SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3023445 | snp | C/T | | | utr-variant-3-prime | Ccnf | GRCm38.p3 | 17:24223673 | TACCCTTCTGTGTCC[C/T]GTTGTCTCCGGGAGC | 12449 |
rs3023446 | snp | C/T | 0.3848 | 0.210544 | utr-variant-3-prime | Ccnf | GRCm38.p3 | 17:24223671 | CCCTTCTGTGTCCTG[C/T]TGTCTCCGGGAGCAT | 12449 |
rs3678863 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Ccnf | Mm_Celera | 17:24244179 | ACGACTACAGCAGGG[A/G]CATGAGTCATTCTGT | 12449 |
rs3679391 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Ccnf | Mm_Celera | 17:24244214 | AATATATCAGAACTG[A/G]AATTACTCAGTTTTC | 12449 |
rs3679485 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Ccnf | Mm_Celera | 17:24244271 | GGCTTCCATGAGAAG[A/G]TGACTCACATCTGAG | 12449 |
rs3691006 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | GRCm38.p3 | 17:24240987 | ACAGTGCTGACTGAT[C/T]ACGGCAGAAATGAGG | 12449 |
rs3692227 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24241187 | CAGATCACAGAGCCC[A/G]AGACAAACCTCAAGG | 12449 |
rs3692229 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | GRCm38.p3 | 17:24241189 | GATCACAGAGCCCGA[A/G]ACAAACCTCAAGGGA | 12449 |
rs3692817 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24241267 | CACCTCCATCACTTA[G/T]CCTCCAAGCTGTCCT | 12449 |
rs4139614 | snp | C/T | 0.5 | 0 | intron-variant | Ccnf | Mm_Celera | 17:24244398 | TGAGCTCTCCAGTTT[C/T]CGGTCTCTTTCAGGG | 12449 |
rs4139618 | snp | C/G | 0.5 | 0 | intron-variant | Ccnf | Mm_Celera | 17:24244399 | GAGCTCTCCAGTTTC[C/G]GGTCTCTTTCAGGGG | 12449 |
rs6243977 | snp | A/T | 0.5 | 0 | intron-variant | Ccnf | Mm_Celera | 17:24238271 | GACTCAAAAACAGCA[A/T]AAAGATTAAATAGAA | 12449 |
rs13459672 | snp | C/T | | | utr-variant-3-prime | Ccnf | GRCm38.p3 | 17:24223354 | TTGTATCCATGTGAC[C/T]GTATCTCTGCACTGA | 12449 |
rs13459673 | snp | C/T | 0.375 | 0.216506 | missense | Ccnf | GRCm38.p3 | 17:24223914 | ACAGTGACAAGGACA[C/T]GCACCTGGCTTCCTG | 12449 |
rs13459674 | snp | A/G | 0.375 | 0.216506 | missense | Ccnf | GRCm38.p3 | 17:24226575 | GCTGACTTGTGCAGT[A/G]CAATAGGAGTAAAAC | 12449 |
rs13459675 | snp | C/T | | | synonymous-codon | Ccnf | GRCm38.p3 | 17:24223985 | GTGTCGTCCCCCAAA[C/T]TCCCCAGAGAGCGGT | 12449 |
rs13459676 | snp | C/T | | | synonymous-codon | Ccnf | GRCm38.p3 | 17:24224995 | AATCAGGAGGAGACA[C/T]TGCTAGGCAGCCTTC | 12449 |
rs13459677 | snp | C/T | | | synonymous-codon | Ccnf | GRCm38.p3 | 17:24244533 | CAGTGTGTGGGCATC[C/T]GCCAGCTTCCAGGAG | 12449 |
rs13459678 | snp | C/G | 0.444444 | 0.157135 | synonymous-codon | Ccnf | Mm_Celera | 17:24224081 | CATGGGGGGCTCTCC[C/G]CAATCTACCTCAGTG | 12449 |
rs13459679 | snp | A/G | | | synonymous-codon | Ccnf | GRCm38.p3 | 17:24225068 | TTGCAGGAAGCGAGA[A/G]AACAGCCTTCAGGAG | 12449 |
rs29497480 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | GRCm38.p3 | 17:24235580 | CATAGGTCCTGGGAA[C/T]TGAACTCAGGGTTTC | 12449 |
rs29499473 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ccnf | Mm_Celera | 17:24246321 | CAGACAACTTGGCAA[C/T]TGTGAAAGATTTCTG | 12449 |
rs29500388 | snp | A/G | 0.375 | 0.216506 | utr-variant-3-prime | Ccnf | GRCm38.p3 | 17:24223772 | TGGTCACTGAGCTCA[A/G]TGTCCTGACAGCTTG | 12449 |
rs29500670 | snp | C/T | 0.32 | 0.24 | intron-variant | Ccnf | GRCm38.p3 | 17:24236826 | AAACAATGGAAGATT[C/T]GTGACATCAAGTTTG | 12449 |
rs29502478 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ccnf | Mm_Celera | 17:24248612 | TGATGGCAGTCCCAA[C/T]ACTCCAGAGGTAAAA | 12449 |
rs29540104 | snp | C/G | 0 | 0 | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | GRCm38.p3 | 17:24236396 | AAAAGTTGTATTTTA[C/G]CTTCAGAAATCGGAG | 12449 |
rs33048445 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ccnf | Mm_Celera | 17:24227049 | ATGACTGCTTCATTC[A/G]GAGATGTCCAGAGTG | 12449 |
rs33081401 | snp | C/T | 0.32 | 0.24 | intron-variant, downstream-variant-500B | Ccnf, Mir5134 | Mm_Celera | 17:24234210 | CTTCCTCGCAAAGGA[C/T]ACTGGGATTGAAATT | 12449 |
rs33088667 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | Mm_Celera | 17:24236553 | ATTCAGGGCTAGTCT[A/G]AGCTACAACAGGACT | 12449 |
rs33106953 | snp | A/T | 0.444444 | 0.157135 | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24252569 | TCAGTTGATCAGTTG[A/T]CTTTTTTTTTTTTTT | 12449 |
rs33125495 | snp | G/T | 0.375 | 0.216506 | intron-variant | Ccnf | GRCm38.p3 | 17:24238966 | AAACCTCTGACAGTC[G/T]TAGACATGAACACAA | 12449 |
rs33136780 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24252962 | TTGTGACCTAGAAGT[A/G]TAAGACAAATAAATT | 12449 |
rs33152038 | snp | A/G | 0.375 | 0.216506 | downstream-variant-500B, upstream-variant-2KB | Ccnf, 1600002H07Rik | Mm_Celera | 17:24222834 | CAGGCTTCAGCAGAC[A/G]CCCCAGGTGTTGAGG | 12449 |
rs33158489 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ccnf | GRCm38.p3 | 17:24226938 | TATCAACGGTCAGAC[A/G]GACAAAGGTCCATTG | 12449 |
rs33169247 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | Mm_Celera | 17:24235753 | TGCGCACAGAACCTC[C/T]GGAACCCACTCATCT | 12449 |
rs33174569 | snp | G/T | 0.5 | 0 | intron-variant | Ccnf | Mm_Celera | 17:24239523 | TAGGGGCCAGAGATA[G/T]CTCAGAGGTTTAGGA | 12449 |
rs33180378 | snp | G/T | 0.375 | 0.216506 | intron-variant | Ccnf | Mm_Celera | 17:24248714 | AAAAACCACTCTTGG[G/T]GCTGGAGAGATAGCA | 12449 |
rs33221762 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ccnf | GRCm38.p3 | 17:24248874 | TACTGCATGCACATG[A/G]TGTATACAAGTTATG | 12449 |
rs33273241 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ccnf | Mm_Celera | 17:24226992 | TTGACCCAGAAATGG[A/G]ATACTCAATTGAGAA | 12449 |
rs33278010 | snp | C/T | 0.32 | 0.24 | synonymous-codon | Ccnf | GRCm38.p3 | 17:24231884 | CACAGCCTCTCTAAT[C/T]GTCAGAATCTCTTTG | 12449 |
rs33282036 | snp | A/C | 0.375 | 0.216506 | intron-variant | Ccnf | GRCm38.p3 | 17:24227310 | AACTCACTCTGTAGA[A/C]CTGGCTGGCTTTGAA | 12449 |
rs33282352 | snp | C/G | 0.375 | 0.216506 | intron-variant | Ccnf | Mm_Celera | 17:24239935 | GACATCTGTCAACAA[C/G]AGAAAGTTATCCTCA | 12449 |
rs33286786 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ccnf | Mm_Celera | 17:24239704 | GACAAGCATATGTAT[A/G]TAAATAAGTAAAAAC | 12449 |
rs33309135 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Ccnf | GRCm38.p3 | 17:24226953 | AGACAAAGGTCCATT[C/G]AAACACCAACACACA | 12449 |
rs33316055 | snp | A/G | 0.32 | 0.24 | synonymous-codon | Ccnf | Mm_Celera | 17:24231809 | CCCTTCCAGGGCGGA[A/G]ATGATCTCCCCCATC | 12449 |
rs33335541 | snp | A/G | 0.32 | 0.24 | intron-variant | Ccnf | GRCm38.p3 | 17:24236610 | CAAGTACAAGCACTG[A/G]CATTTGGATCCAGAA | 12449 |
rs33348082 | snp | A/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | GRCm38.p3 | 17:24236014 | CCAAAATTTTACTTG[A/T]AATTTCAGATGAAAG | 12449 |
rs33352118 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ccnf | Mm_Celera | 17:24246711 | TTCATAGGAGAAAAA[C/T]GGATAAATAAAGGGA | 12449 |
rs33359023 | snp | A/T | 0.375 | 0.216506 | intron-variant | Ccnf | Mm_Celera | 17:24246955 | AAATTGCTAAATAAA[A/T]TTTGTCTGGTTTTGT | 12449 |
rs33379980 | snp | A/T | 0.375 | 0.216506 | intron-variant | Ccnf | Mm_Celera | 17:24248936 | AAAAAAAAAAAAGAT[A/T]AAACCACGCAATTCT | 12449 |
rs33386536 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ccnf | GRCm38.p3 | 17:24246582 | ATTCTGACACACAGC[A/G]TTTCCCTATTTCCCA | 12449 |
rs33414417 | snp | A/C | 0.32 | 0.24 | intron-variant | Ccnf | Mm_Celera | 17:24244094 | GGGGGTCTCAGACAG[A/C]GGGCCTGGTCACTGG | 12449 |
rs33430360 | snp | A/T | 0.375 | 0.216506 | intron-variant | Ccnf | GRCm38.p3 | 17:24239599 | CACATCAGGTGGCTC[A/T]CAAGTGCCTGTAACT | 12449 |
rs33464932 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ccnf | Mm_Celera | 17:24248525 | ATTCTGGACTAAAAA[A/G]GCACTTCTGGACCAT | 12449 |
rs33500352 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ccnf | Mm_Celera | 17:24248582 | AGGTAAGGAAGAGCC[A/G]GGTAAGATGGTCACT | 12449 |
rs33516921 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ccnf | Mm_Celera | 17:24239800 | GTTTAAAGCCTAGGC[A/G]GTCCTGCCCCAAGGT | 12449 |
rs33526137 | snp | A/G | 0.32 | 0.24 | intron-variant, downstream-variant-500B | Ccnf, Mir5134 | GRCm38.p3 | 17:24234125 | CAGGCTCTGGGTCCC[A/G]AGACTGTGTGGGGGA | 12449 |
rs33585643 | snp | A/T | 0.375 | 0.216506 | intron-variant | Ccnf | GRCm38.p3 | 17:24248885 | CATGGTGTATACAAG[A/T]TATGCAGGCAAAACA | 12449 |
rs33594489 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Ccnf | GRCm38.p3 | 17:24230305 | GACGACAGATTCAGA[C/G]TCGGACTCACCACTT | 12449 |
