SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3691354 | snp | A/G | 0.5 | 0 | intron-variant | Pcgf5 | Mm_Celera | 19:36390022 | ATCTCCTGGACTTGC[A/G]GAAGTAATGAGAGAA | 76073 |
rs3692587 | snp | C/T | 0.5 | 0 | intron-variant | Pcgf5 | Mm_Celera | 19:36390216 | TTGAGAGGTTCCACC[C/T]TGATTTCCCAGCAAA | 76073 |
rs3705022 | snp | A/T | 0.324417 | 0.238667 | upstream-variant-2KB, intron-variant | Pcgf5 | Mm_Celera | 19:36377749 | GCCCCGACTACCTAC[A/T]AAGGCTCTTCACATC | 76073 |
rs3710581 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Pcgf5 | Mm_Celera | 19:36397464 | GAAAGTTAAGGTTTT[C/G]AAATTGTTTTGGAGA | 76073 |
rs6210492 | snp | C/T | 0.5 | 0 | intron-variant | Pcgf5 | Mm_Celera | 19:36385649 | CATTCCTTTAAGCtt[C/T]ctagtatgtatttgt | 76073 |
rs6210559 | snp | C/T | 0.5 | 0 | intron-variant | Pcgf5 | Mm_Celera | 19:36385694 | ctaaagcttatgtca[C/T]ttgtttcgttaagtg | 76073 |
rs6211623 | snp | G/T | 0.5 | 0 | intron-variant | Pcgf5 | Mm_Celera | 19:36385889 | TCATTCCCTCACTAG[G/T]ACATAGTGAGTACTT | 76073 |
rs6238606 | snp | C/T | 0.5 | 0 | intron-variant | Pcgf5 | Mm_Celera | 19:36399223 | CCACTATTGTTGTGC[C/T]TCCATAGCAAGGAGC | 76073 |
rs6239108 | snp | G/T | 0.5 | 0 | intron-variant | Pcgf5 | Mm_Celera | 19:36399287 | AGAATGTTTGTCTGT[G/T]GTATGTAGTCAGTGG | 76073 |
rs13483608 | snp | C/T | 0.499314 | 0.0185058 | intron-variant | Pcgf5 | Mm_Celera | 19:36412978 | TTGTATGAGTATACA[C/T]ACTTTCTGTGCTTTC | 76073 |
rs30314740 | snp | A/T | 0.5 | 0 | intron-variant | Pcgf5 | Mm_Celera | 19:36398564 | CCCGCCAGCCAATGG[A/T]GGCAGATCTAGGTCC | 76073 |
rs30316416 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Pcgf5 | Mm_Celera | 19:36409153 | TCTTCGATGTCTTAA[A/G]TTATATTTATTTATA | 76073 |
rs30316993 | snp | C/T | 0.375 | 0.216506 | downstream-variant-500B, utr-variant-3-prime | Pcgf5 | GRCm38.p3 | 19:36456695 | AAACAAAACAAACAA[C/T]GTACAGTAGATAAAT | 76073 |
rs30320437 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Pcgf5 | Mm_Celera | 19:36410691 | ATTTGCAAAACTTTT[A/T]AAATAACCTAACAAG | 76073 |
rs30320548 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pcgf5 | GRCm38.p3 | 19:36442012 | ATGTCCTAAAAATGT[C/T]CCCTTAACTATTTTG | 76073 |
rs30321244 | snp | A/G | 0.375 | 0.216506 | intron-variant | Pcgf5 | Mm_Celera | 19:36406807 | GAGCACCAGGAATGC[A/G]TTGATCTATCTTGCC | 76073 |
rs30355673 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pcgf5 | Mm_Celera | 19:36449820 | CACCATGTGGTTGCT[A/G]GGAATTGAACGCTGG | 76073 |
rs30372617 | snp | G/T | 0.49827 | 0.0293608 | intron-variant | Pcgf5 | GRCm38.p3 | 19:36429516 | AGGGGAGAAGTCTTA[G/T]TTGATATTGGGCAAG | 76073 |
rs30378143 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Pcgf5 | GRCm38.p3 | 19:36453115 | CATGACGTGTGGAGA[C/T]GGGACTTAGTGTGTG | 76073 |
rs30404468 | snp | C/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Pcgf5 | GRCm38.p3 | 19:36408900 | AATGAATGGTGTCTC[C/G]GAAGTCTCAAAGTCC | 76073 |
