SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13460316 | snp | G/T | | | synonymous-codon | Pcgf2 | Mm_Celera | 11:97690047 | GAACTGCCTGCAAAC[G/T]CCATCCTCCACCAGC | 22658 |
rs27089799 | snp | C/T | 0.46875 | 0.121031 | upstream-variant-2KB | Psmb3, Pcgf2 | Mm_Celera | 11:97702595 | CAAGACCAGTCACGA[C/T]GCAAGCAGTTACAGT | 22658 |
rs27089800 | snp | A/G | 0.18 | 0.24 | upstream-variant-2KB | Pcgf2, Psmb3 | Mm_Celera | 11:97701874 | TAGTTAGAGAGAGTC[A/G]TTCCTTCTTGCTTTT | 22658 |
rs27089801 | snp | C/T | 0.21875 | 0.248039 | upstream-variant-2KB | Pcgf2, Psmb3 | Mm_Celera | 11:97701719 | TACCCTGTCCTCTAG[C/T]TGATTGCCACACGTA | 22658 |
rs29385984 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Pcgf2, Psmb3 | Mm_Celera | 11:97702387 | TATTGCTTCTGGTAC[C/T]TCGGTACCGAATGTG | 22658 |
rs29393587 | snp | C/T | 0.375 | 0.216506 | intron-variant | Pcgf2 | Mm_Celera | 11:97695405 | TGCTGTCTGGGCTTC[C/T]GAAGGTACTCCATGT | 22658 |
rs29396723 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pcgf2 | GRCm38.p3 | 11:97697166 | TCTGCACCAGGACAC[A/G]AAATCTCTTATCTTT | 22658 |
rs29400651 | snp | A/G | 0.32 | 0.24 | intron-variant | Pcgf2 | Mm_Celera | 11:97698204 | TTGGAGCAGGGATGT[A/G]TGTATGTTGGGGGTG | 22658 |
rs29409633 | snp | C/T | 0.375 | 0.216506 | intron-variant | Pcgf2 | Mm_Celera | 11:97690566 | GGAAGGAAGGTATTA[C/T]GTTCCACTGTAGCCG | 22658 |
rs29422218 | snp | A/G | 0.375 | 0.216506 | intron-variant | Pcgf2 | Mm_Celera | 11:97698561 | CCTGGGAGTCAGGAA[A/G]GGCGCGGGGCGTCTG | 22658 |
rs29430304 | snp | A/T | 0.375 | 0.216506 | intron-variant | Pcgf2 | Mm_Celera | 11:97693220 | TGAGGTTTCTGATGC[A/T]GTCCCAGGAGTGAGC | 22658 |
rs29433257 | snp | C/T | 0.375 | 0.216506 | intron-variant | Pcgf2 | Mm_Celera | 11:97690510 | GAGACAGAGACCCAG[C/T]GAAGAAAGAGTGTGG | 22658 |
rs29437313 | snp | A/C | 0.375 | 0.216506 | upstream-variant-2KB | Pcgf2, Psmb3 | Mm_Celera | 11:97702233 | TGGCAGTGAGACAGA[A/C]ACTTGGCTTTGCCTT | 22658 |
rs29471050 | snp | A/C | 0.375 | 0.216506 | intron-variant | Pcgf2 | Mm_Celera | 11:97698481 | TTCTCGATCAAGCAA[A/C]CACAGCAATTTTGGA | 22658 |
rs29473649 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Pcgf2 | Mm_Celera | 11:97693789 | AAGTAAGGTCATATA[A/C]CATTTAGAAGCAGTA | 22658 |
rs29480167 | snp | A/G | 0.375 | 0.216506 | intron-variant | Pcgf2 | Mm_Celera | 11:97698298 | AAGACTGTGAGAGCC[A/G]GCTAAGAGAAGCCCC | 22658 |
rs29483916 | snp | A/G | 0.375 | 0.216506 | intron-variant | Pcgf2 | Mm_Celera | 11:97690693 | AGGCTGAGGAAGGAC[A/G]ACTGCTCTGAATTCG | 22658 |
rs46554698 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | Pcgf2 | Mm_Celera | 11:97700639 | AGAGCTAGAAGAGAC[A/G]GCGCCAAGGAAGCGA | 22658 |
rs49680849 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97692217 | TAGGGCAGCTCAGAG[A/G]TTGAGCCCAGTCCCC | 22658 |
rs49845579 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | Pcgf2 | Mm_Celera | 11:97700605 | CCAGCGGCTCCGGGC[C/T]CCGGGCAGAGTAGGA | 22658 |
rs50934847 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | Pcgf2 | Mm_Celera | 11:97700967 | CCTCAGCTCTCAGCC[C/T]GCAGAGCCGAATGAC | 22658 |
rs51799485 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime | Pcgf2 | Mm_Celera | 11:97700927 | AGGAGCCCTGTGAAG[G/T]CTGTCCGCCCAGTGA | 22658 |
rs212083125 | in-del | -/CGTT | | | intron-variant | Pcgf2 | Mm_Celera | 11:97691676 | CTGAGATGGCCCAGG[-/CGTT]CGTTCACCTTGTACT | 22658 |
rs212182313 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97696927 | TAGAAGGACAGAGAG[C/T]GACTGCTGAGACGCC | 22658 |
rs212266438 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97695941 | CGGTAAACAGGAGCT[C/T]CCAGTCCCCAGAGCA | 22658 |
rs212581618 | snp | A/G | | | synonymous-codon | Pcgf2 | Mm_Celera | 11:97692032 | TTGAACTTGCCTGAC[A/G]CCTTCGTAGAACTCA | 22658 |
rs212598965 | snp | C/T | | | upstream-variant-2KB | Psmb3, Pcgf2 | Mm_Celera | 11:97703119 | CACGGTAAGCGCCAG[C/T]TTACCTACTCTGCTT | 22658 |
rs212661039 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97691083 | GACCCGGCAGCTGCA[C/T]CCTGGCCACCGGGGT | 22658 |
rs212783232 | snp | A/G | | | upstream-variant-2KB | Pcgf2, Psmb3 | Mm_Celera | 11:97702276 | ATTGGGAGAAAGAAT[A/G]GTGAGAGGTGGTGAG | 22658 |
rs213045286 | in-del | -/CCGG | | | intron-variant | Pcgf2 | Mm_Celera | 11:97693046 | GAGCCAGGGTGGTGT[-/CCGG]CCCAACACAGAAGGT | 22658 |
rs213142787 | snp | C/T | | | downstream-variant-500B | Cisd3, Pcgf2 | Mm_Celera | 11:97688631 | CTCTAACTAACTGTT[C/T]CTGTGGTCACTGGCA | 22658 |
rs213199762 | in-del | -/A | | | upstream-variant-2KB, intron-variant | Pcgf2 | GRCm38.p3 | 11:97699686 | AAGAGCAGCTTGGGG[-/A]GGGGAGGGGACCAGA | 22658 |
rs213221972 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97698486 | GATCAAGCAACCACA[A/G]CAATTTTGGATAGAC | 22658 |
rs213283331 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | Pcgf2 | Mm_Celera | 11:97700270 | CGCACCTCGCGGGAA[A/G]CGCACGGTGGCCTCG | 22658 |
rs213371793 | snp | C/T | | | upstream-variant-2KB | Psmb3, Pcgf2 | Mm_Celera | 11:97703032 | CTGCAAAAATCCCGG[C/T]GAACAGTAAGGATTT | 22658 |
rs213393462 | snp | A/T | | | synonymous-codon | Pcgf2 | Mm_Celera | 11:97690290 | GCCTTCTGAGGGGGT[A/T]GGCACCGTGGGCAGG | 22658 |
rs213509512 | snp | C/T | | | upstream-variant-2KB | Pcgf2, Psmb3 | Mm_Celera | 11:97702045 | AGGTTCTTCCTCCTT[C/T]CACTCTTTTATCCCT | 22658 |
rs213664500 | in-del | -/G | | | upstream-variant-2KB, intron-variant | Pcgf2 | GRCm38.p3 | 11:97699719 | GAGGGGAGGGGCCGT[-/G]GGGGGGGGGCAAAAT | 22658 |
rs213874410 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime | Pcgf2 | Mm_Celera | 11:97700971 | AGCTCTCAGCCTGCA[G/T]AGCCGAATGACGGTG | 22658 |
rs214185885 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97698449 | AAACATATTTAAATT[C/T]ACACATACACACACC | 22658 |