rs33635863 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ccnf | Mm_Celera | 17:24248548 | TGGACCATGCTGAGC[C/T]AAGTAAGGCACTGTC | 12449 |
rs33648783 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | Mm_Celera | 17:24236394 | CCAAAAGTTGTATTT[C/T]ACCTTCAGAAATCGG | 12449 |
rs33658626 | snp | C/T | 0.375 | 0.216506 | missense | Ccnf | Mm_Celera | 17:24226749 | CGGCCGTCAGAGAGA[C/T]TTGTCTGTAGTCTTT | 12449 |
rs33664820 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ccnf | Mm_Celera | 17:24246624 | CAGCGTGAGTATAAA[C/T]TGCTATCTCCTTAGG | 12449 |
rs33666307 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ccnf | Mm_Celera | 17:24239005 | GACAAGAGATCAGCC[A/C]GGACCATCTGTTGAT | 12449 |
rs33680096 | snp | A/C | 0.444444 | 0.157135 | downstream-variant-500B | Ccnf | Mm_Celera | 17:24223118 | CAGATGACCCAGGCC[A/C]CGTTGACTTGGAGCT | 12449 |
rs33685094 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ccnf | Mm_Celera | 17:24230292 | TCCAGTGTTGAGAGA[C/T]GACAGATTCAGACTC | 12449 |
rs33705056 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ccnf | Mm_Celera | 17:24227002 | AATGGGATACTCAAT[C/T]GAGAAGCCAGATTCA | 12449 |
rs33886857 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ccnf | Mm_Celera | 17:24227399 | TCATAAAACTTAAAC[A/G]ATCAGAGTGGGTAGA | 12449 |
rs45656682 | snp | C/G | | | intron-variant | Ccnf | Mm_Celera | 17:24250099 | TTGACCAAGGGACTT[C/G]CATAGCATAGACTGG | 12449 |
rs45682217 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24242879 | AGACCAGGGCAGGAC[A/G]GAAGCTCTTTCCTCA | 12449 |
rs45709832 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24231106 | GAACTCAGAAATTCA[C/T]CTGCCCTTGACTCCC | 12449 |
rs45791827 | snp | A/T | | | intron-variant | Ccnf | Mm_Celera | 17:24244005 | GAAAATCCTATGCTG[A/T]GTTAGTTTCTCAGCT | 12449 |
rs45830230 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24242061 | ACTTTAAACGGCCCA[C/T]GGAACGTGCTTCAGG | 12449 |
rs45835889 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | GRCm38.p3 | 17:24234804 | ATCTCAATCCCTGCT[C/T]ATAGGCAGTGGGTAC | 12449 |
rs45856256 | snp | C/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24236966 | CATCAAATTACTAAA[C/G]AGCTCACCCGCTCAC | 12449 |
rs45861457 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24239391 | TTGTGACAGCAGCAG[C/T]ACTGAGAATTAAGAG | 12449 |
rs45867292 | snp | A/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24238937 | TGAGCCATCTTACTA[A/T]TAACATTTTCTGTAA | 12449 |
rs45874666 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24232948 | AGTACTAACAATCAG[A/G]AACACTCTGTTCCAG | 12449 |
rs45884175 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24250259 | GCAAAATCACCCCTT[C/T]CTAGCACCGTGGACC | 12449 |
rs45910340 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24245438 | CGCTCCAAAAACTGT[A/G]CAACAGTCCAAAGAT | 12449 |
rs45945353 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24244702 | TCAGCATGGTAAAGA[A/G]CTCAACTTCCATGTA | 12449 |
rs45989186 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24241692 | CGGCCCCACTCAGGC[C/T]ATATTTATTTCATAT | 12449 |
rs46051542 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24233110 | GCCTATCTGAAGAAG[A/G]CCCGGGATGCGGTAA | 12449 |
rs46075176 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24226930 | CATGTGTCTATCAAC[A/G]GTCAGACGGACAAAG | 12449 |
rs46104481 | snp | C/G | | | intron-variant | Ccnf | Mm_Celera | 17:24230691 | AAATTAAATATAAAT[C/G]TAAAGTCAAGATAAA | 12449 |
rs46141393 | snp | G/T | | | intron-variant | Ccnf | Mm_Celera | 17:24243157 | TCCTTAGAACCTATA[G/T]CCAAGTGTCAAGGGC | 12449 |
rs46159122 | snp | A/T | | | intron-variant | Ccnf | Mm_Celera | 17:24237977 | GGACTCTCTCTGAGG[A/T]TCGTGCTCACGTGTC | 12449 |
rs46279886 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24244622 | TGTGAGAATCACTGA[A/G]GGACTTCCCAAATCC | 12449 |
rs46339049 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24246986 | TTAAAAACAAAATAA[A/G]ACAAACAACTATGAA | 12449 |
rs46377222 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24245202 | ACGGTGCTGACACTT[C/T]CAGGGATATGATAAC | 12449 |
rs46396963 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24236935 | ATCAATCAATGTGGA[A/G]CGGAAATACTTTCTT | 12449 |
rs46400275 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24238516 | GTTTGTCAAAGGGGT[A/G]AAGATCCACAGGCTG | 12449 |
rs46474250 | snp | A/C | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | GRCm38.p3 | 17:24241160 | CCTAGCCTACACCTG[A/C]AAAGGGACCCACAGA | 12449 |
rs46519417 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24232629 | ACTGCATCTGAGTAC[A/G]AAGAATGCAAACATA | 12449 |
rs46545142 | snp | C/G | | | intron-variant | Ccnf | Mm_Celera | 17:24226237 | TCTCCCTGAAAGTAA[C/G]AGAGATAAAACAAGA | 12449 |
rs46556986 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24232388 | CATGGCACAGTCTAC[C/T]CTAGCTGTTCTCTCC | 12449 |
rs46577676 | snp | C/T | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24252629 | TTTCAGTTTCTATTA[C/T]TTATTGGAGGCGGGT | 12449 |
rs46587970 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24237633 | AAATGGCGCATCGAT[A/G]GCCTTGGAGTCAGAT | 12449 |
rs46698558 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24245217 | TCAGGGATATGATAA[A/C]CTTGACGATACGTTT | 12449 |
rs46712483 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24250024 | TACTGCATTCTAAGT[A/G]TTAGTCACTATGGCC | 12449 |
rs46785400 | snp | A/C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24244829 | AACCTGGCACGGTAA[A/C/T]TCACACCTTAGTACT | 12449 |
rs46795015 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24244732 | ATGAAAATAAGACTG[C/T]TTTGTACAGAGATAA | 12449 |
rs46865969 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24225126 | ACAGATGGCAGCACC[C/T]GGAGAGCCAACGTAA | 12449 |
rs46963471 | snp | A/C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24233372 | TGACCTTCATCCCAG[A/C/T]GGGCCGGATGTTCTG | 12449 |
rs47078756 | snp | A/G | | | synonymous-codon | Ccnf | GRCm38.p3 | 17:24231806 | CTTCCCTTCCAGGGC[A/G]GAAATGATCTCCCCC | 12449 |
rs47141269 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24242507 | CCTTCAGGAAGCTTG[A/G]ATTCTGACCCTCAAA | 12449 |
rs47232936 | snp | C/G | | | intron-variant | Ccnf | Mm_Celera | 17:24250796 | AAATTTACAGCAAAG[C/G]CCAAATGTATACCCA | 12449 |
rs47266793 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24251012 | AAGAGTCCGGACAGG[A/G]CCTGAGATCGCTCTA | 12449 |
rs47295720 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24231276 | CCCAAGATACCAGGT[C/T]ACCCTCCACAGCCCC | 12449 |
rs47348972 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24232811 | ACACACAGCCCTCCC[A/G]GTGTAGGAGGGCTAC | 12449 |
rs47360329 | snp | C/G | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24252257 | GCCCTGGCTGACCTG[C/G]AACTCACTCTGTAGA | 12449 |
rs47428997 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24233429 | TGATCCAAGAGTCAC[A/G]TGGGAAGAAATCTTA | 12449 |
rs47433618 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24226445 | GTGAGGGAGCGAGCC[A/G]TGGCGTGGCTGCAGA | 12449 |
rs47462374 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | GRCm38.p3 | 17:24235160 | GGGCAAGAGATCCTT[A/G]TCTAAAGCTGAGGGG | 12449 |
rs47474661 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24245462 | CAAAGATGACCTCAA[A/G]TTCCTATACACCAAA | 12449 |
rs47488742 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24230519 | AAAATACCCTTAATG[A/G]TGGGCCAGTGATATG | 12449 |
rs47569482 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24241593 | TTCCAGCCACCAATA[C/T]ATTCACTAAGACACC | 12449 |
rs47570485 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24250073 | TTGAACATGTGACTA[C/T]CAGCATATGGTTGAC | 12449 |
rs47600946 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24237668 | GTGGACTGAGATGTG[C/T]CAACACTTAGGAGAC | 12449 |
rs47625283 | snp | C/G | | | intron-variant, missense | Ccnf | Mm_Celera | 17:24251228 | GGGTCACAGGGGCCC[C/G]AGTCCATGCTCCTCC | 12449 |
rs47646167 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24243108 | GCTCTGCTCAGTCAT[C/T]CTTTGCCGATCCAAA | 12449 |
rs47718493 | snp | G/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24226896 | TCTCACATAGGAGCA[G/T]TCAGAGGCTGAGATC | 12449 |
rs47738566 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24247201 | TGGGAGGCAGAGGCA[A/G]GCGGATTTCTGAGTT | 12449 |
rs47740574 | snp | G/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24231630 | TAATGACACACCGCA[G/T]CCATGGCTTCCTGGT | 12449 |