rs30406242 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Pcgf5 | GRCm38.p3 | 19:36450202 | CAACAAGTAGGAGAG[A/G]GATAGATGGTACCTC | 76073 |
rs30413988 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pcgf5 | GRCm38.p3 | 19:36412320 | CCTTTAAAACTGTTG[C/T]GCTCTGTTTTGGTCT | 76073 |
rs30418427 | snp | C/G | 0.375 | 0.216506 | intron-variant | Pcgf5 | GRCm38.p3 | 19:36439155 | ACATGAGCCTATGGG[C/G]GGGGGGTATCTCCTG | 76073 |
rs30419014 | snp | A/G | 0.375 | 0.216506 | intron-variant | Pcgf5 | GRCm38.p3 | 19:36415862 | GGCATCCCATTTAGG[A/G]ATGAGTGATCAGAAG | 76073 |
rs30448282 | snp | A/C | 0.487535 | 0.077957 | intron-variant | Pcgf5 | GRCm38.p3 | 19:36427109 | GGTAAGCACAGGGTT[A/C]GCTGTGAAGACCCTT | 76073 |
rs30449783 | snp | A/T | 0.492188 | 0.0620098 | intron-variant | Pcgf5 | Mm_Celera | 19:36447137 | ATACCAGCAGGAGAC[A/T]GGATGTCTACAAATT | 76073 |
rs30451036 | snp | A/G | 0.5 | 0 | intron-variant | Pcgf5 | Mm_Celera | 19:36399413 | GGAACATAAACCCAG[A/G]AACAACTGTATCATG | 76073 |
rs30453268 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Pcgf5 | GRCm38.p3 | 19:36447056 | CTGAAGAGATGGCTT[A/G]TTCTTCTCTAATCCT | 76073 |
rs30456783 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Pcgf5 | Mm_Celera | 19:36448545 | TGCCAGTGGGCATAG[A/G]CATTTGCTGAGATAG | 76073 |
rs30498890 | snp | A/T | 0.444444 | 0.157135 | utr-variant-3-prime | Pcgf5 | Mm_Celera | 19:36459834 | GCTTGATGTGTTTTA[A/T]TAAAACACAAACATG | 76073 |
rs30513635 | snp | C/T | 0.375 | 0.216506 | intron-variant | Pcgf5 | Mm_Celera | 19:36443317 | GGGATTAAAGGCGTG[C/T]GCCACCACACCCGGC | 76073 |
rs30542055 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pcgf5 | Mm_Celera | 19:36403587 | TACACATGCACCACA[C/T]AGGTGAAGACACCTT | 76073 |
rs30550429 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Pcgf5 | Mm_Celera | 19:36430436 | TAGTAATCTCTTTTT[C/T]ATTTTAAGGATATTT | 76073 |
rs30560278 | snp | A/T | 0.5 | 0 | intron-variant | Pcgf5 | Mm_Celera | 19:36398988 | TATGGCTATATCCAT[A/T]TTTTAATTTCATCTT | 76073 |
rs30570363 | snp | C/G/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Pcgf5 | GRCm38.p3 | 19:36409092 | CTTCATGTCCAGTAC[C/G/T]GCCTCGTGGGTCCAG | 76073 |
rs30605590 | snp | A/G | 0.375 | 0.216506 | intron-variant | Pcgf5 | Mm_Celera | 19:36416351 | AGGTCTGAGGATTCT[A/G]TAGCACATAGGATGA | 76073 |
rs30608002 | snp | A/C | 0.375 | 0.216506 | intron-variant | Pcgf5 | Mm_Celera | 19:36404736 | AGACATAGAGAGAAA[A/C]AGAGAGAGAGAGAGA | 76073 |
rs30648718 | snp | A/G | 0.49827 | 0.0293608 | utr-variant-3-prime | Pcgf5 | GRCm38.p3 | 19:36459680 | TTGTTTCCAGCATGG[A/G]ACTCCTCTGGGGAGC | 76073 |
rs30658571 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Pcgf5 | Mm_Celera | 19:36409148 | ACTGTTCTTCGATGT[C/T]TTAAGTTATATTTAT | 76073 |
rs30659837 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Pcgf5 | Mm_Celera | 19:36430366 | TTAGAGAGCATAATA[A/G]CCATCTCCCTGTAAA | 76073 |