rs214307783 | in-del | -/T | | | utr-variant-3-prime | Pcgf2 | Mm_Celera | 11:97689505 | TTCAACAACGGGGGG[-/T]GTGGGGGTGGGGGTT | 22658 |
rs214426176 | snp | A/G | | | missense, downstream-variant-500B | Cisd3, Pcgf2 | Mm_Celera | 11:97688374 | CCTGCAAGGCCACTC[A/G]GCGGCCCCCTTACTG | 22658 |
rs214763352 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97692225 | CTCAGAGATTGAGCC[C/T]AGTCCCCACTGGACA | 22658 |
rs215027970 | snp | A/C/T | | | intron-variant | Pcgf2 | GRCm38.p3 | 11:97692997 | TGTTGTACCTTGCCT[A/C/T]GCCTTAGGGGAGGAT | 22658 |
rs215100782 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97691223 | ACCCACTGATGGGGA[A/G]GGGGGAGGCTTCTCT | 22658 |
rs215224711 | in-del | -/ACCCACCCCA | | | utr-variant-3-prime | Pcgf2 | Mm_Celera | 11:97689204 | TGCTTGTCTGGGGCC[-/ACCCACCCCA]ACCCTCTACTCTAGG | 22658 |
rs215503229 | snp | C/T | | | upstream-variant-2KB | Psmb3, Pcgf2 | Mm_Celera | 11:97703238 | GATCCCAACATGCCC[C/T]GGACCGTAGGCTCTT | 22658 |
rs215509100 | snp | C/T | | | downstream-variant-500B | Cisd3, Pcgf2 | Mm_Celera | 11:97688757 | TAAGGTTGGGGAGCA[C/T]ACCACCGTCCTCACC | 22658 |
rs215564084 | snp | C/T | | | utr-variant-3-prime | Pcgf2 | GRCm38.p3 | 11:97689687 | GAAGAGCAGAGTGAA[C/T]TACAAAGACCCCCTA | 22658 |
rs215630156 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97690941 | TGCCCCCATCCTCTG[C/T]CACCTGCTCACAGGC | 22658 |
rs215833136 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97692203 | AGGACCTAGGGAAGT[A/G]GGGCAGCTCAGAGAT | 22658 |
rs216572820 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B | Cisd3, Pcgf2 | Mm_Celera | 11:97688622 | AGGCCTGCCCTCTAA[A/C]TAACTGTTTCTGTGG | 22658 |
rs216584772 | snp | C/T | | | upstream-variant-2KB | Pcgf2, Psmb3 | Mm_Celera | 11:97701816 | GGCATCTGTTGCCAT[C/T]GGAAACAAGAGCAAG | 22658 |
rs216597402 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97695754 | GGAGATGCTATGGAT[A/G]GAAAGGTTCCTTGTC | 22658 |
rs216604811 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97693104 | GCCAGCGGGGTAAGA[C/T]ACCTCACCAGTCCTG | 22658 |
rs216660216 | in-del | -/CCCA | | | intron-variant | Pcgf2 | Mm_Celera | 11:97693662 | GTCCACTTTTTTCCC[-/CCCA]CCGCTTCTCATATGT | 22658 |
rs216664295 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97694427 | CAGGCCCAACCTGAC[A/G]TGGTACTTTGCAGCT | 22658 |
rs216761136 | in-del | -/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | Cisd3, Pcgf2 | Mm_Celera | 11:97688970 | CAACACCCTGTCCTC[-/T]TTCCCCCCCACCCTC | 22658 |
rs216894721 | in-del | -/AAAAA | | | upstream-variant-2KB | Pcgf2, Psmb3 | Mm_Celera | 11:97702423 | GAGCATTTGCGATTT[-/AAAAA]AAAAAAAAAAAAAAA | 22658 |
rs217319006 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97694523 | CCCCACCCCCAACAG[C/T]CCACTAACTGCTCTA | 22658 |
rs217426956 | in-del | -/A | | | intron-variant | Pcgf2 | Mm_Celera | 11:97696747 | TCTGGAAGAGCAGTC[-/A]AGGGCTCTTAACCAG | 22658 |
rs217533943 | snp | C/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97697053 | ACGAGCCAGAGTATA[C/G]CATGTAGACATGAAT | 22658 |
rs217661583 | snp | A/G | | | intron-variant | Pcgf2 | GRCm38.p3 | 11:97696581 | TAGCACTTGACTAAT[A/G]AGGTGGATGGGATCT | 22658 |
rs217721672 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97696105 | GGACAGCTGGGAGAC[A/G]CAAAGCGCCTAGAGA | 22658 |
rs217723100 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97697354 | GGGTGCTCTTACCCG[C/T]TGAGCCATCTCACCA | 22658 |
rs218277749 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97694816 | TACCTCTCCTCTTTC[C/T]CCTCCTCCAGAGCAA | 22658 |
rs218619495 | snp | A/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97690528 | AGAAAGAGTGTGGGG[A/T]TGGGCGGAGACCATG | 22658 |
rs218684511 | in-del | -/TTCT | | | intron-variant | Pcgf2 | Mm_Celera | 11:97696424 | CGAACTAGACTTTTC[-/TTCT]TTCTGTAGGTATTGG | 22658 |
rs218731384 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | Pcgf2 | Mm_Celera | 11:97701166 | CGGCCCATGTGTCCC[A/G]GCATCTTGAACTCTG | 22658 |
rs218786276 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | Pcgf2 | Mm_Celera | 11:97700819 | TGGGTTGGCTCGAGT[A/G]AGGAACGAATCTTTG | 22658 |
rs218790536 | snp | C/T | | | utr-variant-3-prime | Pcgf2 | Mm_Celera | 11:97689172 | AGGGCTGTTGGCTTT[C/T]GGCAGAACTGGAGTC | 22658 |
rs218815247 | snp | A/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | Pcgf2 | Mm_Celera | 11:97699408 | GCGGGAAGGGACGCG[A/G]GCGGCAGGCCAGGCC | 22658 |
rs219124346 | in-del | -/CGGG | | | intron-variant | Pcgf2 | Mm_Celera | 11:97699130 | CCTCGGGTCGGGGGC[-/CGGG]GGAGGGGGGGGCGAG | 22658 |
rs219503508 | in-del | -/TACT | | | intron-variant | Pcgf2 | Mm_Celera | 11:97694797 | CTGGCCCGAAGGGGC[-/TACT]TACTACCTCTCCTCT | 22658 |
rs220484006 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97693917 | GGACCTGTGAGCCAG[C/T]GAGAGAACTCGGCAG | 22658 |
rs220959603 | snp | A/C | | | utr-variant-3-prime | Pcgf2 | Mm_Celera | 11:97689299 | AAATGAAGTGTTCAC[A/C]ATGCCAAAGTCACAT | 22658 |
rs221856044 | snp | C/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | Cisd3, Pcgf2 | Mm_Celera | 11:97688972 | ACACCCTGTCCTCTT[C/T]CCCCCCCACCCTCCC | 22658 |
rs221943332 | snp | A/G | | | utr-variant-5-prime, intron-variant | Pcgf2 | Mm_Celera | 11:97698024 | ACAGGATCAGGCGAC[A/G]CGACAGCCGGACTGG | 22658 |
rs221990200 | snp | C/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97691459 | CCTCCAAGGGATCCT[C/G]TGTTCAACATGGCCG | 22658 |
rs222041716 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97692426 | TCATTTCATCTAAAG[A/G]AAGGAGGCAGGAATG | 22658 |
rs222374333 | in-del | -/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97693932 | CGAGAGAACTCGGCA[-/G]GTAAAGGAAGACTCA | 22658 |
rs222503861 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97698751 | CGTTCTTTCCCCTCC[A/G]CCCTTGCTTCCCCGC | 22658 |
rs222887990 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97696446 | AGGTATTGGTTTCTG[A/G]TACCACAGAGAGCGG | 22658 |