rs47744958 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | GRCm38.p3 | 17:24241077 | TCTAAGCAGCACGGA[C/T]GGTGGCAGTGGTGGC | 12449 |
rs47768797 | snp | C/G | | | intron-variant | Ccnf | Mm_Celera | 17:24243191 | CAAAGGGCTGACCAG[C/G]AGCAAGATCTAAGCT | 12449 |
rs47792236 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24239068 | ATCTACCATCCATGC[A/G]GTGGGGCAACAAGAA | 12449 |
rs47828429 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24227885 | AGAGAGGCAGCCTCA[C/T]GGTATTAGCACAGTC | 12449 |
rs47988978 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24251171 | CTCGCAGTCGGGGAT[A/C]CGTGCCTACCCCGTG | 12449 |
rs48047366 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24224482 | CAAGCTGGAAAGGTT[C/T]CCCTTGATAACTCAC | 12449 |
rs48048490 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24227662 | GAAGACACCGAGCCT[A/G]TGACAGTCACCTTGC | 12449 |
rs48096855 | snp | C/G | | | intron-variant | Ccnf | Mm_Celera | 17:24224521 | AGAAAGTGACAAACT[C/G]GTCACCTAACTCACT | 12449 |
rs48116850 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | GRCm38.p3 | 17:24235144 | AAGCCCAATGCTTCT[C/T]GGGCAAGAGATCCTT | 12449 |
rs48175617 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24245157 | TCTAAAGGCATCTAT[A/G]CCTAACAACTCCAGC | 12449 |
rs48188145 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24226352 | CCTGGGTTGATCTGG[A/G]AGCTGCTGTACAAAC | 12449 |
rs48198163 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24245302 | AGATACGCCACATAA[C/T]AAGCTGGCATGGTGA | 12449 |
rs48279088 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | GRCm38.p3 | 17:24235248 | AGAAGGGGCAGGCTT[C/T]GCCTCAGCTCAGACT | 12449 |
rs48287518 | snp | C/T | | | missense | Ccnf | Mm_Celera | 17:24224161 | CTGAGGTCGTAATGT[C/T]CTTGGCCCGATCTCC | 12449 |
rs48311158 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24239212 | TGGCAAAGCAGGATT[A/G]GCTGAAAGCTCTAAA | 12449 |
rs48458638 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24242356 | AGAAACAGGCAAAGC[C/T]ATGATGTCTCTGGGG | 12449 |
rs48482651 | snp | G/T | | | synonymous-codon | Ccnf | Mm_Celera | 17:24226725 | ACTTATCCTCGAACC[G/T]CTGCTTCACGGCCGT | 12449 |
rs48506717 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24232782 | ACACACAGCCCTCCC[A/G]GTGTAGGAGGGCTAC | 12449 |
rs48540973 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24226264 | AAGACAGACAGGCTC[A/G]AGTAACAACAACAAC | 12449 |
rs48692405 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24244029 | CTCAGCTGTGACAAG[A/C]AAAGGCTCAAGCTCA | 12449 |
rs48761068 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24228345 | GCCCAGTACCTGTCT[A/G]CACCAGCCCTGTACC | 12449 |
rs48846227 | snp | A/C/G | | | upstream-variant-2KB | Ccnf | GRCm38.p3 | 17:24252198 | CTATACTGTTTTCCA[A/C/G]TTTGTTACTTTTTCT | 12449 |
rs48900021 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24225959 | GGAGCACACAGCGCA[C/T]TGAGGACTCCCAAGG | 12449 |
rs48907597 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24226077 | GGTCTGGGAGATAAG[A/G]ACAGACACAGGGCAG | 12449 |
rs49066398 | snp | A/G | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24252613 | TTTGTATCCTACTCA[A/G]TTTCAGTTTCTATTA | 12449 |
rs49088955 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24249987 | CCTTGAACTCCTGAT[C/T]CCCCTACCTCTACCT | 12449 |
rs49106212 | snp | A/T | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24252121 | AGAGCAAGACTTGGG[A/T]TTTGCTCCCCATTGC | 12449 |
rs49211579 | snp | C/G | | | intron-variant, downstream-variant-500B | Ccnf, Mir6965 | Mm_Celera | 17:24240504 | GTCTATCCCACACCA[C/G]ATGAGGTCACATGAA | 12449 |
rs49220436 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24239349 | GGCATGGTCTACAGA[A/G]CAATGTTCCAAAGTG | 12449 |
rs49238429 | snp | A/T | | | utr-variant-3-prime | Ccnf | Mm_Celera | 17:24223380 | TACAATGGGACACAG[A/T]CAAACCACTTTGGGA | 12449 |
rs49269146 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24232672 | CTGCTGGAGCACGGT[A/G]GAGGGCTACACACAG | 12449 |
rs49284198 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24231623 | GGGCAGCTAATGACA[C/T]ACCGCAGCCATGGCT | 12449 |
rs49413676 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24244620 | CATGTGAGAATCACT[A/G]AAGGACTTCCCAAAT | 12449 |
rs49477298 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24225347 | CACCCTACAGGGTAC[C/T]AGACACACCAGACAG | 12449 |
rs49498749 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24228258 | AAATGGGAGGAACCA[A/G]ACTGCAAGCCAAGCT | 12449 |
rs49611681 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24230195 | CCTTTCTGAAAACAG[A/G]GTCTTGGTACACAGT | 12449 |
rs49644256 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24227721 | AGGAAACTGGGTAGC[A/C]AAAGCATAATAATAC | 12449 |
rs49671438 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24232537 | TTAAGGTTTGTTTGG[C/T]TGTGCTGTGGTTCAA | 12449 |
rs49672756 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24238327 | AGCTCATTTAAAGCT[A/G]TAGCTCCAAATTCAT | 12449 |
rs49711834 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | GRCm38.p3 | 17:24236105 | TTGTGTTATCACTAA[C/T]GTTTGAAGCCTGGAA | 12449 |
rs49769216 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24225102 | AGGGAGAGTCCATAA[A/G]CCCTGGCCACAGATG | 12449 |
rs49787090 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24225651 | ACCTCCAGTAGGTAC[A/C]CATGTCTGTCTGAGA | 12449 |
rs49799314 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24229194 | CAAACACAGCCCACA[C/T]AGAGTCTGAAGCACA | 12449 |
rs49811767 | snp | C/T | | | missense | Ccnf | GRCm38.p3 | 17:24226712 | ATTTCCTCATAGCAC[C/T]TATCCTCGAACCTCT | 12449 |
rs49861854 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24232142 | CAGACAAGAATGTAC[A/G]AGTGTCGGGTCCCGA | 12449 |
rs49863336 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24244471 | CCAACACTCAGAACA[A/C]AGGCATACCTTTCAA | 12449 |
rs49886720 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24242907 | TCAGGTGTCTTTTAC[A/G]GAGCAGCTGGCCTTG | 12449 |
rs49893428 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24225132 | GGCAGCACCTGGAGA[A/G]CCAACGTAATGCTAT | 12449 |
rs49965905 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24250267 | ACCCCTTCCTAGCAC[C/T]GTGGACCCTTTAATA | 12449 |
rs49981897 | snp | C/T | | | utr-variant-3-prime | Ccnf | Mm_Celera | 17:24223741 | GTGGCTGCTGTCCAA[C/T]ACGTAGAGGCTGAGC | 12449 |
rs49988019 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | GRCm38.p3 | 17:24235042 | GACACAAGAAGGCCG[A/G]CAAAAGTCTCTCTCT | 12449 |
rs49999406 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24247159 | TTCTTGCGGGCAGTG[A/G]TGGCGCACGCCTTTA | 12449 |
rs50007508 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | GRCm38.p3 | 17:24235127 | CGTAAGGACACCCTA[A/G]TAAGCCCAATGCTTC | 12449 |
rs50021321 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24247480 | ACAAATAATAAATAA[C/T]CTTTGGGCTGGAGCG | 12449 |
rs50047604 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24242842 | AACTGGTATTCTATA[C/T]TCTAAATGCTATACA | 12449 |
rs50082756 | snp | G/T | | | intron-variant | Ccnf | Mm_Celera | 17:24240158 | AAGAAGCCTCCCCTT[G/T]GCTAACCAAATTTCA | 12449 |
rs50090169 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24231138 | AGTGCTGGGATTAAA[A/G]GTGTGCGCCACCACT | 12449 |
rs50122636 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24231621 | CAGGGCAGCTAATGA[C/T]ACACCGCAGCCATGG | 12449 |
rs50136151 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | Mm_Celera | 17:24235946 | AGCATTTACTAAACA[C/T]AGTTCATGTTCCAAG | 12449 |
rs50314681 | snp | G/T | | | intron-variant | Ccnf | Mm_Celera | 17:24238348 | CCAAATTCATAAACC[G/T]CCTGCCTCAGCCTCT | 12449 |
rs50333060 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24224589 | CAGGTGAAACTTGCC[C/T]AAGTCAGTGTTCCTG | 12449 |
rs50340615 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24239121 | TCTGCAAAGATGTCT[C/T]GGATTTGTTCTAAAG | 12449 |
rs50357377 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24242576 | GGGAAATGACCCTGC[A/G]AATGATTGGAAGGAA | 12449 |
rs50378496 | snp | C/T | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24252375 | TTGTTACTTTTTTAT[C/T]TTCCTCCTTTTGTAC | 12449 |
rs50381835 | snp | A/C | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24241350 | CACCACAGGGCAAGG[A/C]GTGGCTCTGTATTCA | 12449 |
rs50404424 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24231228 | GAGGGAGTGTTCATT[C/T]CCTCCCTTCCAACCT | 12449 |