rs30661509 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Pcgf5 | Mm_Celera | 19:36448898 | TACCACAGAAGAGGG[C/T]CCATTTTCTGACTTC | 76073 |
rs30661543 | snp | A/G | 0.375 | 0.216506 | utr-variant-3-prime | Pcgf5 | GRCm38.p3 | 19:36456738 | ACTAGTGGTGTGGGG[A/G]TGCTGTTATTTTAAA | 76073 |
rs30673378 | snp | A/G | 0.5 | 0 | intron-variant | Pcgf5 | Mm_Celera | 19:36399399 | TGGTTAGTTGGCCTG[A/G]AACATAAACCCAGGA | 76073 |
rs30694827 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Pcgf5 | Mm_Celera | 19:36394272 | GGTCCAGTGTCTGAG[C/G]GATCTTGGGGGTCCG | 76073 |
rs30700043 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pcgf5 | Mm_Celera | 19:36398369 | AAAACTGGCAGTATC[A/G]AAGTGGTCTGATAAC | 76073 |
rs30709354 | snp | A/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Pcgf5 | GRCm38.p3 | 19:36408272 | GCAGAAGTCATCCCA[A/T]CCTTGAGTCGGAGTT | 76073 |
rs30709851 | snp | C/G | 0.375 | 0.216506 | intron-variant | Pcgf5 | GRCm38.p3 | 19:36417358 | CAGATTACTGTATAT[C/G]TATATTTTACCTCCC | 76073 |
rs30711719 | snp | A/T | 0.432133 | 0.171253 | intron-variant | Pcgf5 | Mm_Celera | 19:36421400 | TATTGATGTCTGATA[A/T]ATAGGGACCAGAATG | 76073 |
rs30712349 | snp | A/T | 0.375 | 0.216506 | intron-variant | Pcgf5 | Mm_Celera | 19:36412487 | TTGTTTTTTCAAGAC[A/T]GGGTTTCTCTGTGTA | 76073 |
rs30748722 | snp | A/G | 0.5 | 0 | intron-variant | Pcgf5 | GRCm38.p3 | 19:36388636 | GGAGAAATATAGACC[A/G]TGGAACTTGTGGTCT | 76073 |
rs30760444 | snp | C/T | 0.5 | 0 | intron-variant | Pcgf5 | Mm_Celera | 19:36398579 | TGGCAGATCTAGGTC[C/T]GCAGCTGCAGCACCT | 76073 |
rs30768556 | snp | C/T | 0.375 | 0.216506 | intron-variant | Pcgf5 | GRCm38.p3 | 19:36399206 | TTAATTAAATAAATG[C/T]TCCACTATTGTTGTG | 76073 |
rs30769519 | snp | A/G | 0.375 | 0.216506 | intron-variant | Pcgf5 | Mm_Celera | 19:36404404 | TTAAAAGACAATATT[A/G]GACATTTTTCAATTG | 76073 |
rs30801943 | snp | C/T | 0.375 | 0.216506 | intron-variant | Pcgf5 | GRCm38.p3 | 19:36419970 | AAATCTTATGCCCCA[C/T]ACTCTTGCTATTCAA | 76073 |
rs30859683 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Pcgf5 | GRCm38.p3 | 19:36432840 | AAAGAGCACATACCA[A/G]GAATTTTCTAAAGGA | 76073 |
rs30865156 | snp | A/G | 0.375 | 0.216506 | intron-variant | Pcgf5 | Mm_Celera | 19:36412500 | ACAGGGTTTCTCTGT[A/G]TAGCCCTGGCTGTCC | 76073 |
rs30893337 | snp | C/T | 0.375 | 0.216506 | intron-variant | Pcgf5 | Mm_Celera | 19:36443407 | ACAGCTCTAGCTGCT[C/T]TTCCAGGTGACCGGG | 76073 |
rs30913423 | snp | A/C | 0.375 | 0.216506 | utr-variant-3-prime | Pcgf5 | GRCm38.p3 | 19:36457726 | GCAGGAAACAGCAAT[A/C]AGAATGCAGTTTTAT | 76073 |
rs30917354 | snp | A/G | 0.375 | 0.216506 | intron-variant | Pcgf5 | GRCm38.p3 | 19:36412743 | TTCCCCAATCACACT[A/G]TTGTCGGCATGCCCG | 76073 |
rs30932601 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Pcgf5 | Mm_Celera | 19:36428248 | AGGAGCTGGCGTGTG[A/G]GCACGTGTAATGTAA | 76073 |
