp | G/T | 0.5 | 0 | intron-variant | Pdlim2 | Mm_Celera | 14:70164973 | ACAAAGGATCAACAT[G/T]CATATGCACAACCCC | 213019 |
rs31327397 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Pdlim2 | Mm_Celera | 14:70167043 | ATATCTCCAATCCTC[A/G]GGGGTCGAGGTCGGG | 213019 |
rs31354891 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon | Pdlim2 | GRCm38.p3 | 14:70164685 | CTCGCAGTACAACTC[A/G]TTGCCCACCCAGAAG | 213019 |
rs31378129 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pdlim2 | Mm_Celera | 14:70171849 | TTCACCCTACCTGAA[C/T]ACTGTTCCTAGGCCC | 213019 |
rs31411756 | snp | A/G | 0.444444 | 0.157135 | downstream-variant-500B | Pdlim2 | Mm_Celera | 14:70164001 | GGAGGAAGAGGAAGA[A/G]GAAGAAGAAGAAGCA | 213019 |
rs31411757 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pdlim2 | Mm_Celera | 14:70174065 | GGAACCAGTCAAACC[C/T]GGGCTTCCAGGTAGC | 213019 |
rs31500875 | snp | G/T | 0.444444 | 0.157135 | downstream-variant-500B | Pdlim2 | Mm_Celera | 14:70163771 | TGGAGAGATGGCTCA[G/T]CGGTTAAGAGCACTG | 213019 |
rs36370548 | snp | A/G | 0.244898 | 0.249948 | synonymous-codon | Pdlim2 | Mm_Celera | 14:70166170 | GGGCAAGGAAGCCTG[A/G]GAGCTCAGCGAGCTG | 213019 |
rs36543235 | snp | A/G | 0.297521 | 0.245442 | upstream-variant-2KB | Pdlim2 | Mm_Celera | 14:70179528 | CCCGTCATCAACCCT[A/G]CCTCAGATAAGGGCA | 213019 |
rs36565116 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pdlim2 | Mm_Celera | 14:70170573 | CTTTGGAATGCAGAG[C/T]CAACCCAGAAGTAAG | 213019 |
rs36613078 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Pdlim2 | Mm_Celera | 14:70169997 | GTTTGCTCAGATGGG[A/C]CACTACAGGAAGACA | 213019 |
rs36712546 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Pdlim2 | Mm_Celera | 14:70167891 | AAGGGGCGGAGACTC[C/G]CATCCCTCTCTAGGA | 213019 |
rs36746315 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Pdlim2 | Mm_Celera | 14:70165996 | TTGAACTGGATGCCA[C/T]TTGGCCATGCTGCCC | 213019 |
rs36754929 | snp | C/T | 0.489796 | 0.070696 | upstream-variant-2KB | Pdlim2 | Mm_Celera | 14:70179515 | GTGCATCACTCTTCC[C/T]GTCATCAACCCTGCC | 213019 |
rs36768151 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Pdlim2 | Mm_Celera | 14:70166499 | AGGTGTTGTCTCTCC[A/G]TGGGCCAGTCATGAT | 213019 |
rs36769625 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Pdlim2 | Mm_Celera | 14:70167577 | TAGTTCTGCCATGGA[C/T]CCTTAAGCTACTTCC | 213019 |
rs36803423 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime | Pdlim2 | Mm_Celera | 14:70164245 | CTTAATTTTATCCAC[A/G]TGTATATAGAGTTCA | 213019 |
rs36815769 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Pdlim2 | Mm_Celera | 14:70166619 | AGCCAGCGAGAACAC[C/T]AAGATGAAGCACAAA | 213019 |
rs36921436 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Pdlim2 | Mm_Celera | 14:70171451 | GCCAGGGTACTCAGC[A/C]ATGCTCACCTACAGC | 213019 |
rs36961489 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pdlim2 | Mm_Celera | 14:70170725 | GAAATACCACCTGGG[A/G]GTTAAGCTGTCAGCA | 213019 |
rs36979927 | snp | C/T | 0.408163 | 0.193609 | missense, intron-variant | Pdlim2 | Mm_Celera | 14:70171481 | CCAATCATATCCTCT[C/T]TAGAAAGGGCAACTG | 213019 |
rs37070592 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Pdlim2 | Mm_Celera | 14:70170252 | CTCGGGCCACCCAAC[C/T]TACTTGTCTTTCTCC | 213019 |
rs37193219 | snp | A/G | 0.426035 | 0.177515 | utr-variant-3-prime | Pdlim2 | GRCm38.p3 | 14:70164368 | CGTGTCAAACATGGC[A/G]GCCACTGTAGACCGT | 213019 |