rs50433411 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24231517 | GGGAGGAAAATGCCA[C/T]GTCTCATCCATCAGT | 12449 |
rs50513697 | snp | C/G | | | intron-variant | Ccnf | Mm_Celera | 17:24233296 | GGGAGCTTTGGCGGT[C/G]ACAGGAAAAAGAACC | 12449 |
rs50547030 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24230063 | GTTTTTGGCATGAAA[A/C]ATTGCAAGAGGACAT | 12449 |
rs50587322 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24226329 | CAGGCCTCGGCCAAG[C/T]CCAAGCCCCTGGGTT | 12449 |
rs50599384 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | GRCm38.p3 | 17:24235999 | GTTTCCCATCATAAA[C/T]CAAAATTTTACTTGA | 12449 |
rs50605170 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24233137 | GTAAGGTCAGATGTT[C/T]CCCCCTGAAATCCAC | 12449 |
rs50620820 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24250546 | TTGTTCCAATATTTA[C/T]TTCAGCAATTCATTC | 12449 |
rs50675138 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24227860 | GGGCTGAACGGAAAG[A/G]ACGTGCTATAGAGAG | 12449 |
rs50698946 | snp | C/T | | | synonymous-codon | Ccnf | GRCm38.p3 | 17:24231312 | AGGCCTCTCCTTACT[C/T]TGCCCATGCATGAGT | 12449 |
rs50722424 | snp | C/G/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | GRCm38.p3 | 17:24235433 | TAACAAGCTTAATAA[C/G/T]CCGACTTCTTTTTAA | 12449 |
rs50792284 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24245474 | CAAATTCCTATACAC[A/C]AAACACTTACTGGGC | 12449 |
rs50800925 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24225477 | CTGGGAGAGCCTGCT[A/G]CACTCACCAGGCCTT | 12449 |
rs50818783 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24251032 | AGATCGCTCTATATC[A/G]TGTGGATTGCCCACG | 12449 |
rs50898161 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24231103 | CTTGAACTCAGAAAT[C/T]CACCTGCCCTTGACT | 12449 |
rs50964989 | snp | C/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24232583 | CGCCAAGCTTCTAAA[C/G]AACCGCTTCAGCTCC | 12449 |
rs50999431 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24237339 | GCTTCCTTAGCAGCA[C/T]GGCTAAGAGCTCTAG | 12449 |
rs51016910 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | GRCm38.p3 | 17:24242386 | GGATGGGAAGAGAGC[A/G]CCAGTCTTTCTGTCC | 12449 |
rs51027556 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24224414 | AGCTGCTCAGGACTG[C/T]GGGGCCCAGGCTATT | 12449 |
rs51042067 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24239096 | GAACAAGCTTTCCCC[A/G]TTGTGGCAATCTGCA | 12449 |
rs51042833 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24233786 | AGAAGAGTAAGAAAA[C/T]GCAAACTACATTTTG | 12449 |
rs51046348 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | GRCm38.p3 | 17:24234766 | AAATCCGAGTCAGCC[C/T]GCAGCCACCAAAGCA | 12449 |
rs51046921 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | Mm_Celera | 17:24234970 | TGCCACTTAAAGTAA[A/G]AGCCACTCAGTGCCT | 12449 |
rs51048076 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24245067 | CTTGCGTATCCCAAC[A/G]GAAGTGAGCATGGCT | 12449 |
rs51055251 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24243102 | TCTGGGGCTCTGCTC[A/G]GTCATCCTTTGCCGA | 12449 |
rs51056316 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24225998 | GCAAGGGAGGAGGCT[A/G]GGTGTCACAGGATCC | 12449 |
rs51089591 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24241108 | TCTCACCGCTCACCC[A/G]CCTCCCTTGTCTTGC | 12449 |
rs51092319 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24237306 | CAGGCAGCCACACAG[C/T]ACACACGGCCAGCCT | 12449 |
rs51113033 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24227969 | GACCCAGCCATCAGC[A/C]GGTCGTACAGACGAA | 12449 |
rs51135219 | snp | G/T | | | intron-variant | Ccnf | Mm_Celera | 17:24250151 | TCTGTAGAACATGGA[G/T]GCCAGATCCATCCCA | 12449 |
rs51178215 | snp | C/T | | | synonymous-codon | Ccnf | GRCm38.p3 | 17:24237167 | GAGCTGGCAGACCGA[C/T]TCACTGCAGGCCTTC | 12449 |
rs51283646 | snp | G/T | | | intron-variant | Ccnf | Mm_Celera | 17:24226200 | GGAGAGATCTGAACA[G/T]GATCTACTGTGTTCA | 12449 |
rs51285529 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24233101 | GGTCACAGAGCCTAT[C/T]TGAAGAAGACCCGGG | 12449 |
rs51295742 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24245154 | CTTTCTAAAGGCATC[C/T]ATACCTAACAACTCC | 12449 |
rs51310321 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24225273 | AGAACTGGGCAAGGT[C/T]AGGCTTCAGAATAGG | 12449 |
rs51456805 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24233764 | CCAAGCTGGGGCCAT[C/T]AAGTTTAGAAGAGTA | 12449 |
rs51469782 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24226005 | AGGAGGCTGGGTGTC[A/G]CAGGATCCACAACTC | 12449 |
rs51539280 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24245249 | AAAAACCAAGGTACA[C/T]CAGGATCACCCTAAG | 12449 |
rs51593609 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24231268 | AAGACTTCCCCAAGA[C/T]ACCAGGTCACCCTCC | 12449 |
rs51625895 | snp | A/C | | | intron-variant, nc-transcript-variant | Ccnf, Mir5134 | GRCm38.p3 | 17:24234585 | AGCATCACAGCTGCC[A/C]TTTCTGCCAAGTCTG | 12449 |
rs51646658 | snp | C/G | | | intron-variant | Ccnf | Mm_Celera | 17:24226046 | GGAGCTATTCTAGGA[C/G]GTATAGCAAAGGGCT | 12449 |
rs51697191 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24225893 | CCACCATCACAGAAC[A/G]CTCATGGCTCATAAG | 12449 |
rs51700108 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | GRCm38.p3 | 17:24242709 | TAGGTACAAGAACGA[C/T]GTCTGGGTATGGTCA | 12449 |
rs51712998 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24241946 | TCTCTTCTTTACAGG[A/G]GCACTATAGCTAGAA | 12449 |
rs51733679 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24244983 | GTGGTGGTCTATACT[A/G]CAAGTTCACGTTAGC | 12449 |
rs51751255 | snp | G/T | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24252642 | TATTTATTGGAGGCG[G/T]GTTTTGTTGGTTTTG | 12449 |
rs51761948 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24243140 | TAGGAAAGGGGGTGA[C/T]TTCCTTAGAACCTAT | 12449 |
rs51781423 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | GRCm38.p3 | 17:24235198 | AACAGGAAGCAAGAG[A/G]GAAAAGGCGCAATGA | 12449 |
rs51781907 | snp | G/T | | | intron-variant | Ccnf | Mm_Celera | 17:24245264 | TCAGGATCACCCTAA[G/T]CTACAACACACTTTT | 12449 |
rs51832642 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24237934 | TGACTTTCGTCTACA[C/T]GTATCCAAGGACTCT | 12449 |
rs51881373 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24233997 | CTCAGTGACAGTTTA[C/T]CTCTGATGACTGAGG | 12449 |
rs51901365 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24244882 | CCAGTCAGGGCAGAG[A/G]GTAGTGTCTCTGTCC | 12449 |
rs51929862 | snp | C/T | | | utr-variant-3-prime | Ccnf | Mm_Celera | 17:24223333 | GGCAAAGAATGGCCT[C/T]GAAATTCAGTGCAGA | 12449 |
rs51931195 | snp | C/G | | | intron-variant | Ccnf | Mm_Celera | 17:24244810 | CTATGCTAAGAAAGA[C/G]ATGAACCTGGCACGG | 12449 |
rs51931741 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24237684 | CAACACTTAGGAGAC[A/G]CTGCCTGGCACCCAC | 12449 |
rs51949105 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24225109 | GTCCATAAACCCTGG[C/T]CACAGATGGCAGCAC | 12449 |
rs52001257 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24243980 | GGTCTGGGAAGGAAG[C/T]GCTCAGGAGGAAAAT | 12449 |
rs52017769 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24241286 | CCAAGCTGTCCTGTC[C/T]ACCTCCTTCCAAGGC | 12449 |
rs52113965 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24238284 | CAAAAAGATTAAATA[A/G]AACACATTAATGAGA | 12449 |
rs52349155 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24247833 | AATTATGGGTATACA[C/T]ACACCACAGCGTGTG | 12449 |
rs52514305 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24247843 | ATACACACACCACAG[C/T]GTGTGTGTGGAAGTC | 12449 |
rs52594737 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24224621 | CCAGAACACAGGGAA[A/G]AGGACCTCCTGCAGT | 12449 |
rs52596614 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24243895 | CACGTTATCCAAAAT[C/T]AGCTCAAGCATGGCA | 12449 |
rs52604304 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24227618 | AGATAAACATCAGGT[A/C]ACAATCAGTGGAAGT | 12449 |
rs52641283 | snp | A/T | | | intron-variant | Ccnf | Mm_Celera | 17:24238386 | AAAGATTAAGCTCCT[A/T]TATTTGGCAAATGTT | 12449 |
rs52643534 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24238270 | TGACTCAAAAACAGC[A/G]AAAAGATTAAATAGA | 12449 |
rs52644230 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24227435 | TTTAACATACATAAA[A/G]CCCTGAGGTCTATCC | 12449 |