rs223067492 | snp | C/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97691248 | TTCTCTTTCTAGGAC[C/G]GCTTTGACCCAGGCT | 22658 |
rs223256159 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97695660 | TAAGAAGCCACAGGA[A/G]CCCCACACAGTCTGT | 22658 |
rs223385031 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97694288 | GGCCTCAGAACACTG[C/T]CTTCCTCTAATGTCT | 22658 |
rs223499485 | in-del | -/CA | | | intron-variant | Pcgf2 | Mm_Celera | 11:97693269 | CCATCATCACCACAC[-/CA]CACACACACACACAC | 22658 |
rs223509923 | snp | C/T | | | utr-variant-3-prime | Pcgf2 | Mm_Celera | 11:97689314 | CATGCCAAAGTCACA[C/T]ATAGACTTTATAGGG | 22658 |
rs223576233 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97690595 | CGCCCCTATTGCTGA[C/T]CCCGAATCTGAATCT | 22658 |
rs223695156 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97694822 | TCCTCTTTCTCCTCC[C/T]CCAGAGCAAAAGCCC | 22658 |
rs223765852 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97693976 | ACGGTGGAAAGAGAG[A/G]AAACCATGCCTGCAA | 22658 |
rs224119785 | snp | A/C | | | upstream-variant-2KB | Pcgf2, Psmb3 | Mm_Celera | 11:97702443 | AAAAAAAAAAAAGGC[A/C]GAGACCGTCCCTGGG | 22658 |
rs224328472 | snp | A/T | | | upstream-variant-2KB | Pcgf2, Psmb3 | Mm_Celera | 11:97701463 | TTTAGGCACAGTAGG[A/T]AAGCTGGGCTTTGAC | 22658 |
rs225040728 | snp | A/C | | | intron-variant | Pcgf2 | Mm_Celera | 11:97696939 | GAGCGACTGCTGAGA[A/C]GCCCATCCTGTGGGC | 22658 |
rs225046790 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97698253 | GTTTCGGGAACAGCA[C/T]AACTGCAAGAAGTCC | 22658 |
rs225166531 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97693638 | GTGCTCCCCTCCCCC[C/T]GGGCCCAAAGTCCAC | 22658 |
rs225337917 | in-del | -/AC | | | upstream-variant-2KB, intron-variant | Pcgf2 | Mm_Celera | 11:97700203 | CTAAGTGCGTGTGTG[-/AC]ATCCCCCCCCGAGCG | 22658 |
rs225375819 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97692575 | CTGGGAAAGATTATA[C/T]AGGAGCATTAGCAAC | 22658 |
rs225511665 | in-del | -/CCGCCCA | | | intron-variant | Pcgf2 | Mm_Celera | 11:97691825 | CATTCATGGCACTCT[-/CCGCCCA]CAGCCCACAGCTAGA | 22658 |
rs226229803 | snp | A/G | | | upstream-variant-2KB | Pcgf2, Psmb3 | Mm_Celera | 11:97701607 | AAATGTCTAGAGAAC[A/G]GATGGAAAGAGTCCC | 22658 |
rs226237985 | snp | A/T | | | upstream-variant-2KB | Psmb3, Pcgf2 | Mm_Celera | 11:97703060 | TTTGTGAATGAACAC[A/T]GGAAGTCGGGTAGCT | 22658 |
rs226373457 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97697862 | GTCCGGGGTGGGGGT[A/G]GGGGGGCGCTACAGT | 22658 |
rs226695610 | in-del | -/G | | | upstream-variant-2KB, utr-variant-5-prime | Pcgf2 | Mm_Celera | 11:97700733 | TACTTATGATTTATT[-/G]GGGGGTGGCCACTGT | 22658 |
rs226886007 | snp | G/T | | | missense | Pcgf2 | Mm_Celera | 11:97693443 | ATTCCACAATGGTGG[G/T]GGCATCAATAAAATA | 22658 |
rs226926219 | in-del | -/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97697191 | TCTTTTCTTTCTTTC[-/T]TTTTTTTTTATTATT | 22658 |
rs227065029 | in-del | -/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97692469 | CTGGGAAGTGGGGGT[-/G]GGGGGAGCAGGGACA | 22658 |
rs227992207 | snp | G/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97692618 | ATCTCGCTAGCCGGG[G/T]ATCAGCTCTGTACCC | 22658 |
rs228181874 | in-del | -/AAA | | | utr-variant-5-prime, intron-variant | Pcgf2 | Mm_Celera | 11:97699318 | GGAAGGGAGGAAAGG[-/AAA]AAAAAAAAAGAGAGA | 22658 |
rs228214953 | in-del | -/GGG | | | utr-variant-3-prime | Pcgf2 | Mm_Celera | 11:97689367 | GGATGGAGGGTTGGG[-/GGG]GGGGGGGCTTCCACT | 22658 |
rs228360642 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97692160 | GAGACAGCTCAGAGG[A/G]GTTGGTCAAAGATAG | 22658 |
rs228368301 | snp | A/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97692709 | CGAGGAGGCAGGGTA[A/T]GGGGTCTGAAGCCCA | 22658 |
rs228622553 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97690708 | GACTGCTCTGAATTC[A/G]AGGCCAGCCTGGACT | 22658 |
rs228694015 | snp | A/G | | | synonymous-codon | Pcgf2 | Mm_Celera | 11:97691873 | CTTCTCCTTGTCCCC[A/G]TCTCCATTCTCCGTG | 22658 |
rs228755663 | snp | C/T | | | upstream-variant-2KB | Psmb3, Pcgf2 | Mm_Celera | 11:97702712 | AGGGAAAGCAAGGGA[C/T]GCACACGTCCCACCT | 22658 |
rs229112746 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97695725 | CACTTTCTAAGCCCA[A/G]GGCCCTAAGGGAAGG | 22658 |
rs229124231 | snp | A/C | | | intron-variant | Pcgf2 | Mm_Celera | 11:97696634 | CCCTTCTCTCTCTTG[A/C]TCAGGCCCATAGTTT | 22658 |
rs229854616 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97693012 | AGCCTTAGGGGAGGA[C/T]GGGCCCCTCTATCTC | 22658 |
rs229870166 | snp | G/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97696896 | TCGGACTCAGCGGAA[G/T]AGCTGAGCAGGTGGG | 22658 |
rs229943778 | in-del | -/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97697016 | TACAGATGGGGAAAC[-/T]TAGGGCACAATGGAA | 22658 |
rs229951238 | in-del | -/CC | | | intron-variant | Pcgf2 | Mm_Celera | 11:97693659 | AAAGTCCACTTTTTT[-/CC]CCCCCGCTTCTCATA | 22658 |
rs230307368 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97695777 | TCCTTGTCTCCCCTA[A/G]GAGTAAAGAGCCTCC | 22658 |
rs230381337 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97697617 | GTCATGCACACAGGC[C/T]AGACAGACACTTGGC | 22658 |
rs230437548 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97698514 | GACCCGGGAAGTGAG[A/G]GATGGAAGAGTAGGG | 22658 |
rs230638994 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97691048 | GATCTCCACCTGGAG[A/G]GAGGGGATGACACCC | 22658 |
rs230903676 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97695959 | AGTCCCCAGAGCATC[C/T]ATCCCCTCCCCACTT | 22658 |
rs231018004 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97694817 | ACCTCTCCTCTTTCT[C/T]CTCCTCCAGAGCAAA | 22658 |
rs231043353 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Cisd3, Pcgf2 | Mm_Celera | 11:97688486 | TAATGCTGAGCCACA[C/T]ATGGAAGGGAACCTC | 22658 |
