SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8164416 | snp | A/T | 0.299985 | 0.244952 | intron-variant, utr-variant-3-prime | Phf14 | Rn_Celera | 4:38375917 | AGGCATAGAGAAAAT[A/T]TTGAGTCAGATATAT | 500030 |
rs8168201 | snp | A/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38388288 | TCCTTAATAACTCAG[A/G]TTAATATCCACCATA | 500030 |
rs63778722 | snp | C/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38408373 | CTTGGCTGTGGCACT[C/T]CTTTTCTCTTCAGAC | 500030 |
rs63793909 | snp | C/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38349308 | TGGCACTGTGTTACA[C/T]AGGACATTGCCATCT | 500030 |
rs63935867 | snp | A/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38349942 | GCCAGCTTTTCCATA[A/G]GAGCGACTGACCTTA | 500030 |
rs63958712 | snp | A/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38349858 | TGACAGCTCCTAGGG[A/G]TCCATGTTAGTTGAC | 500030 |
rs64199198 | snp | G/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38349681 | AGCAAGGCAGCTCTG[G/T]CAGGGAACAGATACC | 500030 |
rs64213497 | snp | C/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38350199 | AGGGTCAAAAGTGTG[C/T]GTGGTTATTGTCCTT | 500030 |
rs64721333 | snp | C/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38348888 | AATTTGGGGTACATA[C/G]ACATTTTCTAAACAG | 500030 |
rs65256763 | snp | C/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38349807 | CTGGGGGCCTTGTTC[C/T]AGCCCGTGTATGCCG | 500030 |
rs65745544 | snp | C/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38408180 | CATAAGGCCCAGTCC[C/T]GTGTGTCATATCACT | 500030 |
rs66235122 | snp | A/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38350076 | CTGGTGTCAGAGATT[A/G]GTGCTTGCCCATGGA | 500030 |
rs104898021 | snp | C/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38394775 | CACAGAGAGTCCCCA[C/G]GGAGCTGTGCTTCTG | 500030 |
rs104901035 | snp | A/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38321922 | TGGTTTTTAGGTTCT[A/G]GACTGGGCTTCATGA | 500030 |
rs104904735 | snp | C/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38341585 | AAACACAATGTGACA[C/T]CCTTTCCTACTGTGT | 500030 |
rs104906821 | snp | C/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38348622 | ATGTTATCTCCTTTC[C/T]TGGTTTTCCCATTTG | 500030 |
rs104913785 | snp | A/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38258673 | ATGGTATTAAGCCAA[A/G]TCAAGATTCCAGATC | 500030 |
rs104937786 | snp | C/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38407368 | CTTAAAGTAATACCT[C/G]TGCTTCCGTCCTTAG | 500030 |
rs104938418 | snp | A/C | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38333986 | CTGTCCGGGATAACA[A/C]AATATCATTCTCATA | 500030 |
rs104940029 | snp | A/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38321076 | GCACCGTTTGTTGAA[A/G]ATGCTTTTGCTTCCC | 500030 |
rs104940735 | snp | G/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38355733 | GTTAAACTCCTTGCA[G/T]ACTATGGATTGTATC | 500030 |
rs104963640 | snp | C/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38264115 | TTTAGTTGTAGGAGT[C/G]AATGAACACCCTAAA | 500030 |
rs104963820 | snp | A/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38338460 | TTTATTTTTTTTAAT[A/G]ACAGATACAGTAAAA | 500030 |
rs104967298 | snp | A/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38262204 | AATTGTATGGAATCA[A/G]TAATACCTTATGCTA | 500030 |
rs104972186 | snp | G/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38305058 | ACTAAAGCAGTAGTT[G/T]GTGACTAGGCATGAG | 500030 |
rs104983373 | snp | C/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38310528 | GTGAGATATGGGAAA[C/G]CAAATTACTGTCTTT | 500030 |
rs104986360 | snp | A/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38328519 | TCAGTGAACTAGAAA[A/T]TTGGCAAATTTTTAC | 500030 |
rs105008987 | snp | C/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38269942 | CAGAGCTAGTGAGAA[C/G]TAGAGACAGGAGGAT | 500030 |
rs105010971 | snp | A/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38355002 | TCTGGGAATCTCCTG[A/G]GTTCTGGGTTAGTTG | 500030 |
rs105019252 | snp | C/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38368993 | CATGTATTAAGACTT[C/T]TCTTCCACAGAACAG | 500030 |
rs105025796 | snp | A/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38311192 | GTTTTATGTTTATAA[A/G]GCAAAGCTGAACTAA | 500030 |
rs105027719 | snp | A/C | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38278400 | TCTGCAGTATGAAGC[A/C]GAAACACAGACAGAG | 500030 |
rs105051245 | snp | C/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38347329 | AGCAGTAACCTTTCT[C/G]TGGATGTGTCTTTCC | 500030 |