rs30947530 | snp | C/T | 0.375 | 0.216506 | intron-variant | Pcgf5 | GRCm38.p3 | 19:36411529 | GTCAGATGCCCTGCC[C/T]GGAGGGTATCTGTCT | 76073 |
rs30948225 | snp | G/T | 0.432133 | 0.171253 | intron-variant | Pcgf5 | GRCm38.p3 | 19:36432559 | GCATCTCTTTGATTA[G/T]ATACCTTGGATTGGA | 76073 |
rs30957494 | snp | C/T | 0.5 | 0 | intron-variant | Pcgf5 | Mm_Celera | 19:36404044 | GAGTTGAGTCATAGT[C/T]TGCTGAGTATGAAGA | 76073 |
rs30959923 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pcgf5 | Mm_Celera | 19:36427648 | GTCTTCAGTAAAATA[A/G]GAAGTGAGGAGTGAG | 76073 |
rs30964645 | snp | A/G | 0.498615 | 0.0262793 | downstream-variant-500B, utr-variant-3-prime | Pcgf5 | GRCm38.p3 | 19:36456388 | AAATTCAAAATGTTG[A/G]CAGCTGATCATATCG | 76073 |
rs30982992 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Pcgf5 | GRCm38.p3 | 19:36409020 | TGATTGCTAGACCTA[C/T]CATACTGCTACAAGT | 76073 |
rs30988914 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Pcgf5 | Mm_Celera | 19:36444957 | ATTCAAATTTTCTCT[A/G]CATTAATATATTTTA | 76073 |
rs30995651 | snp | C/T | 0.375 | 0.216506 | intron-variant | Pcgf5 | Mm_Celera | 19:36443294 | CCTGCCTCTGCCTCC[C/T]GAGTGCTGGGATTAA | 76073 |
rs30998151 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pcgf5 | Mm_Celera | 19:36390545 | TGAATAAATCTAAAT[A/G]GGAAATAACTGACTG | 76073 |
rs31009948 | snp | A/G | 0.375 | 0.216506 | intron-variant | Pcgf5 | Mm_Celera | 19:36406688 | CTTTTGTCTTGGCTC[A/G]ACCCAAATCAGCTGT | 76073 |
rs31032347 | snp | A/G | 0.493827 | 0.0552116 | utr-variant-3-prime | Pcgf5 | GRCm38.p3 | 19:36459717 | GGACATGTCTGCTAG[A/G]TCTGGGTCATGATAA | 76073 |
rs31077104 | snp | C/G | 0.455 | 0.143091 | intron-variant | Pcgf5 | GRCm38.p3 | 19:36452659 | AGCAGTATGTAGCCT[C/G]CTCACATGGGCTCTT | 76073 |
rs31099321 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | Pcgf5 | GRCm38.p3 | 19:36459940 | CATTTGAAAGTGCTT[C/T]TCTTCCTGGACTATG | 76073 |
rs31103874 | snp | C/T | 0.5 | 0 | intron-variant | Pcgf5 | Mm_Celera | 19:36388049 | TGGGCATCAAGAGTG[C/T]GTGGAATGGAATAGA | 76073 |
rs31113009 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Pcgf5 | GRCm38.p3 | 19:36421789 | ATTGGTCCCTTGACT[A/G]CAGTGATACAGTTAT | 76073 |
rs31121361 | snp | A/G | 0.32 | 0.24 | intron-variant | Pcgf5 | Mm_Celera | 19:36413146 | GCAGTGGTTATAGGG[A/G]AAGAATATTTGGATT | 76073 |
rs31141195 | snp | C/G | 0.444444 | 0.157135 | utr-variant-3-prime | Pcgf5 | Mm_Celera | 19:36459192 | GCCCACAGGACAGCA[C/G]TCTGCTGGGTTTGCA | 76073 |
rs31148910 | snp | C/G | 0.444444 | 0.157135 | utr-variant-3-prime | Pcgf5 | GRCm38.p3 | 19:36459842 | TGTTTTATTAAAACA[C/G]AAACATGAAATTAAA | 76073 |
rs31187951 | snp | C/T | 0.32 | 0.24 | intron-variant | Pcgf5 | GRCm38.p3 | 19:36431776 | TCTTGCCCGTAATTT[C/T]AGCTCTACAGAGGCT | 76073 |
rs31188005 | snp | A/C | 0.375 | 0.216506 | intron-variant | Pcgf5 | GRCm38.p3 | 19:36435438 | TTTGGCCAAACATCC[A/C]TCAGAGATATTTGCA | 76073 |