rs231177737 | snp | A/G | | | upstream-variant-2KB, intron-variant | Pcgf2 | Mm_Celera | 11:97700185 | GCTGAATCCCTTGGG[A/G]TTCCTAAGTGCGTGT | 22658 |
rs231245157 | snp | C/G | | | utr-variant-3-prime | Pcgf2 | Mm_Celera | 11:97689368 | GGATGGAGGGTTGGG[C/G]GGGGGGCTTCCACTG | 22658 |
rs231786965 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97698289 | GGGAGGCCCAAGACT[A/G]TGAGAGCCAGCTAAG | 22658 |
rs232070645 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97694201 | CACCAATGAGAGATT[C/T]TTCATGGCGAAACCT | 22658 |
rs232200012 | snp | A/G | | | upstream-variant-2KB, intron-variant | Pcgf2 | GRCm38.p3 | 11:97699654 | GGGGAGAAACCTATG[A/G]TAAGAAAGGAGTTTG | 22658 |
rs232440754 | in-del | -/AAAT | | | intron-variant | Pcgf2 | Mm_Celera | 11:97697465 | AGTTCCTGAAAACAG[-/AAAT]AAATAAATAAATAAA | 22658 |
rs232540634 | snp | G/T | | | upstream-variant-2KB | Pcgf2, Psmb3 | Mm_Celera | 11:97702113 | TCCACCGGGACAGAT[G/T]TCCTCTTTCAAGTTG | 22658 |
rs232575061 | snp | C/T | | | downstream-variant-500B | Cisd3, Pcgf2 | Mm_Celera | 11:97688759 | AGGTTGGGGAGCATA[C/T]CACCGTCCTCACCGT | 22658 |
rs232653638 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | Pcgf2 | Mm_Celera | 11:97700983 | GCAGAGCCGAATGAC[A/G]GTGTAAAGGAAAGGC | 22658 |
rs232677437 | snp | A/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97691535 | ACTATTTGCATGCAC[A/T]CATCCTTGTCCCTAG | 22658 |
rs232786994 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97692889 | AACACTCAGCTCTCT[C/T]TTCCCACCATGACCC | 22658 |
rs232926442 | snp | A/C | | | utr-variant-3-prime | Pcgf2 | Mm_Celera | 11:97689624 | GGACATAGGGAAGGA[A/C]ATTAATACTTCCAAT | 22658 |
rs233344485 | in-del | -/GGT | | | utr-variant-3-prime | Pcgf2 | Mm_Celera | 11:97689503 | CATTCAACAACGGGG[-/GGT]GGGTGGGGGTGGGGG | 22658 |
rs233416523 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97690862 | GAGTGTCTGACATAA[A/G]AGGGTGCCTCATGTC | 22658 |
rs233526072 | snp | C/G | | | upstream-variant-2KB | Psmb3, Pcgf2 | Mm_Celera | 11:97702984 | AAGAATGGGCGCCTT[C/G]GGTATACTCGGTGCC | 22658 |
rs233685105 | in-del | -/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97696565 | TTCAAGGTCACATCC[-/T]TAGCACTTGACTAAT | 22658 |
rs233878373 | snp | C/T | | | utr-variant-3-prime | Pcgf2 | Mm_Celera | 11:97689985 | GGAGAGGGTCCCTTT[C/T]CTCAAGGGGGGCAAG | 22658 |
rs234093036 | in-del | -/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97696682 | TTGTTTGTTTGTTTG[-/T]TTTTGTTTCTCATTA | 22658 |
rs234637106 | snp | A/G | | | downstream-variant-500B | Cisd3, Pcgf2 | Mm_Celera | 11:97688687 | ATGATCTGTGGAGGC[A/G]GAGGGTGTCTGGTGA | 22658 |
rs234858903 | in-del | -/AAA | | | intron-variant | Pcgf2 | Mm_Celera | 11:97696859 | CCCAAGGTCACTCAG[-/AAA]AAAAAAAAACGGGCG | 22658 |
rs234946607 | in-del | -/A | | | utr-variant-3-prime | Pcgf2 | Mm_Celera | 11:97689364 | TAGGGATGGAGGGTT[-/A]GGGGGGGGGGCTTCC | 22658 |
rs235140791 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97694448 | CTTTGCAGCTAATTC[A/G]AGGGCCTGGCAGAAA | 22658 |
rs235370299 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97691094 | TGCACCCTGGCCACC[A/G]GGGTTGGGAGTCTTG | 22658 |
rs235425472 | snp | C/T | | | upstream-variant-2KB | Pcgf2, Psmb3 | Mm_Celera | 11:97702324 | TCCATTCACTGACCA[C/T]AGACGGATTTCTAAA | 22658 |
rs235436349 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97690533 | GAGTGTGGGGTTGGG[C/T]GGAGACCATGCAGTT | 22658 |
rs236024191 | snp | A/T | | | upstream-variant-2KB | Pcgf2, Psmb3 | Mm_Celera | 11:97701662 | TTCTCCAGTGTGCTC[A/T]GCGAACATGAAGAGC | 22658 |
rs236089472 | snp | A/C | | | upstream-variant-2KB | Psmb3, Pcgf2 | Mm_Celera | 11:97702692 | AACAGTGGTTGTGCA[A/C]GGGAAGGGAAAGCAA | 22658 |
rs236225980 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97692239 | CCAGTCCCCACTGGA[C/T]AGTACTGTAGCTGGG | 22658 |
rs236276325 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97694548 | GCTCTAGTGTGCAGG[A/G]TCTAGGGACCCACTC | 22658 |
rs236496503 | snp | A/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97696610 | CTTTTAAAAAATTCT[A/T]TCCCCCTTCCCTTCT | 22658 |
rs236591862 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97695690 | TCATTTTAGAGGTTT[C/T]ATCCGAGAGAAGCCC | 22658 |
rs236794004 | snp | A/G | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | Cisd3, Pcgf2 | Mm_Celera | 11:97688992 | CCCACCCTCCCCCCA[A/G]ATCTATGTACACTTG | 22658 |
rs236818218 | in-del | -/CAAA | | | intron-variant | Pcgf2 | Mm_Celera | 11:97690761 | AGGGAATGACTGTCT[-/CAAA]CAAACAAACAAACAA | 22658 |
rs236885770 | in-del | -/A | | | intron-variant | Pcgf2 | Mm_Celera | 11:97696820 | CTCAATTTACAGATG[-/A]AAAAAAAACTTAGAT | 22658 |
rs237414600 | in-del | -/GTGCCCCCAAGCT | | | intron-variant | Pcgf2 | Mm_Celera | 11:97693379 | CATTTTCCCTGAGCA[-/GTGCCCCCAAGCT]GTGCCCCCAAGCTGG | 22658 |
rs237450661 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97697230 | CTATGTAAGTACACT[A/G]TAGCTGTCTTCAGAC | 22658 |
rs237686386 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97698648 | GAGTAGCCGCTTCCC[C/T]TTTCGCCTCCTGTGG | 22658 |
rs238150015 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97696193 | TGGTGTCAATGGAGC[C/T]GGGGAAGAACCCAGT | 22658 |
rs238294755 | snp | A/C | | | intron-variant | Pcgf2 | Mm_Celera | 11:97693944 | GCAGGTAAAGGAAGA[A/C]TCAAGCCTGGTGACA | 22658 |
rs238345297 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97693777 | TTCCACCTTGAGAAG[C/T]AAGGTCATATACCAT | 22658 |
rs238483791 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97692619 | TCTCGCTAGCCGGGG[A/G]TCAGCTCTGTACCCC | 22658 |
rs238684794 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97690427 | ACGGACCAGGGGTGA[C/T]CCTATCCCTATACCC | 22658 |
rs239157615 | in-del | -/C | | | upstream-variant-2KB, intron-variant | Pcgf2 | Mm_Celera | 11:97699903 | GAGACCACCTCTTAT[-/C]CAAGCAGATCCCTTG | 22658 |