rs105055002 | snp | A/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38338836 | TCATTCCTTTCCAAA[A/G]TGAATGTGTTAAATG | 500030 |
rs105059802 | snp | C/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38369267 | TCAAGCCCATGATTA[C/G]GCATACTACCTAATC | 500030 |
rs105062739 | snp | A/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38349790 | TATCTGTTACATATG[A/T]ACTGGGGGCCTTGTT | 500030 |
rs105069396 | snp | A/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38396132 | CCCACTGTGTCTGAG[A/T]TTTTTTTTTTAATTT | 500030 |
rs105103597 | snp | C/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38369065 | CCCACTCACTGTGTT[C/T]CTGTCATGTGTTTGG | 500030 |
rs105109951 | snp | C/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38347267 | CTATCAGTGCCTGCA[C/G]AGTTCTGTAAAAGGA | 500030 |
rs105114130 | snp | G/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38409833 | TTAACCCTTGATGGG[G/T]ACTAAGTCTTAATAA | 500030 |
rs105118014 | snp | C/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38387613 | GCCCCAGGAGGGTGG[C/G]TTCCTCTGCTGTTGT | 500030 |
rs105128370 | snp | G/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38358799 | TTCTTTGTATTAACT[G/T]TGTATTAACTCTTTG | 500030 |
rs105131683 | snp | A/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38364317 | AGGTTAATTTTCTGG[A/G]AACAATAAAGGCAGG | 500030 |
rs105133195 | snp | A/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38294499 | AATTAGTGGGTAAGT[A/G]GAAATTAAGGTTATT | 500030 |
rs105153299 | snp | C/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38392081 | AGCTTAGAGATTCAT[C/G]GTAACCACAGGCTTA | 500030 |
rs105162849 | snp | C/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38410216 | TACAAAAGTAAAATG[C/T]CATTATTAATGAGAA | 500030 |
rs105181720 | snp | A/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38288240 | GTTTTCAACCTTCCA[A/T]ATACTACCACCCTTA | 500030 |
rs105195643 | snp | C/G | 0.403751 | 0.197131 | intron-variant | Phf14 | Rn_Celera | 4:38250230 | GAAAGCTTTATAAAG[C/G]TTAAATACTAAGCTG | 500030 |
rs105215724 | snp | C/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38348091 | AACTGGTTGTTCCCA[C/T]TTCTCCTAACCTTAG | 500030 |
rs105221057 | snp | A/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38319821 | TGTGCCGCCCCTTCC[A/G]GGAGCTTCAGTGCAC | 500030 |
rs105228245 | snp | A/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38350683 | CAATACAAAAGCCTA[A/G]AATTAGGGGAAGAGT | 500030 |
rs105234111 | snp | C/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38361322 | TTTTGTAGTCTCAAA[C/T]TGAAGAAACCAGATT | 500030 |
rs105240106 | snp | A/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38349451 | AACCCCCAACCAAAA[A/G]ATTATTTTTGTTGCT | 500030 |
rs105240672 | snp | A/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38364631 | ACTTTGGATGATAGG[A/T]GAAAATACATTTGAT | 500030 |
rs105263275 | snp | C/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38362827 | TTTCTCAGAGTCACT[C/G]TATGATCCACTGAAT | 500030 |
rs105264185 | snp | A/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38410524 | AAATACTTCTGCATT[A/G]TCTTTGAGGCAGACT | 500030 |
rs105270256 | snp | A/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38275504 | CAGCACCATTTGCTG[A/G]AAATGCTATCTTTTT | 500030 |
rs105294161 | snp | C/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38286582 | GTCCACAAATAAAAT[C/T]TAGACTTAGATGTAA | 500030 |
rs105315176 | snp | C/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38282859 | TTCCAGGACTTGTAA[C/T]TTTGTGTTCTGACTT | 500030 |
rs105316910 | snp | A/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38396690 | GAGGATAGTGTTTTA[A/G]GAGGGTTAATTCTTA | 500030 |
rs105320764 | snp | A/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38341616 | GAGAGACATACCAAG[A/G]AAGATGCTAGAAAAT | 500030 |
rs105327937 | snp | A/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38289137 | ATATGAACAAAAAGT[A/G]CTCAAAGGAATAAAA | 500030 |
rs105330774 | snp | A/C | 0 | 0 | intron-variant, utr-variant-3-prime | Phf14 | Rn_Celera | 4:38371118 | CCCCTTTCAATATTC[A/C]GAAACACTTGGTGTA | 500030 |
rs105339694 | snp | C/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38359012 | GTCCCATAAGTTTGG[C/G]TACTGCGTGTTTTCA | 500030 |
rs105340152 | snp | C/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38329038 | ATTCTGTATAGCTTT[C/G]GACTTAATTTCATAG | 500030 |
rs105349211 | snp | G/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38379831 | TCTAAACTTATTTTA[G/T]TTAAGTAGAAAAGAT | 500030 |
rs105351946 | snp | A/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38277827 | AAAAATACCCAATTT[A/T]ATAAAGATGGAAAAA | 500030 |