rs52651291 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24246255 | TAAGATAGCCACAGT[A/G]TGTCGTCTGCAGCAC | 12449 |
rs52655997 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24224731 | CACGACAGGATCTAA[A/G]TGAGGTCCTTCAACC | 12449 |
rs107595519 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24237519 | AGGTGATTGTAAGTA[A/G]CCATGTGACTGACGG | 12449 |
rs107612625 | snp | A/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24248061 | CACAACCATCTGTAA[A/T]GGGATCTGATGCCCT | 12449 |
rs107625076 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24242466 | GGTGGGGCTCCACTT[C/T]TCTAAGACAGGCCCC | 12449 |
rs107627953 | snp | C/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24230454 | CCCACAATTCCTACA[C/G]TTCTGGTAGTTCCGT | 12449 |
rs107648470 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24233329 | TCATGGAGCTCAGAG[A/G]GGAGCAAATGTGAGC | 12449 |
rs107654383 | snp | A/T | | | intron-variant | Ccnf | Mm_Celera | 17:24245616 | CACAGAGAGACCCTG[A/T]TGAAAGAAAGAAAGA | 12449 |
rs107668005 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24237236 | GGCCAAAGCCAGCTA[C/T]GGGGAGAGATAAGGC | 12449 |
rs107679919 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24233120 | AGAAGACCCGGGATG[C/T]GGTAAGGTCAGATGT | 12449 |
rs107680848 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24232191 | TCACTGAATACCTAT[A/G]GCTCCTCCCAGCACT | 12449 |
rs107680975 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24228618 | GTCTCGTGGAAGAGC[A/G]TCCAGTGCTCTGACC | 12449 |
rs107708948 | snp | A/C | | | intron-variant | Ccnf | GRCm38.p3 | 17:24237545 | GACGGGAAATGCCCG[A/C]AGGTCCTCTTGGAGA | 12449 |
rs107720585 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24232183 | GACAAGTCTCACTGA[A/G]TACCTATAGCTCCTC | 12449 |
rs107725029 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24229901 | GTCAGATCTCGTTAC[A/G]GATGGTTGTGAGCCA | 12449 |
rs107736355 | snp | A/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24236918 | AAAAGTAAAAAAAAA[A/T]TATCAATCAATGTGG | 12449 |
rs107740803 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24228310 | GCCCAGTGTCCAAGA[C/T]ACTCCCTTTAGAGCC | 12449 |
rs107756882 | snp | C/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24240289 | ATCTATCCCACACCA[C/G]ATGAGGTCACATGAA | 12449 |
rs107771131 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24229445 | CTGAGTTCAAATCCC[A/G]GCAACCACATGGTGG | 12449 |
rs107782960 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24241631 | TTTCTTTTCTTTTTT[C/T]TTTTTTTTTTCTTTT | 12449 |
rs107785844 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24229430 | GCTCTTCCAAAGGTT[C/T]TGAGTTCAAATCCCG | 12449 |
rs107788759 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24233555 | GAGCAAGCCACTATG[C/T]GGCACCCCTCCATGG | 12449 |
rs107822818 | snp | C/G | | | intron-variant | Ccnf | Mm_Celera | 17:24229376 | AAAATGCCAACCCAG[C/G]GGGCTGGTGAGATGG | 12449 |
rs107838865 | snp | A/T | | | intron-variant | Ccnf | Mm_Celera | 17:24236713 | ACTCCAGCTGTTGTG[A/T]GAGGCTGGGTTGGGA | 12449 |
rs107841816 | snp | A/C | | | intron-variant | Ccnf | GRCm38.p3 | 17:24247299 | AGAAAAAAAAAAAAA[A/C]AAAAAACCCCAAAAC | 12449 |
rs107845797 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24229582 | AAAAAGAAAGCCAAC[C/T]CAGGGCTGACCAGAC | 12449 |
rs107846444 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | GRCm38.p3 | 17:24235844 | TACCAAACTCAAGTC[A/G]CCATTCTTGTGCATC | 12449 |
rs107855268 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24232235 | TACCCTGAACCTTTT[A/G]CAGTCCAGGGGCTGG | 12449 |
rs107856560 | snp | A/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24232848 | CCCTCCCGGTGTAGG[A/T]GGGCTACACACAGCC | 12449 |
rs107859338 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24228042 | GAGCAGCAGCTCAGA[A/C]GTACAAGCGAGGTGG | 12449 |
rs107891403 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24228797 | CCATCTCCTTCCCAC[C/T]TCCCACCCATTCAAC | 12449 |
rs107904058 | snp | A/C | | | intron-variant | Ccnf | GRCm38.p3 | 17:24243454 | ACTGAATTTTTTTTT[A/C]ATGAAATCAAATACT | 12449 |
rs107910110 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | GRCm38.p3 | 17:24235011 | TCCCTCATCCAGCAC[C/T]CCAGATGGATGCCCA | 12449 |
rs107916575 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24229469 | ATGGTGGCTCACAAA[C/T]ATCCGTAACAAAAAA | 12449 |
rs107918677 | snp | A/T | | | intron-variant | Ccnf | Mm_Celera | 17:24230688 | TAGAAATTAAATATA[A/T]ATGTAAAGTCAAGAT | 12449 |
rs107923682 | snp | A/C | | | intron-variant | Ccnf | GRCm38.p3 | 17:24237541 | GACTGACGGGAAATG[A/C]CCGAAGGTCCTCTTG | 12449 |
rs107943538 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24240081 | TTTGGGGGGGGGGGC[A/G]GGGAGTAATAGTAGC | 12449 |
rs107954853 | snp | A/T | | | intron-variant, downstream-variant-500B | Ccnf, Mir6965 | Mm_Celera | 17:24240702 | ATGAAACTGTGCCTG[A/T]GGTCTATCCCACACC | 12449 |
rs107961052 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24229066 | GTATCCGCTGTTGGG[C/T]ACAGGCTAAGGTTAA | 12449 |
rs107961883 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24239308 | ACCCCTCCACTCCCA[A/G]GCAGCCTGGCATCTG | 12449 |
rs107973099 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24237567 | TCTTGGAGAGCAGGC[A/G]GAGCTCTTAACCACA | 12449 |
rs107973844 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24229584 | AAAGAAAGCCAACTC[A/G]GGGCTGACCAGACAG | 12449 |
rs107975781 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24245394 | AGGGGGAGTAGCACC[C/T]AAGATTCTCAGTTTC | 12449 |
rs107994010 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | GRCm38.p3 | 17:24242453 | TGGAGCTCTGTGGGG[C/T]GGGGCTCCACTTCTC | 12449 |
rs108005054 | snp | A/T | | | intron-variant | Ccnf | Mm_Celera | 17:24243722 | ACTGTGAATACACTA[A/T]AAACCAAGCCCCACC | 12449 |
rs108005568 | snp | C/G | | | intron-variant | Ccnf | Mm_Celera | 17:24245403 | AGCACCTAAGATTCT[C/G]AGTTTCCAATGCAAA | 12449 |
rs108017957 | snp | A/C/G/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24240327 | CTGTGGTCTATCCCA[A/C/G/T]ACCAGATGAGGCCAC | 12449 |
rs108023563 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24225171 | GCCTCAATGCCCACA[C/T]GCCCCTGGCTCTCAC | 12449 |
rs108025739 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24243891 | CACACACGTTATCCA[A/G]AATTAGCTCAAGCAT | 12449 |
rs108025973 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24229572 | TTAAAAAAAAAAAAA[A/G]AAAGCCAACTCAGGG | 12449 |
rs108026898 | snp | C/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24231723 | GCCCGCCCCCCCCCC[C/G]CCCCCCGTGACCTCA | 12449 |
rs108027404 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24228580 | TTCGGAGCCTCCATG[C/T]GGATGCTAGGAACTG | 12449 |
rs108029721 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24228954 | TCAGGAACCATAATA[C/T]ACACAAAGACCCCTA | 12449 |
rs108031111 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24230844 | GGATCCAATGCCCTC[C/T]TCTGATGTGCCTGAA | 12449 |
rs108033753 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24237514 | GCTACAGGTGATTGT[A/G]AGTAGCCATGTGACT | 12449 |
rs108034530 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24237532 | TAGCCATGTGACTGA[C/T]GGGAAATGCCCGAAG | 12449 |
rs108038600 | snp | A/T | | | intron-variant | Ccnf | Mm_Celera | 17:24229652 | GAGGAGCGGAGTGCA[A/T]GTCCTAGAACCCACA | 12449 |
rs108053134 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24245533 | ACTTGGGAGGCAGGG[A/C]CAGGTAGAGCTCTGT | 12449 |
rs108061229 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24230588 | ACTTAGAACTGATTC[C/T]GGGAAGCCACATGGT | 12449 |
rs108096543 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | GRCm38.p3 | 17:24235435 | ACAAGCTTAATAATC[C/T]GACTTCTTTTTAAAA | 12449 |
rs108102489 | snp | A/G/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24244783 | CTGATGTTCTGAGGC[A/G/T]GAAGGAAAGACCTAT | 12449 |
rs108107785 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24242546 | GGCTCCTACATCCTC[C/T]ACCTTCCTCCTCGAG | 12449 |
rs108120032 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | GRCm38.p3 | 17:24241629 | TTTTTCTTTTCTTTT[C/T]TCTTTTTTTTTTCTT | 12449 |
rs108124288 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24228899 | TGTGTAACACACACA[C/T]AGACACACACACACA | 12449 |
rs108125330 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24229643 | ATTAAGCCTGAGGAG[C/T]GGAGTGCAAGTCCTA | 12449 |