rs239297429 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97698459 | AAATTTACACATACA[C/T]ACACCCTTCTCGATC | 22658 |
rs239381543 | snp | G/T | | | upstream-variant-2KB | Psmb3, Pcgf2 | Mm_Celera | 11:97703133 | GCTTACCTACTCTGC[G/T]TACAGCACCAGCCCC | 22658 |
rs239536621 | in-del | -/GTGGGGGT | | | utr-variant-3-prime | Pcgf2 | Mm_Celera | 11:97689369 | ATGGAGGGTTGGGGG[-/GTGGGGGT]GGGGGCTTCCACTGT | 22658 |
rs239536870 | snp | A/C | | | intron-variant | Pcgf2 | Mm_Celera | 11:97698966 | CCGACCCCAGGAGTT[A/C]GGGCGCCCTCCCTCG | 22658 |
rs240327114 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97697137 | TCATGTGTTCATGTA[C/T]GAGTCAGAGGGGTTC | 22658 |
rs240858891 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97691225 | CCACTGATGGGGAGG[A/G]GGGAGGCTTCTCTTT | 22658 |
rs240924048 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97694862 | GAGAGGCTGGCCAAG[C/T]CCCAACCACTCCTTT | 22658 |
rs241310060 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97691340 | GAACATGTGACCTGA[C/T]GGATGAGCGCCACAG | 22658 |
rs241522105 | in-del | -/AA | | | intron-variant | Pcgf2 | Mm_Celera | 11:97697659 | CACCACATACACAGC[-/AA]GGCTGGAGCCAGGCT | 22658 |
rs241627385 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97692438 | AAGAAAGGAGGCAGG[A/G]ATGAGTGGGCGACAG | 22658 |
rs241738472 | in-del | -/GTC | | | upstream-variant-2KB, utr-variant-5-prime | Pcgf2 | Mm_Celera | 11:97700833 | AAGGAACGAATCTTT[-/GTC]GTCGAGCCTGCCTCC | 22658 |
rs241761431 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97691473 | TCTGTTCAACATGGC[C/T]GACCAGCCCGTATCC | 22658 |
rs241879412 | snp | A/T | | | utr-variant-3-prime | Pcgf2 | Mm_Celera | 11:97689229 | TCTAGGCCCCCAGTG[A/T]GTGTCACCTCCAGTC | 22658 |
rs242007449 | snp | A/G | | | upstream-variant-2KB | Pcgf2 | Mm_Celera | 11:97701385 | TCCCTGTGGTTCATC[A/G]GGAGAGCCGCTGACT | 22658 |
rs242090270 | snp | G/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | Pcgf2 | Mm_Celera | 11:97699411 | GGAAGGGACGCGGGC[G/T]GCAGGCCAGGCCGGG | 22658 |
rs242485194 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97694026 | CGCATGCGCGTGCTC[A/G]CACACAGAAAATAAA | 22658 |
rs242543235 | snp | A/C | | | upstream-variant-2KB, intron-variant | Pcgf2 | Mm_Celera | 11:97700237 | CCTCACCGCCTCCCC[A/C]CACCGATTCGGGGTC | 22658 |
rs242686968 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97695406 | GCTGTCTGGGCTTCT[A/G]AAGGTACTCCATGTG | 22658 |
rs242765314 | in-del | -/AAAA | | | upstream-variant-2KB | Pcgf2, Psmb3 | Mm_Celera | 11:97702424 | GAGCATTTGCGATTT[-/AAAA]AAAAAAAAAAAAGGC | 22658 |
rs242916496 | snp | A/C | | | intron-variant | Pcgf2 | Mm_Celera | 11:97694312 | AATGTCTCTGGATGC[A/C]GACAGCTCCTTGAAC | 22658 |
rs243089687 | snp | A/G | | | intron-variant | Pcgf2 | GRCm38.p3 | 11:97693048 | GCCAGGGTGGTGTCC[A/G]GCCCAACACAGAAGG | 22658 |
rs243171635 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97691072 | GACACCCATGGGACC[C/T]GGCAGCTGCACCCTG | 22658 |
rs243357743 | snp | C/T | | | upstream-variant-2KB | Psmb3, Pcgf2 | Mm_Celera | 11:97703116 | CACCACGGTAAGCGC[C/T]AGCTTACCTACTCTG | 22658 |
rs243502126 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97692578 | GGAAAGATTATACAG[A/G]AGCATTAGCAACCAC | 22658 |
rs244056499 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97690615 | AATCTGAATCTGAGT[A/G]GTAGCAACCAGGGCA | 22658 |
rs244529167 | snp | G/T | | | utr-variant-3-prime | Pcgf2 | Mm_Celera | 11:97689511 | CAACGGGGGGGTGGG[G/T]GTGGGGGTTTGGACA | 22658 |
rs244600090 | snp | C/T | | | synonymous-codon | Pcgf2 | Mm_Celera | 11:97691876 | CTCCTTGTCCCCATC[C/T]CCATTCTCCGTGAGG | 22658 |
rs245002563 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97696717 | TGGCTGGCTGCTGGG[A/G]TTTGAACTCATGACC | 22658 |
rs245046386 | in-del | -/AC | | | utr-variant-3-prime | Pcgf2 | Mm_Celera | 11:97689441 | CCTCACTGCCAGAGG[-/AC]ACAGACTGCATTTGT | 22658 |
rs245121606 | in-del | -/G | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | Cisd3, Pcgf2 | Mm_Celera | 11:97689064 | CCACCAGGTAGAGTT[-/G]GGGGTCAGCTCATTC | 22658 |
rs245201177 | in-del | -/TACT | | | upstream-variant-2KB | Pcgf2, Psmb3 | Mm_Celera | 11:97701984 | ATCTTCCGCACTGTC[-/TACT]TACTTAGGCCCCCTC | 22658 |
rs245597806 | in-del | -/AACAAACG | | | intron-variant | Pcgf2 | Mm_Celera | 11:97690787 | ACAAACAAACAAACA[-/AACAAACG]AACGAACGAAATGGC | 22658 |
rs245602986 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97696466 | ACAGAGAGCGGGTCC[C/T]GCAGCCTCCAGGGAC | 22658 |
rs245640131 | in-del | -/T | | | upstream-variant-2KB, utr-variant-5-prime | Pcgf2 | Mm_Celera | 11:97701229 | TACTGCCTGGCTACC[-/T]TTTGTTTATTGGGGT | 22658 |
rs246228327 | snp | A/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97691630 | CCTGCAGGCCCAGCT[A/T]TCCAACTCTGTGATG | 22658 |
rs246434471 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97690581 | CGTTCCACTGTAGCC[A/G]CCCCTATTGCTGACC | 22658 |
rs246543337 | snp | A/G | | | upstream-variant-2KB | Psmb3, Pcgf2 | Mm_Celera | 11:97702524 | TGCGCCACAGAGACG[A/G]TGACAGTTGTTTGTG | 22658 |
rs247382693 | in-del | -/AAAA | | | intron-variant | Pcgf2 | Mm_Celera | 11:97696858 | CCCAAGGTCACTCAG[-/AAAA]AAAAAAAAAAAACGG | 22658 |
rs247674491 | snp | C/T | | | utr-variant-3-prime | Pcgf2 | GRCm38.p3 | 11:97689666 | ACCACCAGATACACC[C/T]CCCAAGAAGAGCAGA | 22658 |
rs247679454 | snp | A/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97697878 | GGGGGGCGCTACAGT[A/T]GGCATCTGACCTGTA | 22658 |
rs247724375 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97690753 | AGGCCAGCCAGGGAA[C/T]GACTGTCTCAAACAA | 22658 |
rs247829280 | snp | C/G | | | downstream-variant-500B | Cisd3, Pcgf2 | Mm_Celera | 11:97688739 | CCACTCCAGTTAGCA[C/G]TGTAAGGTTGGGGAG | 22658 |