rs105355187 | snp | C/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38412211 | CATCCTCACTTATGC[C/T]ACTTTCTTTTGTCCT | 500030 |
rs105362781 | snp | C/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38331421 | TGGTGGTTCTATATA[C/T]ATACATATACATGCA | 500030 |
rs105365910 | snp | C/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38335985 | ATTAATGGATCTTAT[C/T]GCTCCATTTTATATT | 500030 |
rs105371147 | snp | A/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38362963 | GGGAAAACGTAAAGT[A/T]TTGAAAGGATAGTGA | 500030 |
rs105372797 | snp | G/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38359931 | TCATCGAGTTTCTTA[G/T]TTTCATAATGACACT | 500030 |
rs105383388 | snp | A/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38418701 | GCATCTTGACAAATC[A/T]GGTGCCACCTAACAA | 500030 |
rs105388202 | snp | A/T | 0.5 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38270833 | AACCACACCTCAGAC[A/T]CTGAAAGTCTGTATA | 500030 |
rs105407802 | snp | C/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38415763 | GAACACAGTATAGCA[C/T]ATGCCCTTGATATAT | 500030 |
rs105408948 | snp | C/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38334859 | TCCCCAAATGCCTTG[C/T]CTGTATGTTCAGTCA | 500030 |
rs105433328 | snp | A/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38359060 | AAAGTCCTTTGTTTT[A/G]TTATTTATTTCTTCC | 500030 |
rs105446385 | snp | C/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38313758 | TCTGGCAGACCCTCT[C/T]AGGAGATAGCTATAT | 500030 |
rs105483136 | snp | C/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38348219 | GATTGCAAGTTTAAG[C/T]CTTTTGCACTTCATT | 500030 |
rs105485414 | snp | A/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38406441 | AGGTCATAAAATTCA[A/G]CAAAATACTTAACAA | 500030 |
rs105504432 | snp | C/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38272850 | CATGGCCCTAGCATC[C/T]CCCTATGCTGGGGCA | 500030 |
rs105516379 | snp | A/G | 0 | 0 | intron-variant, utr-variant-3-prime | Phf14 | Rn_Celera | 4:38373056 | TGCGTACGCATGCAC[A/G]CATGCATGCACGCAC | 500030 |
rs105540764 | snp | C/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38247191 | AGGTACAAGGACAAT[C/T]CGCATTCAATGCCAG | 500030 |
rs105549195 | snp | G/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38286112 | ATAAGCACATGTGGT[G/T]GTGTCTGTGGGGGTN | 500030 |
rs105549324 | snp | C/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38387712 | GGGAGCCTGGGATTG[C/T]GGGATTATGTGGTCT | 500030 |
rs105555461 | snp | C/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38410125 | TTTTCAAATAATGCA[C/G]AGCTTCTTACTGTGT | 500030 |
rs105570923 | snp | A/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38348008 | GGGACCCACCATCTG[A/G]AATAAGAGGCTGCCT | 500030 |
rs105574320 | snp | A/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38357794 | CATATGCGAGAATCA[A/G]TTCTCAGCCTCTGGC | 500030 |
rs105577131 | snp | G/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38326007 | CACTTCCACAGTAAA[G/T]CTGTCTTCTCAGACA | 500030 |
rs105582302 | snp | C/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38270273 | TGAGGTGGAACCTTG[C/T]TATTTTATCCAAACT | 500030 |
rs105588389 | snp | C/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38345202 | TGGTTTTATCTAAGT[C/T]AAGTGGCAATAGTAT | 500030 |
rs105598172 | snp | C/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38278005 | CAAACTTTTACTATA[C/G]CTTCAGACCTGAGCC | 500030 |
rs105601287 | snp | C/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38295117 | TGTTCTCTCACTAGC[C/T]GACCTACTCCTGCCT | 500030 |
rs105620662 | snp | A/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38359191 | GATCTGATAGAATGC[A/T]TTGGATTACTTTTCT | 500030 |
rs105623655 | snp | C/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38394552 | TATAGTCCATGTATG[C/T]TAGGTCAGATAATTT | 500030 |
rs105626389 | snp | C/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38286123 | TGGTGGTGTCTGTGG[C/G]GGTNTGAGCACACGA | 500030 |
rs105627112 | snp | C/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38294343 | ATTTTTTAATATCAG[C/T]TCTAAAATGTTATAT | 500030 |
rs105648407 | snp | A/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38357744 | AGATAAGTTGAAGAG[A/G]TTAACTGTCTACCAG | 500030 |
rs105649210 | snp | A/G | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38328392 | AAAAGTCGTAACTAT[A/G]GGTCAGCCTTTATGG | 500030 |
rs105657751 | snp | A/T | 0 | 0 | intron-variant | Phf14 | Rn_Celera | 4:38276203 | CATATCATCTGCAAA[A/T]AGTGATATTTTGACT | 500030 |