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 |