rs248047940 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97698274 | CAAGAAGTCCAGAGA[A/G]GGAGGCCCAAGACTG | 22658 |
rs248191416 | in-del | -/GTTTGTTTGTTTGTTTGTTT | | | intron-variant | Pcgf2 | Mm_Celera | 11:97696646 | TTGCTCAGGCCCATA[-/GTTTGTTTGTTTGTTTGTTT]GTTTGTTTGTTTGTT | 22658 |
rs248219604 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97697048 | CCAGAACGAGCCAGA[A/G]TATAGCATGTAGACA | 22658 |
rs248432831 | snp | A/G | | | synonymous-codon | Pcgf2 | Mm_Celera | 11:97692752 | CAGTGGTCGAGTTTT[A/G]TGGACCTGGACGTCA | 22658 |
rs248512596 | snp | C/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97697353 | CGGGTGCTCTTACCC[C/G]TTGAGCCATCTCACC | 22658 |
rs248616356 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97692177 | TTGGTCAAAGATAGA[A/G]CAAGGGACTGAGGAC | 22658 |
rs248878782 | snp | C/T | | | synonymous-codon | Pcgf2 | Mm_Celera | 11:97692415 | CCGTCGCCGTTTCAT[C/T]TCATCTAAAGAAAGG | 22658 |
rs248966334 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97691366 | CACAGCACTTACTGT[C/T]TCCCTACCCAAGTAT | 22658 |
rs249135198 | snp | A/G | | | upstream-variant-2KB | Pcgf2, Psmb3 | Mm_Celera | 11:97701534 | CTTCTCCATGTTTGA[A/G]GCGCCAGGTGATCTG | 22658 |
rs249306763 | snp | C/T | | | utr-variant-3-prime | Pcgf2 | Mm_Celera | 11:97689417 | ATGCCTTCTTCACAG[C/T]CACTTGGTCCTCACT | 22658 |
rs249452707 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | Pcgf2 | Mm_Celera | 11:97701118 | AGGCTACTGTGGAAA[C/G]GGGTCTCGAGTTAGA | 22658 |
rs249819336 | in-del | -/AAG | | | utr-variant-5-prime, intron-variant | Pcgf2 | Mm_Celera | 11:97699326 | GGAAAGGAAAAAAAA[-/AAG]AGAGAGAGAGACCGG | 22658 |
rs250148093 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97696580 | CTAGCACTTGACTAA[C/T]GAGGTGGATGGGATC | 22658 |
rs250460581 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97692978 | CGCATCCACACATCT[A/G]GGCTGTTGTACCTTG | 22658 |
rs251051101 | snp | C/T | | | upstream-variant-2KB | Psmb3, Pcgf2 | Mm_Celera | 11:97703016 | ATAGGTTAATTGGCG[C/T]CTGCAAAAATCCCGG | 22658 |
rs251111156 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97690902 | ACTGACCAATGCCAG[A/G]CCTGGCCAGGCAGGA | 22658 |
rs251398629 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97692478 | GGGGGTGGGGGGAGC[A/G]GGGACAACACAGGGG | 22658 |
rs251506322 | in-del | -/CCACACC | | | intron-variant | Pcgf2 | Mm_Celera | 11:97693263 | GACTCCCCATCATCA[-/CCACACC]ACACACACACACACA | 22658 |
rs251557611 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97695819 | TCGCATCCCTAGGGG[C/T]CTCAGAAAGCCACCA | 22658 |
rs251676920 | in-del | -/CAGCT | | | intron-variant | Pcgf2 | Mm_Celera | 11:97697104 | CCGGCATCATAGACC[-/CAGCT]CTGCAAGCAAATCTC | 22658 |
rs251688518 | snp | C/G | | | upstream-variant-2KB | Psmb3, Pcgf2 | Mm_Celera | 11:97702763 | GCCCAGGCTATCCTC[C/G]GTCAGTGTCTAGGAT | 22658 |
rs252078381 | in-del | -/AG | | | intron-variant | Pcgf2 | Mm_Celera | 11:97697862 | GTCCGGGGTGGGGGT[-/AG]GGGGGCGCTACAGTA | 22658 |
rs252225007 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97694474 | AGAAAGACCTCTCCT[A/G]TCCTGTAGTGGGAAC | 22658 |
rs252349339 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97698551 | CCTAGACGCCCCTGG[A/G]AGTCAGGAAGGGCGC | 22658 |
rs252465937 | snp | A/C | | | intron-variant | Pcgf2 | Mm_Celera | 11:97697810 | AGTCTTCCAGCAACA[A/C]AGACAGGTCAGCGCC | 22658 |
rs252786868 | in-del | -/A | | | intron-variant | Pcgf2 | Mm_Celera | 11:97693268 | CCATCATCACCACAC[-/A]CACACACACACACAC | 22658 |
rs252912949 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | Cisd3, Pcgf2 | Mm_Celera | 11:97688613 | TAAACACTGAGGCCT[A/G]CCCTCTAACTAACTG | 22658 |
rs252988745 | in-del | -/GA | | | upstream-variant-2KB, intron-variant | Pcgf2 | GRCm38.p3 | 11:97699728 | GGCCGTGGGGGGGGG[-/GA]CAAAATGGCTTTTTT | 22658 |
rs253371489 | snp | A/G | | | upstream-variant-2KB, intron-variant | Pcgf2 | Mm_Celera | 11:97699918 | CCAAGCAGATCCCTT[A/G]AACCCGGAGGAAAGG | 22658 |
rs253766076 | in-del | -/AGCTGGTACATTCAC | | | intron-variant | Pcgf2 | Mm_Celera | 11:97692290 | GACAGTGTGGGCCAA[-/AGCTGGTACATTCAC]AGCTGGGGCAGCCCT | 22658 |
rs254217885 | in-del | -/G | | | utr-variant-3-prime | Pcgf2 | Mm_Celera | 11:97689500 | TGAACATTCAACAAC[-/G]GGGGGGTGGGGGTGG | 22658 |
rs254380056 | in-del | -/C | | | intron-variant | Pcgf2 | Mm_Celera | 11:97693660 | AAAGTCCACTTTTTT[-/C]CCCCGCTTCTCATAT | 22658 |
rs254423683 | in-del | -/AA | | | intron-variant | Pcgf2 | Mm_Celera | 11:97698629 | GCAGAGCTCAAGGAG[-/AA]AAGAGTAGCCGCTTC | 22658 |
rs254587727 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97696043 | GGGGCTGAGGTGCTG[A/G]TGGGGAGGACAAGGA | 22658 |
rs254621797 | snp | C/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | Cisd3, Pcgf2 | Mm_Celera | 11:97689079 | TGGGGTCAGCTCATT[C/T]TTTTATTTTCTTGTG | 22658 |
rs254682112 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97694821 | CTCCTCTTTCTCCTC[C/T]TCCAGAGCAAAAGCC | 22658 |
rs254775706 | snp | A/T | | | upstream-variant-2KB | Psmb3, Pcgf2 | Mm_Celera | 11:97702711 | AAGGGAAAGCAAGGG[A/T]TGCACACGTCCCACC | 22658 |
rs254820245 | in-del | -/ACCT | | | intron-variant | Pcgf2 | Mm_Celera | 11:97697439 | AAGATAGAAGCCTCG[-/ACCT]ACCTACCACTCAGTT | 22658 |
rs254903840 | snp | A/C | | | upstream-variant-2KB | Pcgf2, Psmb3 | Mm_Celera | 11:97701677 | AGCGAACATGAAGAG[A/C]GCTTATTTTCCACCA | 22658 |
rs255006610 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97694243 | ACTGGGACACAGGCC[C/T]ACCACCTGTCCCTTT | 22658 |
rs255018440 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97691207 | CCAAGAAACTCCCCT[A/G]ACCCACTGATGGGGA | 22658 |
rs255113295 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97690564 | ATGGAAGGAAGGTAT[C/T]ACGTTCCACTGTAGC | 22658 |
rs255131381 | snp | A/G | | | upstream-variant-2KB | Pcgf2, Psmb3 | Mm_Celera | 11:97701767 | AGAGGTTCCCAGAGA[A/G]CAGGAACCCAGAACA | 22658 |