rs37328962 | snp | C/T | 0.459184 | 0.136902 | upstream-variant-2KB | Pdlim2 | Mm_Celera | 14:70179545 | CTCAGATAAGGGCAC[C/T]TTAAGTGACAGGTCA | 213019 |
rs37329846 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pdlim2 | Mm_Celera | 14:70166260 | TGTCCACCACAGAGG[C/T]ATCCAGCTATACACA | 213019 |
rs37398945 | snp | C/T | 0.132653 | 0.220748 | missense | Pdlim2 | Mm_Celera | 14:70171272 | TGAGCAGCAGCAAGG[C/T]CTGGAGAGTGTGTCA | 213019 |
rs37619257 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Pdlim2 | Mm_Celera | 14:70166428 | GGCTGATGAAGAACC[C/T]TATCCTTCCAAAGCA | 213019 |
rs37752889 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Pdlim2 | Mm_Celera | 14:70165848 | AAAAGAGCAGGCTTT[G/T]CTAAGAGGAGGGAGG | 213019 |
rs38124579 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Pdlim2 | Mm_Celera | 14:70165815 | TCACCCATTGAGAAA[G/T]GAGCCTAGGATAGGG | 213019 |
rs38357345 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Pdlim2 | Mm_Celera | 14:70165672 | ACACTATCCTGTCCC[A/G]CCAATGAGAAAGTAG | 213019 |
rs38399906 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Pdlim2 | Mm_Celera | 14:70165568 | TTGTGTGTTCTGTGC[A/G]TTACAAGCCCTCCAG | 213019 |
rs38978480 | snp | C/T | 0.197531 | 0.244432 | upstream-variant-2KB | Pdlim2 | Mm_Celera | 14:70179686 | TTGGTAAGCAGGCGG[C/T]AGGCAGTGATAAGGT | 213019 |
rs39468210 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Pdlim2 | Mm_Celera | 14:70171110 | GCTAGCTTCTCTGGC[C/T]GGCTCAGGGGTATAA | 213019 |
rs39811570 | snp | A/G | 0.396694 | 0.202437 | upstream-variant-2KB | Pdlim2 | Mm_Celera | 14:70179437 | ACACCCAGGCTCAAG[A/G]AACCAGCCAGGGCCA | 213019 |
rs40243462 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pdlim2 | Mm_Celera | 14:70171071 | CGACAGGAGAGAGGA[C/T]GACTGCAAGTGGCCT | 213019 |
rs45653873 | snp | A/G | | | intron-variant | Pdlim2 | Mm_Celera | 14:70173469 | CATGAGGCCCCCTCC[A/G]CCCTCCTCCTCTTCT | 213019 |
rs46267602 | snp | A/C | | | intron-variant | Pdlim2 | Mm_Celera | 14:70170160 | CCTAGAACTTCAGAC[A/C]ACTGCACCTCATTCT | 213019 |
rs46328369 | snp | C/T | | | upstream-variant-2KB | Pdlim2 | Mm_Celera | 14:70179621 | GTCCCTCCCCAAGTC[C/T]GACGTGATTCTCCTG | 213019 |
rs46439614 | snp | C/T | | | intron-variant | Pdlim2 | Mm_Celera | 14:70169881 | TGAGTCCCCAATTCC[C/T]ACTCTGCAGCAAGTC | 213019 |
rs46481171 | snp | A/C/T | | | synonymous-codon, intron-variant | Pdlim2 | GRCm38.p3 | 14:70171531 | GGAGAAGGGGCTGCA[A/C/T]GGCCTGGGGCTGAGA | 213019 |
rs47002117 | snp | C/T | | | upstream-variant-2KB | Pdlim2 | Mm_Celera | 14:70179683 | CACTTGGTAAGCAGG[C/T]GGTAGGCAGTGATAA | 213019 |
rs47027866 | snp | C/T | | | upstream-variant-2KB | Pdlim2 | Mm_Celera | 14:70179624 | CCTCCCCAAGTCCGA[C/T]GTGATTCTCCTGCTC | 213019 |
rs47215467 | snp | G/T | | | intron-variant | Pdlim2 | Mm_Celera | 14:70171412 | GACTCCGAGGGGCCA[G/T]GCTCAAACTTGGTGG | 213019 |
rs47215956 | snp | G/T | | | intron-variant | Pdlim2 | Mm_Celera | 14:70169402 | AATTCTGTTTTTTTG[G/T]TTTTTTCCATGAATG | 213019 |
rs47250229 | snp | G/T | | | upstream-variant-2KB | Pdlim2 | Mm_Celera | 14:70179675 | TTTCAGGGCACTTGG[G/T]AAGCAGGCGGTAGGC | 213019 |
rs48200547 | snp | A/G | | | upstream-variant-2KB | Pdlim2 | Mm_Celera | 14:70179691 | AAGCAGGCGGTAGGC[A/G]GTGATAAGGTTGAGC | 213019 |
rs48731572 | snp | A/C | | | intron-variant | Pdlim2 | Mm_Celera | 14:70164985 | CATTCATATGCACAA[A/C]CCCCTGACTGGGACT | 213019 |