rs108133898 | snp | C/G | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | GRCm38.p3 | 17:24235803 | ATTATAGGCACATGC[C/G]ACTCCCTCAGACCTC | 12449 |
rs108137842 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24229377 | AAATGCCAACCCAGG[A/G]GGCTGGTGAGATGGC | 12449 |
rs108147499 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24246259 | ATAGCCACAGTGTGT[C/T]GTCTGCAGCACAACT | 12449 |
rs108168718 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | GRCm38.p3 | 17:24234665 | CTCCGAGTCCCCCAC[A/G]GCAACTCCCAGGAGG | 12449 |
rs108171728 | snp | A/C/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24244789 | TTCTGAGGCAGAAGG[A/C/G]AAGACCTATGCTAAG | 12449 |
rs108173553 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24228583 | GGAGCCTCCATGCGG[A/G]TGCTAGGAACTGAGC | 12449 |
rs108176376 | snp | C/G | | | intron-variant | Ccnf | Mm_Celera | 17:24238657 | GTAAGCCATGAGCAA[C/G]CCCCCATCCACAGCC | 12449 |
rs108180720 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24229756 | TAATAATAACAACAA[C/T]AATAATAAAAAATAA | 12449 |
rs108188845 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24237466 | TCTGGTGACAAGGAG[A/G]GCAGAATAAAGTGTC | 12449 |
rs108194848 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24228490 | TTTGCCTGCAGGTAC[A/G]TCTGCACCACAAGTA | 12449 |
rs108196241 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | Mm_Celera | 17:24236595 | TAAGTATTTGCTGAA[C/T]AAGTACAAGCACTGG | 12449 |
rs108203809 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24228442 | TTCTTTCTTTACAAA[A/G]GTTTATTTATTTTTG | 12449 |
rs108205258 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24237326 | ACGGCCAGCCTGGGC[C/T]TCCTTAGCAGCATGG | 12449 |
rs108209109 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24238795 | ATTTTTTGGTCATGG[C/T]GTTTCATCACCGCAA | 12449 |
rs108228358 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24232337 | CCTCCGTCCAGCTCC[C/T]CTCTTCCTCTCTGCG | 12449 |
rs108236397 | snp | G/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24238563 | GACATTGTCAGTGAC[G/T]GATGGGGGAGGGCCC | 12449 |
rs108245288 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | Mm_Celera | 17:24235782 | CTCCACTTCCTCAGT[A/G]TCAGGATTATAGGCA | 12449 |
rs108251514 | snp | C/G | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24251987 | CCTTCATCCCCTCCC[C/G]GAAGCCAGCATGCTC | 12449 |
rs108275365 | snp | A/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24237619 | TTTTCTCTGTTATGA[A/T]ATGGCGCATCGATGG | 12449 |
rs108285514 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24225380 | ACAATGCAGGGCCTG[A/C]CTGCAGTCTGTCTTT | 12449 |
rs108289257 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24227776 | CAGTGGGGAGGCAGG[A/G]GGGCAGAGAAGATGC | 12449 |
rs108294334 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24237274 | AAGTCCTGGCCTGTC[C/T]GCTCAGAGGGGCTCA | 12449 |
rs108306293 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24237637 | GGCGCATCGATGGCC[C/T]TGGAGTCAGATGAGG | 12449 |
rs108313723 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24229125 | ATTAGAGAAAACTGG[C/T]TTTTCCTATTCTGGC | 12449 |
rs108319142 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24245412 | GATTCTCAGTTTCCA[A/G]TGCAAACCCACGCTC | 12449 |
rs108354953 | snp | A/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | GRCm38.p3 | 17:24235823 | CCTCAGACCTCCAGT[A/T]CTGGGTACCAAACTC | 12449 |
rs108367024 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24240085 | GGGGGGGGGGCGGGG[A/G]GTAATAGTAGCTCAC | 12449 |
rs108370687 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24236902 | ACATAGAAATGGGGG[A/G]AAAAGTAAAAAAAAA | 12449 |
rs108373689 | snp | A/C | | | intron-variant | Ccnf | GRCm38.p3 | 17:24237890 | GTGGACCATTTGATT[A/C]CCTCCCTGCTGAGTT | 12449 |
rs108378677 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24236699 | GTGACCAACTGTTAA[C/T]TCCAGCTGTTGTGTG | 12449 |
rs108394935 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24245619 | AGAGAGACCCTGTTG[A/C]AAGAAAGAAAGAAAG | 12449 |
rs108396498 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24228530 | ACGGAGGCCAGGAGA[C/T]GGCACGGGAACCTGT | 12449 |
rs108399853 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24230927 | TTTTTAAAAAAAGAC[C/T]CCATACACAGTATAC | 12449 |
rs108419215 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24230487 | CATTTACCCAGACTC[A/G]GGCTTTTAGTCCCTT | 12449 |
rs108427069 | snp | C/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24236747 | CCAGAGCAATACAGT[C/G]AGTTCACTGTTAGGC | 12449 |
rs108433570 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24245220 | GGGATATGATAACCT[C/T]GACGATACGTTTTAA | 12449 |
rs108435694 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24225730 | ATACAGAGCACAGTG[C/T]AAACTGTGGCTTTCT | 12449 |
rs108436887 | snp | A/G | | | intron-variant, downstream-variant-500B | Ccnf, Mir6965 | Mm_Celera | 17:24240720 | TCTATCCCACACCAG[A/G]TGAGGCCACATGAAA | 12449 |
rs108437987 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24240274 | GAAACCATGCCTGTG[A/G]TCTATCCCACACCAG | 12449 |
rs108439525 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24236765 | TTCACTGTTAGGCTA[A/G]CTCTGGTTTGCCAGA | 12449 |
rs108451562 | snp | C/G | | | intron-variant | Ccnf | Mm_Celera | 17:24243757 | ACTCCAGTTCAAGAG[C/G]ATCTGGCGCCCTCTA | 12449 |
rs108454954 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24233465 | TTGCTATGGGAGGGC[C/T]CAGCTCACTGTGGGT | 12449 |
rs108461936 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24229111 | CCCTGTGAGAGTCCA[C/T]TAGAGAAAACTGGTT | 12449 |
rs108465889 | snp | A/C | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | GRCm38.p3 | 17:24235326 | AGGAACAGGACAGGA[A/C]AGGTCTACTCCCCAC | 12449 |
rs108490261 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24230095 | TGGACTGAGTGACAG[C/T]AGCTAGGTGATAAAG | 12449 |
rs108493447 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24230071 | CATGAAAAATTGCAA[A/G]AGGACATGTGGACTG | 12449 |
rs108514772 | snp | G/T | | | intron-variant | Ccnf | Mm_Celera | 17:24230531 | ATGATGGGCCAGTGA[G/T]ATGGCTCCGTGGGCA | 12449 |
rs108518246 | snp | C/T | | | intron-variant, downstream-variant-500B | Ccnf, Mir6965 | Mm_Celera | 17:24240726 | CCACACCAGGTGAGG[C/T]CACATGAAACCGTGC | 12449 |
rs108526922 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24233316 | GAAAAAGAACCACTC[A/G]TGGAGCTCAGAGGGG | 12449 |
rs108537695 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24233620 | CCTGCTCAAGCTCCT[A/G]CCCTGACTTTCCTCA | 12449 |
rs108549429 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24242437 | CCACACTGCAAAGCT[C/T]TGGAGCTCTGTGGGG | 12449 |
rs108550024 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | GRCm38.p3 | 17:24242931 | GGCCTTGGGGCTAAG[A/G]ATTCCCGTGGGACCA | 12449 |
rs108558120 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24228051 | CTCAGAAGTACAAGC[A/G]AGGTGGGCTGGGCTG | 12449 |
rs108559805 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24243790 | GGCATCTGTGGGCAT[C/T]GCACACAGGTAGTGC | 12449 |
rs108560658 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24245224 | TATGATAACCTTGAC[A/G]ATACGTTTTAAAAAC | 12449 |
rs108565331 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24245388 | TGGGAGAGGGGGAGT[A/G]GCACCTAAGATTCTC | 12449 |
rs108567028 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24233688 | TAGGAACCCTAGTAC[A/G]CAAGCGAGCCTAGGA | 12449 |
rs108570321 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24243131 | GATCCAAATTAGGAA[A/C]GGGGGTGACTTCCTT | 12449 |
rs108574285 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24237310 | CAGCCACACAGTACA[C/T]ACGGCCAGCCTGGGC | 12449 |
rs108584039 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24244076 | ACACGCTCTGGGGCT[A/G]CTGGGGGTCTCAGAC | 12449 |
rs108585887 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24233304 | TGGCGGTGACAGGAA[A/G]AAGAACCACTCATGG | 12449 |
rs108591442 | snp | G/T | | | intron-variant | Ccnf | Mm_Celera | 17:24243791 | GCATCTGTGGGCATT[G/T]CACACAGGTAGTGCA | 12449 |
rs108596709 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24231063 | GCCCTGGCTGTCCTG[A/G]AACTCACTCATAGAC | 12449 |
rs108602527 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24230657 | CCACGGCATGGAACG[A/G]GCACACACATGCACA | 12449 |
rs108604566 | snp | A/G | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24251660 | CCGGAGGCAGAGAGG[A/G]CTGGTCTTCTCCCTC | 12449 |