rs255408644 | in-del | -/GG | | | intron-variant | Pcgf2 | Mm_Celera | 11:97699133 | CGGGTCGGGGGCGGA[-/GG]GGGGGGGGCGAGACC | 22658 |
rs255700001 | snp | A/G | | | synonymous-codon | Pcgf2 | Mm_Celera | 11:97690002 | TCAAGGGGGGCAAGG[A/G]GCGCCATTAACAGTC | 22658 |
rs255996031 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97698226 | TTGGGGGTGGGGGTG[A/G]GGTTGTCATGAGTTT | 22658 |
rs256008069 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97698993 | CTCGGCCACCAGAAA[A/G]CCAAGTCCCCTTCCT | 22658 |
rs256221332 | snp | A/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97696897 | CGGACTCAGCGGAAG[A/T]GCTGAGCAGGTGGGT | 22658 |
rs256508153 | in-del | -/AC | | | intron-variant | Pcgf2 | Mm_Celera | 11:97696134 | AAGAAAAAGTGAAAG[-/AC]ACAGTTCCCAAGAAG | 22658 |
rs257061867 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97691239 | GGGGGAGGCTTCTCT[C/T]TCTAGGACCGCTTTG | 22658 |
rs257281788 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97695753 | AGGAGATGCTATGGA[C/T]GGAAAGGTTCCTTGT | 22658 |
rs257320640 | in-del | -/CCA | | | intron-variant | Pcgf2 | Mm_Celera | 11:97697826 | AGACAGGTCAGCGCC[-/CCA]CCACCACTCCGCTAT | 22658 |
rs257410119 | snp | A/C | | | intron-variant | Pcgf2 | Mm_Celera | 11:97691490 | ACCAGCCCGTATCCT[A/C]GAGTTCCTTGGCCCT | 22658 |
rs257569461 | snp | A/C | | | intron-variant | Pcgf2 | Mm_Celera | 11:97690839 | CCTGGCTCCAGAGAC[A/C]AGGGATGGAGTGTCT | 22658 |
rs257811801 | snp | C/T | | | upstream-variant-2KB | Pcgf2, Psmb3 | Mm_Celera | 11:97701880 | GAGAGAGTCGTTCCT[C/T]CTTGCTTTTGTGTAG | 22658 |
rs258585503 | in-del | -/A | | | intron-variant | Pcgf2 | Mm_Celera | 11:97696022 | CCTGATGCAGGGGGT[-/A]GGGTGGGGGCTGAGG | 22658 |
rs258717813 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97696611 | TTTTAAAAAATTCTT[C/T]CCCCCTTCCCTTCTC | 22658 |
rs258861816 | in-del | -/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97697019 | AGATGGGGAAACTTA[-/G]GGCACAATGGAAACC | 22658 |
rs258879572 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97695691 | CATTTTAGAGGTTTC[A/G]TCCGAGAGAAGCCCC | 22658 |
rs259064289 | snp | C/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | Cisd3, Pcgf2 | Mm_Celera | 11:97688971 | AACACCCTGTCCTCT[C/T]TCCCCCCCACCCTCC | 22658 |
rs259481537 | in-del | -/AAGGTTCCTTGTCTCCCCT | | | intron-variant | Pcgf2 | Mm_Celera | 11:97695757 | GATGCTATGGATGGA[-/AAGGTTCCTTGTCTCCCCT]AAGAGTAAAGAGCCT | 22658 |
rs259699855 | snp | A/C | | | intron-variant | Pcgf2 | Mm_Celera | 11:97697165 | TTCTGCACCAGGACA[A/C]AAAATCTCTTATCTT | 22658 |
rs259826527 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97694870 | GGCCAAGCCCCAACC[A/G]CTCCTTTACAACACA | 22658 |
rs259969525 | in-del | -/TG | | | intron-variant | Pcgf2 | Mm_Celera | 11:97691639 | CCAGCTATCCAACTC[-/TG]TGATGGCTGACAGAG | 22658 |
rs259988744 | snp | C/G | | | upstream-variant-2KB | Psmb3, Pcgf2 | Mm_Celera | 11:97703136 | TACCTACTCTGCTTA[C/G]AGCACCAGCCCCACA | 22658 |
rs260934106 | snp | A/C | | | intron-variant | Pcgf2 | Mm_Celera | 11:97692657 | TTCAGACCCAGCATT[A/C]AGGCATGCAGGCTCC | 22658 |
rs260943861 | snp | A/C/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97693959 | CTCAAGCCTGGTGAC[A/C/G]CACGGTGGAAAGAGA | 22658 |
rs261102608 | in-del | -/TA | | | utr-variant-3-prime | Pcgf2 | Mm_Celera | 11:97689844 | GTACATATATATATT[-/TA]TATATATATATAGAT | 22658 |
rs261252417 | snp | C/T | | | utr-variant-3-prime | Pcgf2 | Mm_Celera | 11:97689261 | TGCTAGATTGCGTTC[C/T]TGGGTTGGGGTAGGA | 22658 |
rs261402762 | in-del | -/A | | | utr-variant-3-prime, downstream-variant-500B | Cisd3, Pcgf2 | Mm_Celera | 11:97688599 | GGTAAAGCTGTCAAT[-/A]AACACTGAGGCCTGC | 22658 |
rs261416502 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97698276 | AGAAGTCCAGAGAGG[A/G]AGGCCCAAGACTGTG | 22658 |
rs261926890 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97692221 | GCAGCTCAGAGATTG[A/G]GCCCAGTCCCCACTG | 22658 |
rs262076146 | snp | G/T | | | upstream-variant-2KB | Psmb3, Pcgf2 | Mm_Celera | 11:97702562 | GAGCCGAGTCAATAG[G/T]ACTGAGCCGATATGG | 22658 |
rs262326726 | snp | G/T | | | utr-variant-3-prime | Pcgf2 | Mm_Celera | 11:97689513 | ACGGGGGGGTGGGGG[G/T]GGGGGTTTGGACAGG | 22658 |
rs262422185 | snp | A/G | | | utr-variant-3-prime | Pcgf2 | Mm_Celera | 11:97689365 | TAGGGATGGAGGGTT[A/G]GGGGGGGGGCTTCCA | 22658 |
rs262470704 | snp | A/G | | | upstream-variant-2KB | Pcgf2, Psmb3 | Mm_Celera | 11:97701545 | TTGAAGCGCCAGGTG[A/G]TCTGCAAACATAGAA | 22658 |
rs262550436 | snp | A/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97694610 | ACTGGGATCCCACCA[A/T]GTCCCAACCTGGTGA | 22658 |
rs262663710 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97694271 | TTTGACTGTCCCACT[C/T]GGGCCTCAGAACACT | 22658 |
rs262776375 | in-del | -/TATG | | | intron-variant | Pcgf2 | Mm_Celera | 11:97697216 | ATTATTTATTTATTC[-/TATG]TAAGTACACTGTAGC | 22658 |
rs262923271 | snp | G/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97693394 | AGTGCCCCCAAGCTG[G/T]GCACCCCCGAATTCA | 22658 |
rs262966012 | snp | C/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97691851 | CTAGACAGGCCCTAA[C/G]ACTCACCTTCTCCTT | 22658 |
rs263074215 | snp | C/T | | | synonymous-codon | Pcgf2 | Mm_Celera | 11:97692803 | GGTCTCCAAGTAGCG[C/T]ACGATGCAGGTTTTG | 22658 |
rs263216679 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97698731 | GCTAAATCTCTCCTC[A/G]CTCCCGTTCTTTCCC | 22658 |
rs263363282 | snp | A/T | | | upstream-variant-2KB | Psmb3, Pcgf2 | Mm_Celera | 11:97702800 | CAGAACGTTCCTTTG[A/T]AGAGTGAACAGAGAC | 22658 |
rs263521157 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97697971 | CTCAGGGAGTTCCTT[C/T]CCCCCTCCCCTGCTC | 22658 |
rs263568472 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97696235 | TCCTCCAACAGCCCC[C/T]TCTGCCCCCGCCCCC | 22658 |