rs49193119 | snp | A/C | | | downstream-variant-500B | Pdlim2 | Mm_Celera | 14:70163867 | CCGAGATCTGATGCC[A/C]TCTTCTGGAGTGTCT | 213019 |
rs49540473 | snp | C/T | | | intron-variant | Pdlim2 | Mm_Celera | 14:70169885 | TCCCCAATTCCTACT[C/T]TGCAGCAAGTCCAGG | 213019 |
rs49984392 | snp | A/C | | | intron-variant | Pdlim2 | Mm_Celera | 14:70169836 | AAACAAAAACAAAAA[A/C]AAAAAAAAAACCCCA | 213019 |
rs50004120 | snp | A/G | | | intron-variant | Pdlim2 | Mm_Celera | 14:70170455 | AGCACCACAAATTGA[A/G]CCCCTTCCTTCTCCA | 213019 |
rs50089789 | snp | A/G | | | upstream-variant-2KB | Pdlim2 | Mm_Celera | 14:70179677 | TCAGGGCACTTGGTA[A/G]GCAGGCGGTAGGCAG | 213019 |
rs50460018 | snp | C/T | | | utr-variant-3-prime | Pdlim2 | GRCm38.p3 | 14:70164376 | ACATGGCAGCCACTG[C/T]AGACCGTAATACAGA | 213019 |
rs50781411 | snp | C/G | | | intron-variant | Pdlim2 | Mm_Celera | 14:70173338 | TGTGGAGCTGGCCAG[C/G]CCCCCATTCCCCAGT | 213019 |
rs51562028 | snp | C/T | | | intron-variant | Pdlim2 | Mm_Celera | 14:70173110 | CCTCCTGCTCACCAT[C/T]ATACTACATTCCTGG | 213019 |
rs51663195 | snp | A/G | | | intron-variant | Pdlim2 | Mm_Celera | 14:70165893 | ACAGAGGCTTGGGGA[A/G]CAGGTACGAAAACCC | 213019 |
rs51707912 | snp | C/G | | | intron-variant | Pdlim2 | Mm_Celera | 14:70169900 | CTGCAGCAAGTCCAG[C/G]CTGGGGCCCCGGAGA | 213019 |
rs52171650 | snp | C/G | | | intron-variant | Pdlim2 | Mm_Celera | 14:70169716 | CTCCAGGAGGCCAAG[C/G]CAGGCAGATCTCTGT | 213019 |
rs52250768 | snp | A/C | | | intron-variant | Pdlim2 | Mm_Celera | 14:70172595 | AGACAGAGAGAGAGA[A/C]AGAGAGACAGAGAGA | 213019 |
rs211738087 | snp | C/T | | | intron-variant, upstream-variant-2KB | Pdlim2 | Mm_Celera | 14:70175563 | CAGCAGTCCCACTGA[C/T]AAGAGGTCAGACTTC | 213019 |
rs211738138 | snp | A/G | | | downstream-variant-500B | Pdlim2 | Mm_Celera | 14:70164217 | AAAGGGAAAGAAGGA[A/G]GAAAATACACTACTT | 213019 |
rs212076282 | snp | C/T | | | intron-variant | Pdlim2 | Mm_Celera | 14:70174128 | GCATGCCCAGCCCGG[C/T]GCCCACCTATGCCCA | 213019 |
rs212150985 | in-del | -/A | | | intron-variant | Pdlim2 | Mm_Celera | 14:70169105 | AAATAAATAAATCTT[-/A]AAAAAAAAAAAAGAA | 213019 |
rs212164631 | snp | G/T | | | upstream-variant-2KB, intron-variant | Pdlim2 | Mm_Celera | 14:70177448 | CCTCCTCTCCCACCA[G/T]TCTGCCTGGCATGGG | 213019 |
rs212497528 | snp | A/G | | | upstream-variant-2KB | Pdlim2 | GRCm38.p3 | 14:70178816 | CCATCTCATCCAATC[A/G]ATGATTCAAACAATC | 213019 |
rs212548164 | in-del | -/TT | | | intron-variant | Pdlim2 | Mm_Celera | 14:70165921 | CCAAAAGTGCTAGCA[-/TT]TTTTTTTTTCATTCC | 213019 |
rs213148653 | snp | A/G | | | intron-variant | Pdlim2 | Mm_Celera | 14:70171183 | GCTAGTGGCTCGGGA[A/G]GCAGGTCTCTCATCT | 213019 |
rs213209729 | snp | A/G | | | intron-variant | Pdlim2 | GRCm38.p3 | 14:70171861 | GAATACTGTTCCTAG[A/G]CCCGGGCCTTCAGAC | 213019 |
rs213877842 | snp | A/G | | | intron-variant | Pdlim2 | GRCm38.p3 | 14:70171367 | CCCCAGGGAGGAGGG[A/G]GCCCAGGGTCCCCTA | 213019 |
rs214265737 | snp | A/G | | | intron-variant | Pdlim2 | Mm_Celera | 14:70166320 | CCCCAGGACACGCCC[A/G]CTCTTGTGGCCAAAG | 213019 |
rs214331507 | snp | C/T | | | intron-variant | Pdlim2 | Mm_Celera | 14:70166903 | CCAAGCCCTATTCTG[C/T]CAGCATCATCCTCTC | 213019 |
rs214334934 | in-del | -/AGAGAG | | | upstream-variant-2KB, intron-variant | Pdlim2 | Mm_Celera | 14:70177404 | AGACCCAGAGGAGAT[-/AGAGAG]AGAGAGCACTTGGCA | 213019 |