rs108604630 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24229608 | CAGACAGCTCAGTAG[A/G]CAAAGATGCTTGCTG | 12449 |
rs108609394 | snp | A/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | Mm_Celera | 17:24235726 | GGGGCTTCCCAATAG[A/T]ACTAGGATGGCTGCG | 12449 |
rs108613948 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24233693 | ACCCTAGTACACAAG[C/T]GAGCCTAGGAAGGAG | 12449 |
rs108623066 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24244065 | CTGTCCCAAGGACAC[A/G]CTCTGGGGCTGCTGG | 12449 |
rs108628130 | snp | A/T | | | intron-variant | Ccnf | Mm_Celera | 17:24243567 | CATGAGATGTCTCCA[A/T]CTGCCAACTCCAAAG | 12449 |
rs108643144 | snp | A/T | | | intron-variant | Ccnf | Mm_Celera | 17:24225272 | AAGAACTGGGCAAGG[A/T]TAGGCTTCAGAATAG | 12449 |
rs108653338 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24228616 | AGGTCTCGTGGAAGA[A/G]CGTCCAGTGCTCTGA | 12449 |
rs108656328 | snp | C/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24228901 | TGTAACACACACATA[C/G]ACACACACACACACA | 12449 |
rs108664186 | snp | G/T | | | intron-variant | Ccnf | Mm_Celera | 17:24243627 | CTTGTGGGCTTCAGG[G/T]AGACAGGACCATGCC | 12449 |
rs108667241 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24241736 | GTCACTGTCTTCCAA[C/T]ACAGCAGAAGTCGGC | 12449 |
rs108673701 | snp | A/G | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24252641 | TTATTTATTGGAGGC[A/G]GGTTTTGTTGGTTTT | 12449 |
rs108686825 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24248167 | CTTGATGTGTCTGCC[A/G]CACATCTGTGCTTGG | 12449 |
rs108687936 | snp | A/T | | | intron-variant | Ccnf | Mm_Celera | 17:24230825 | ACCACAACCATCTGT[A/T]ATGGGATCCAATGCC | 12449 |
rs108700157 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | Mm_Celera | 17:24235740 | GTACTAGGATGGCTG[C/T]GCACAGAACCTCTGG | 12449 |
rs108701833 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24228489 | GTTTGCCTGCAGGTA[C/T]ATCTGCACCACAAGT | 12449 |
rs108720587 | snp | G/T | | | intron-variant | Ccnf | Mm_Celera | 17:24229927 | AGCCACCAAGTGGTT[G/T]CTGGGATTTGAACTC | 12449 |
rs108732547 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24233463 | GATTGCTATGGGAGG[A/G]CTCAGCTCACTGTGG | 12449 |
rs108738511 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24242504 | GGTCCTTCAGGAAGC[C/T]TGAATTCTGACCCTC | 12449 |
rs108740743 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24240185 | TTCATCCCAGGGCCA[C/T]GTGAAACCATGTTTA | 12449 |
rs108743931 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24229061 | TGTTGGTATCCGCTG[C/T]TGGGTACAGGCTAAG | 12449 |
rs108764536 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24230942 | TCCATACACAGTATA[C/T]ACACTTGAAAAACTA | 12449 |
rs108776251 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | Mm_Celera | 17:24235647 | CTTACTGGCCCCAGT[A/G]ATCTGTTTTTAGAAA | 12449 |
rs108797506 | snp | C/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24231019 | CATTTCTTTCTTTTT[C/G]TTTTTTCCAGACAGA | 12449 |
rs108798056 | snp | A/T | | | intron-variant | Ccnf | Mm_Celera | 17:24228451 | TACAAAAGTTTATTT[A/T]TTTTTGTATCATGTG | 12449 |
rs108814230 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24227648 | TAAAGGTGGAGGGCG[A/G]AGACACCGAGCCTAT | 12449 |
rs108867427 | snp | G/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24230112 | GCTAGGTGATAAAGC[G/T]AAAGTCTGATGGTAG | 12449 |
rs108876735 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24228766 | TACAGTACATTCTGA[A/C]CATGGTTTCCCCTCC | 12449 |
rs108880903 | snp | A/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24233370 | CATGACCTTCATCCC[A/T]GTGGGCCGGATGTTC | 12449 |
rs108886170 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24248088 | CCCTCTTCTGGTGTG[C/T]CTGAGGACAGCTACA | 12449 |
rs108894009 | snp | G/T | | | intron-variant | Ccnf | Mm_Celera | 17:24236696 | GTGGTGACCAACTGT[G/T]AACTCCAGCTGTTGT | 12449 |
rs108901590 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | GRCm38.p3 | 17:24235084 | AAAAACCTGGGGAAC[A/G]AGGCCATAAAAAACC | 12449 |
rs108902173 | snp | A/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | Mm_Celera | 17:24235687 | TGGGCTATCAAGAGT[A/T]GGATTAAAGGCATGC | 12449 |
rs108908908 | snp | C/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24237565 | CCTCTTGGAGAGCAG[C/G]CGGAGCTCTTAACCA | 12449 |
rs108915941 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | GRCm38.p3 | 17:24235496 | GTGGTAAGTATGTGC[A/G]GTTGCATGTATGACA | 12449 |
rs108918754 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24228672 | ACCCACCCCAACTCT[C/T]CTTTCTATGGTCCAT | 12449 |
rs211703649 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24239701 | ACAGACAAGCATATG[C/T]ATATAAATAAGTAAA | 12449 |
rs211796179 | in-del | -/AAACCCATAC | | | intron-variant | Ccnf | Mm_Celera | 17:24228744 | TTTCTTTCTTTTTAA[-/AAACCCATAC]AGTACATTCTGACCA | 12449 |
rs211859503 | snp | G/T | | | intron-variant | Ccnf | Mm_Celera | 17:24246613 | ACACCATTCCTCAGC[G/T]TGAGTATAAATTGCT | 12449 |
rs211971884 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24227974 | AGCCATCAGCAGGTC[A/G]TACAGACGAAGGAGG | 12449 |
rs212008091 | snp | A/G/T | | | intron-variant | Ccnf | Mm_Celera | 17:24227563 | CTCCCTCTCTCTCTC[A/G/T]CACACACACACACAT | 12449 |
rs212027871 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24232825 | CGGTGTAGGAGGGCT[A/G]CACACAGCCCTCCCG | 12449 |
rs212201228 | snp | C/G | | | intron-variant | Ccnf | Mm_Celera | 17:24248012 | TGCTCTTGCAGAGGT[C/G]CTGAGTTCAATTCCC | 12449 |
rs212286348 | in-del | -/G | | | upstream-variant-2KB | Ccnf | GRCm38.p3 | 17:24251862 | GCGATGTGTTCACTC[-/G]AGTACATGTTCCGTA | 12449 |
rs212318135 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24241830 | CTCTGGAAGAGCAGT[C/T]GGTGCTCTTAACTGC | 12449 |
rs212338297 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24233790 | GAGTAAGAAAATGCA[A/G]ACTACATTTTGAAAA | 12449 |
rs212419179 | in-del | -/GGGAAG | | | intron-variant | Ccnf | Mm_Celera | 17:24245034 | ACAAATAAAGGGTGA[-/GGGAAG]GGGAAGGGGACACAG | 12449 |
rs212482432 | in-del | -/GGCAACGGCGT | | | intron-variant | Ccnf | Mm_Celera | 17:24244346 | GGGCAGGCAGAGGAA[-/GGCAACGGCGT]GGCTGGAAGCAGGGG | 12449 |
rs212607895 | snp | C/T | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24251564 | TCTATTGGCTTATCG[C/T]TCGTGGTTGACCCGC | 12449 |
rs212692108 | in-del | -/AAC | | | intron-variant | Ccnf | GRCm38.p3 | 17:24229748 | ACATCCTATAATAAT[-/AAC]AACAACAATAATAAA | 12449 |
rs212941568 | snp | C/T | | | missense | Ccnf | Mm_Celera | 17:24226691 | GGCTGTACCTCTTCC[C/T]GGCTGATTTCCTCAT | 12449 |
rs212980531 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24226093 | ACAGACACAGGGCAG[A/G]CAGCTAACAAAGATA | 12449 |
rs213019619 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24231562 | CAGCCCAGCAGGGTT[C/T]TGGCCTAGGTGCTCA | 12449 |
rs213057634 | snp | A/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24230917 | TAAATAATTTTTTTT[A/T]AAAAAAGACTCCATA | 12449 |
rs213076359 | in-del | -/T | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24251700 | TCCTACCGTCCGGAG[-/T]TGGTCGTGGCTTACT | 12449 |
rs213176852 | in-del | -/A | | | intron-variant | Ccnf | GRCm38.p3 | 17:24227590 | CATATACACACACTC[-/A]CTCCTTCTTTGCAGA | 12449 |
rs213324415 | in-del | -/AGAAG | | | intron-variant | Ccnf | GRCm38.p3 | 17:24244783 | TGATGTTCTGAGGCA[-/AGAAG]AAAGACCTATGCTAA | 12449 |
rs213371939 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24228526 | GCCCACGGAGGCCAG[A/G]AGATGGCACGGGAAC | 12449 |
rs213404981 | in-del | -/AA | | | intron-variant | Ccnf | Mm_Celera | 17:24227205 | AAATCTGAATATAGT[-/AA]AAAAAAAAAAACTTT | 12449 |
rs213412762 | snp | A/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24228118 | GTGGTTAACTTTCTG[A/T]GGGGAGGGTCCAGGC | 12449 |
rs213471480 | in-del | -/AAA | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | GRCm38.p3 | 17:24241445 | AGCTTTATGACTCTT[-/AAA]AAAAAAACAAAACAA | 12449 |
rs213621110 | in-del | -/G | | | intron-variant | Ccnf | Mm_Celera | 17:24248604 | TGGTCACTGATGGCA[-/G]GTCCCAATACTCCAG | 12449 |
rs213835656 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24250512 | GCTCTTCAGATGAGC[C/T]CTTCTCCTCCACAGT | 12449 |
rs213922326 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24241089 | GGACGGTGGCAGTGG[C/T]GGCTCTCACCGCTCA | 12449 |
rs213940973 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24230190 | AGCCTCCTTTCTGAA[A/G]ACAGGGTCTTGGTAC | 12449 |