rs31197994 | snp | A/G | 0.5 | 0 | intron-variant | Pcgf5 | GRCm38.p3 | 19:36404575 | TTCTTATGACCCCAA[A/G]AGCTGTACCTCCTTC | 76073 |
rs31207870 | snp | G/T | 0.497778 | 0.0332592 | utr-variant-3-prime | Pcgf5 | Mm_Celera | 19:36459208 | TCTGCTGGGTTTGCA[G/T]ATAGTAGAAGTACTG | 76073 |
rs31257729 | snp | A/T | 0.32 | 0.24 | utr-variant-3-prime | Pcgf5 | Mm_Celera | 19:36459067 | TTGAAATTGAGATTT[A/T]AAATTTTAAAAAGCC | 76073 |
rs31277040 | snp | A/T | 0.5 | 0 | utr-variant-3-prime | Pcgf5 | Mm_Celera | 19:36457695 | TCACATGTAATGACT[A/T]TTTTCCGAGGAGTAC | 76073 |
rs31281484 | snp | A/T | 0.497778 | 0.0332592 | intron-variant | Pcgf5 | GRCm38.p3 | 19:36447884 | CAAGGGCACTGCATA[A/T]CCGTGTCCCTCCCTC | 76073 |
rs31288947 | snp | C/G | 0.429688 | 0.173817 | intron-variant | Pcgf5 | GRCm38.p3 | 19:36428186 | ATCGTAACACAGGGA[C/G]CAAGCCTCTGGGAGC | 76073 |
rs36242100 | snp | A/C | 0.459184 | 0.136902 | intron-variant | Pcgf5 | Mm_Celera | 19:36419234 | TCAGGGACAAAGGAG[A/C]TTCATCCCAAAAGCT | 76073 |
rs36246102 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pcgf5 | Mm_Celera | 19:36432524 | TTTAGAACTTTGTGT[A/G]CCTTCGATGCTTCAG | 76073 |
rs36252474 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Pcgf5 | Mm_Celera | 19:36367679 | GTGGCTACGATCTCA[C/G]GATGTAACTGCCTTC | 76073 |
rs36253407 | snp | A/C | 0.124444 | 0.216185 | utr-variant-3-prime | Pcgf5 | Mm_Celera | 19:36459761 | CAAATGCACTAAAGT[A/C]TTCGAAGCACTTCAA | 76073 |
rs36261789 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Pcgf5 | Mm_Celera | 19:36429829 | ATTTAAGTTACCAGA[C/T]ACTATAAACCAGTGT | 76073 |
rs36264518 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Pcgf5 | Mm_Celera | 19:36367899 | TACCAAGGTCATTTT[A/G]ACTCAAGTGTGATTC | 76073 |
rs36267029 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pcgf5 | Mm_Celera | 19:36428756 | TCCTCAACATCAAAA[A/G]CTATGAAAAATATTG | 76073 |
rs36270302 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Pcgf5 | Mm_Celera | 19:36448669 | TTGGTACAATTCACT[G/T]TGTGTGGCTAGCAGG | 76073 |
rs36271706 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pcgf5 | Mm_Celera | 19:36444404 | TAATGAGCCATAGAC[A/G]AAGTTTCTGTGGCCT | 76073 |
rs36273230 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pcgf5 | Mm_Celera | 19:36435765 | ATTAGTGTTACACCA[C/T]GCTGTCAGATTGTTG | 76073 |
rs36275981 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pcgf5 | Mm_Celera | 19:36454458 | TAACCAACCAAGGTC[C/T]AAGCTGGTTCCTGAA | 76073 |
rs36277011 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Pcgf5 | Mm_Celera | 19:36421028 | AGAAAAAGAAAACGT[C/T]CAGATTGAAACTCCA | 76073 |
rs36281210 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Pcgf5 | Mm_Celera | 19:36370672 | TCCCCTCGAAAGGCA[A/G]CAGCAGCTCAAATCA | 76073 |
rs36284258 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Pcgf5 | Mm_Celera | 19:36377856 | GAACAGATGCTGCTG[C/T]GCTGTGACGAGGCAC | 76073 |