rs264198219 | snp | A/G | | | upstream-variant-2KB | Pcgf2, Psmb3 | Mm_Celera | 11:97701451 | GGCAAGTACTGTTTT[A/G]GGCACAGTAGGTAAG | 22658 |
rs264476010 | snp | A/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | Pcgf2 | Mm_Celera | 11:97699510 | CGAGGTAGCAAGGAG[A/G]CAAGCGCGAGTCGGC | 22658 |
rs265062932 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97690588 | CTGTAGCCGCCCCTA[C/T]TGCTGACCCCGAATC | 22658 |
rs265105933 | snp | C/T | | | upstream-variant-2KB, intron-variant | Pcgf2 | Mm_Celera | 11:97700009 | CCCACTTCCACCGAC[C/T]CTGCGATCCCTACCC | 22658 |
rs265227008 | snp | C/T | | | intron-variant | Pcgf2 | Mm_Celera | 11:97695545 | TCAACCCAGCACGTG[C/T]GCATGCACGCGCACA | 22658 |
rs265354167 | snp | A/C | | | intron-variant | Pcgf2 | Mm_Celera | 11:97692609 | GGGTCCTTCATCTCG[A/C]TAGCCGGGGATCAGC | 22658 |
rs265425505 | snp | A/G | | | intron-variant | Pcgf2 | Mm_Celera | 11:97694179 | GAAGAATAAATTGTC[A/G]CCACTCCACCAATGA | 22658 |
rs265712087 | snp | A/C | | | intron-variant | Pcgf2 | Mm_Celera | 11:97696768 | TCTTAACCAGCCCCC[A/C]CTCCATGTGATCTTT | 22658 |
rs266150842 | in-del | -/A | | | upstream-variant-2KB, utr-variant-5-prime | Pcgf2 | Mm_Celera | 11:97699572 | CTCGGGGAGGGGGGG[-/A]ATGGGAGGGAGGGAG | 22658 |
rs386987161 | in-del | -/AAACGAAC | | | intron-variant | Pcgf2 | Mm_Celera | 11:97690790 | AACAAACAAACAAAC[-/AAACGAAC]GAACGAAATGGCCTA | 22658 |
rs387052172 | in-del | -/A | | | utr-variant-3-prime, downstream-variant-500B | Cisd3, Pcgf2 | Mm_Celera | 11:97688601 | TAAAGCTGTCAATAA[-/A]CACTGAGGCCTGCCC | 22658 |
rs387381809 | in-del | -/A | | | intron-variant | Pcgf2 | Mm_Celera | 11:97696870 | CAGAAAAAAAAAAAA[-/A]CGGGCGATGCTCGGA | 22658 |
rs387487783 | in-del | -/A | | | utr-variant-3-prime, downstream-variant-500B | Cisd3, Pcgf2 | Mm_Celera | 11:97688607 | GTCAATAAACACTGA[-/A]GGCCTGCCCTCTAAC | 22658 |
rs387736742 | in-del | -/CGG | | | intron-variant | Pcgf2 | Mm_Celera | 11:97699135 | GGTCGGGGGCGGAGG[-/CGG]GGGGGGCGAGACCCA | 22658 |
rs387782568 | in-del | -/ACCCCAACCC | | | utr-variant-3-prime | Pcgf2 | Mm_Celera | 11:97689208 | TGTCTGGGGCCACCC[-/ACCCCAACCC]TCTACTCTAGGCCCC | 22658 |
rs578621187 | snp | G/T | | | intron-variant | Pcgf2 | GRCm38.p3 | 11:97696670 | TTTGTTTGTTTGTTT[G/T]TTTGTTTGTTTGTTT | 22658 |
rs578789980 | snp | C/T | | | utr-variant-3-prime | Pcgf2 | GRCm38.p3 | 11:97689453 | AGGACACAGACTGCA[C/T]TTGTGAAAGGCACTG | 22658 |
rs578989177 | snp | G/T | | | intron-variant | Pcgf2 | GRCm38.p3 | 11:97696650 | TCAGGCCCATAGTTT[G/T]TTTGTTTGTTTGTTT | 22658 |
rs579350534 | snp | C/T | | | intron-variant | Pcgf2 | GRCm38.p3 | 11:97696032 | GGGGGTGGGTGGGGG[C/T]TGAGGTGCTGGTGGG | 22658 |
rs579605918 | snp | A/G | | | intron-variant | Pcgf2 | GRCm38.p3 | 11:97690791 | AACAAACAAACAAAC[A/G]AACGAAATGGCCTAG | 22658 |
rs579798097 | snp | C/T | | | upstream-variant-2KB, intron-variant | Pcgf2 | GRCm38.p3 | 11:97699853 | AGCTCAGCTGCTCCC[C/T]ACCGCCTTGCGCTGG | 22658 |
rs580086807 | snp | G/T | | | utr-variant-3-prime | Pcgf2 | GRCm38.p3 | 11:97689255 | CAGTCTTGCTAGATT[G/T]CGTTCTTGGGTTGGG | 22658 |
rs580227892 | snp | A/C | | | intron-variant | Pcgf2 | GRCm38.p3 | 11:97697840 | CCCACCACCACTCCG[A/C]TATAGGGTCCGGGGT | 22658 |
rs580369363 | snp | C/T | | | intron-variant | Pcgf2 | GRCm38.p3 | 11:97692454 | ATGAGTGGGCGACAG[C/T]TGGGAAGTGGGGGTG | 22658 |
rs580504441 | snp | A/G | | | intron-variant | Pcgf2 | GRCm38.p3 | 11:97697010 | CCGCATTACAGATGG[A/G]GAAACTTAGGGCACA | 22658 |
rs580882758 | snp | A/T | | | intron-variant | Pcgf2 | GRCm38.p3 | 11:97693921 | CTGTGAGCCAGCGAG[A/T]GAACTCGGCAGGTAA | 22658 |
rs581225722 | snp | A/G | | | intron-variant | Pcgf2 | GRCm38.p3 | 11:97693062 | CGGCCCAACACAGAA[A/G]GTGCACCACGTCCTA | 22658 |
rs581536040 | snp | A/G | | | intron-variant | Pcgf2 | GRCm38.p3 | 11:97696034 | GGGTGGGTGGGGGCT[A/G]AGGTGCTGGTGGGGA | 22658 |
rs581867945 | snp | C/T | | | intron-variant | Pcgf2 | GRCm38.p3 | 11:97696672 | TGTTTGTTTGTTTGT[C/T]TGTTTGTTTGTTTTG | 22658 |
rs582253182 | snp | C/T | | | utr-variant-3-prime | Pcgf2 | GRCm38.p3 | 11:97689723 | AGACACCCCCACCCA[C/T]ACACACACATACACA | 22658 |
rs582446927 | snp | G/T | | | intron-variant | Pcgf2 | GRCm38.p3 | 11:97696666 | TTTGTTTGTTTGTTT[G/T]TTTGTTTGTTTGTTT | 22658 |
rs582751173 | snp | C/T | | | intron-variant | Pcgf2 | GRCm38.p3 | 11:97697182 | AAATCTCTTATCTTT[C/T]CTTTCTTTCTTTTTT | 22658 |
rs582945689 | snp | A/C | | | intron-variant | Pcgf2 | GRCm38.p3 | 11:97691632 | TGCAGGCCCAGCTAT[A/C]CAACTCTGTGATGGC | 22658 |
rs582997385 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | Pcgf2 | GRCm38.p3 | 11:97701240 | TACCTTTTGTTTATT[A/G]GGGTGGGTATCCATT | 22658 |
rs583460396 | snp | C/T | | | intron-variant | Pcgf2 | GRCm38.p3 | 11:97693402 | CAAGCTGGGCACCCC[C/T]GAATTCAACTCACAG | 22658 |
rs583651014 | snp | A/C | | | intron-variant | Pcgf2 | GRCm38.p3 | 11:97699130 | TCCTCGGGTCGGGGG[A/C]GGAGGGGGGGGCGAG | 22658 |
rs584144311 | snp | C/T | | | intron-variant | Pcgf2 | GRCm38.p3 | 11:97695746 | TAAGGGAAGGAGATG[C/T]TATGGATGGAAAGGT | 22658 |
rs585362832 | snp | G/T | | | intron-variant | Pcgf2 | GRCm38.p3 | 11:97696678 | TTTGTTTGTTTGTTT[G/T]TTTGTTTTGTTTCTC | 22658 |
rs585691630 | snp | C/T | | | utr-variant-3-prime | Pcgf2 | GRCm38.p3 | 11:97689733 | ACCCATACACACACA[C/T]ACACACACACACACA | 22658 |
rs586046481 | snp | A/G | | | intron-variant | Pcgf2 | GRCm38.p3 | 11:97691821 | AGGTGCATTCATGGC[A/G]CTCTCAGCCCACAGC | 22658 |
rs586256223 | snp | A/C | | | intron-variant | Pcgf2 | GRCm38.p3 | 11:97697837 | CGCCCCACCACCACT[A/C]CGCTATAGGGTCCGG | 22658 |
rs586795285 | snp | C/T | | | intron-variant | Pcgf2 | GRCm38.p3 | 11:97693653 | CGGGCCCAAAGTCCA[C/T]TTTTTTCCCCCGCTT | 22658 |
rs586978615 | snp | A/G | | | intron-variant | Pcgf2 | GRCm38.p3 | 11:97699141 | GGGGCGGAGGGGGGG[A/G]CGAGACCCACCCTAG | 22658 |