rs213961248 | in-del | -/AACCC | | | intron-variant | Ccnf | Mm_Celera | 17:24247304 | AAAAAAAAAACAAAA[-/AACCC]CAAAACAAAACAAAA | 12449 |
rs214094697 | in-del | -/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24229459 | CGGCAACCACATGGT[-/G]GCTCACAAACATCCG | 12449 |
rs214118426 | in-del | -/G | | | intron-variant | Ccnf | Mm_Celera | 17:24229572 | TTAAAAAAAAAAAAA[-/G]AAAGCCAACTCAGGG | 12449 |
rs214162963 | in-del | -/GTG | | | downstream-variant-500B, upstream-variant-2KB | Ccnf, 1600002H07Rik | Mm_Celera | 17:24222762 | AATGGGTTTGTACTT[-/GTG]GTTCAAGGGTATCTG | 12449 |
rs214214297 | in-del | -/TT | | | intron-variant | Ccnf | Mm_Celera | 17:24243444 | TATTTCCTGACTGAA[-/TT]TTTTTTTTTAATGAA | 12449 |
rs214214769 | in-del | -/GGC | | | intron-variant | Ccnf | Mm_Celera | 17:24226182 | ATGAATAAGGGTGTA[-/GGC]AGGGAGAGATCTGAA | 12449 |
rs214245929 | snp | C/G | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24242821 | GCAGATCTTTAAGCT[C/G]TAGGAAACTGGTATT | 12449 |
rs214296064 | in-del | -/C | | | intron-variant | Ccnf | GRCm38.p3 | 17:24224867 | TCAGATCATGTGTCA[-/C]CCGCATGCCACATCC | 12449 |
rs214314787 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24232712 | TGTAGGAGGGCTACA[C/T]ACAGCCCTCCCGGTG | 12449 |
rs214349587 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24232155 | ACAAGTGTCGGGTCC[A/C]GAAGAAGCCTGGGAC | 12449 |
rs214367595 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24239085 | TGGGGCAACAAGAAC[A/G]AGCTTTCCCCATTGT | 12449 |
rs214502743 | in-del | -/T | | | intron-variant | Ccnf | Mm_Celera | 17:24245211 | CACTTTCAGGGATAT[-/T]GATAACCTTGACGAT | 12449 |
rs214647369 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | Mm_Celera | 17:24235656 | CCCAGTGATCTGTTT[C/T]TAGAAATCAGATTAT | 12449 |
rs214847985 | snp | C/G | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24253142 | TGGCCCAGGGAGTGG[C/G]ACTATTAGAAAGTGT | 12449 |
rs215020270 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24240257 | CTATACCAGGGCCAC[A/G]TGAAACCATGCCTGT | 12449 |
rs215206969 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24247633 | TATAGCCCTGGCTGT[C/T]CTGGAACTCACTCTG | 12449 |
rs215291709 | snp | A/T | | | intron-variant | Ccnf | Mm_Celera | 17:24230914 | AAATAAATAATTTTT[A/T]TTAAAAAAAGACTCC | 12449 |
rs215358305 | in-del | -/C | | | intron-variant | Ccnf | GRCm38.p3 | 17:24231687 | GGCCTCAGCTTCCCG[-/C]CAACAGCCACCCCGC | 12449 |
rs215436192 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24248580 | CTAGGTAAGGAAGAG[C/T]CGGGTAAGATGGTCA | 12449 |
rs215612263 | snp | C/G | | | intron-variant | Ccnf | Mm_Celera | 17:24246770 | TTGGCTGCTCTTGCA[C/G]AGGACCTGGGTTTAG | 12449 |
rs215675337 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24250605 | TATTTCACAAAGGGC[C/T]CCCACATTACCCCCC | 12449 |
rs215680465 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24247476 | ACTTACAAATAATAA[A/G]TAATCTTTGGGCTGG | 12449 |
rs215681329 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24239719 | ATAAATAAGTAAAAA[A/C]TGAAAACAAAATAAA | 12449 |
rs215717908 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24240194 | GGGCCATGTGAAACC[A/G]TGTTTAATGTGGTCT | 12449 |
rs215922368 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24244095 | GGGGTCTCAGACAGC[A/G]GGCCTGGTCACTGGC | 12449 |
rs216161361 | snp | C/T | | | intron-variant, utr-variant-5-prime | Ccnf | Mm_Celera | 17:24251264 | CCGTTCCGTATGACC[C/T]ATCGCCTACCCGGCT | 12449 |
rs216219505 | snp | C/G | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | Mm_Celera | 17:24235562 | GGTTCTCTTCTTCCA[C/G]GACATAGGTCCTGGG | 12449 |
rs216249696 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24225593 | GGCCTTTTGGAGAGC[C/T]GGTTTAACACTGAAA | 12449 |
rs216251489 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | Mm_Celera | 17:24235040 | CAGACACAAGAAGGC[C/T]GGCAAAAGTCTCTCT | 12449 |
rs216322544 | in-del | -/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24243960 | AGCAACTCAAATAGA[-/T]TAAGGGTCTGGGAAG | 12449 |
rs216537996 | in-del | -/A | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | GRCm38.p3 | 17:24236331 | TAAGGTGCTGGGCTC[-/A]AAAATCTAGATCCTC | 12449 |
rs216630223 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24238331 | CATTTAAAGCTGTAG[A/C]TCCAAATTCATAAAC | 12449 |
rs216805785 | in-del | -/G | | | intron-variant | Ccnf | Mm_Celera | 17:24231693 | CAGCTTCCCGCAACA[-/G]CCACCCCGCCCCCCG | 12449 |
rs216881599 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24246647 | TCCTTAGGTTGTAGT[C/T]TTAGAATATTTGATT | 12449 |
rs216998489 | in-del | -/CAGTCAGGAACA | | | intron-variant | Ccnf | Mm_Celera | 17:24238658 | AAGCCATGAGCAAGC[-/CAGTCAGGAACA]CCCCATCCACAGCCT | 12449 |
rs217030883 | in-del | -/ATA | | | intron-variant | Ccnf | GRCm38.p3 | 17:24229803 | TATTGTAACTTTAAT[-/ATA]ATACCTTTTTTTTTT | 12449 |
rs217090532 | snp | G/T | | | downstream-variant-500B, upstream-variant-2KB | Ccnf, 1600002H07Rik | Mm_Celera | 17:24222911 | AAAGGGACCAGACCC[G/T]GCTGGTTTCTCCCCA | 12449 |
rs217124683 | snp | G/T | | | downstream-variant-500B, upstream-variant-2KB | Ccnf, 1600002H07Rik | Mm_Celera | 17:24222787 | TATCTGGGGCACTCC[G/T]GGTACTTTCTTCAGG | 12449 |
rs217160611 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24228941 | TAAAGACACAAACTC[A/G]GGAACCATAATATAC | 12449 |
rs217166694 | snp | C/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24228921 | ACACACACACACATA[C/G]ACCATAAAGACACAA | 12449 |
rs217203774 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24249763 | TGTTGGAAATTTTCT[A/G]ATCCAAGATCTACAT | 12449 |
rs217207019 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24228567 | GAGTTACAGGTGGTT[A/C]GGAGCCTCCATGCGG | 12449 |
rs217278379 | in-del | -/TTTGGGG | | | intron-variant | Ccnf | GRCm38.p3 | 17:24240066 | AAATAATGGTAGTCT[-/TTTGGGG]GGGGGGGCGGGGAGT | 12449 |
rs217440277 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | GRCm38.p3 | 17:24241630 | TTTTCTTTTCTTTTT[C/T]CTTTTTTTTTTCTTT | 12449 |
rs217574578 | snp | C/T | | | intron-variant, missense | Ccnf | Mm_Celera | 17:24251219 | CGCACTCCCGGGTCA[C/T]AGGGGCCCGAGTCCA | 12449 |
rs217611968 | snp | C/T | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24253050 | CAGGCTGACCTATAA[C/T]GTGAGGTCTGTCCTG | 12449 |
rs217619208 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24243637 | TCAGGGAGACAGGAC[A/C]ATGCCTGCTAAACAG | 12449 |
rs217621147 | in-del | -/C | | | intron-variant | Ccnf | Mm_Celera | 17:24250307 | CTCATGCTGCAGTGA[-/C]CCCCCAACCATAAAA | 12449 |
rs217841084 | snp | C/T | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24252350 | CATGTGGCACCACCA[C/T]CCAGCTACTTTGTTA | 12449 |
rs217874614 | in-del | -/TTTA | | | intron-variant | Ccnf | Mm_Celera | 17:24228444 | CTTTCTTTACAAAAG[-/TTTA]TTTATTTTTGTATCA | 12449 |
rs218071711 | in-del | -/AAT | | | intron-variant | Ccnf | GRCm38.p3 | 17:24230904 | ATCATAGAATAAATA[-/AAT]AATTTTTTTTAAAAA | 12449 |
rs218278405 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24232103 | GATCCTCAGACCCAG[C/T]AGGAGAGGCATGGCT | 12449 |
rs218324316 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24226132 | GTCACAACCCAACTA[C/T]GGTTTATGCCACAGC | 12449 |
rs218435693 | snp | A/C | | | intron-variant | Ccnf | GRCm38.p3 | 17:24228206 | CCAGCCAGCCAGTGC[A/C]GCGGGGAGGAGGAAG | 12449 |
rs218441153 | snp | A/C/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24250235 | GGTCTTCCACACTCA[A/C/G]CTTACAGTGCAAAAT | 12449 |
rs218468289 | snp | A/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24227667 | CACCGAGCCTATGAC[A/T]GTCACCTTGCTTCCT | 12449 |
rs218471126 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24250645 | GTCCTGCCTTCCTAC[C/T]TATAAATGCGCCTAT | 12449 |
rs218700454 | in-del | -/C | | | intron-variant | Ccnf | GRCm38.p3 | 17:24229071 | GCTGTTGGGTACAGG[-/C]CTAAGGTTAAGTGTG | 12449 |
rs218829120 | snp | A/T | | | intron-variant | Ccnf | Mm_Celera | 17:24229920 | GGTTGTGAGCCACCA[A/T]GTGGTTGCTGGGATT | 12449 |
rs218993366 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24225689 | AAGGGTAATCCTGTC[C/T]CCAATAGTTAAGTCA | 12449 |
rs219148560 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24245066 | TCTTGCGTATCCCAA[C/T]AGAAGTGAGCATGGC | 12449 |
rs219257713 | in-del | -/T | | | intron-variant | Ccnf | Mm_Celera | 17:24232358 | CCTCTCTGCGTCTCC[-/T]TTTCCTTCTTCTCTC | 12449 |
rs219290195 | in-del | -/TAAT | | | intron-variant | Ccnf | GRCm38.p3 | 17:24230906 | CATAGAATAAATAAA[-/TAAT]TTTTTTTAAAAAAAG | 12449 |
rs219376284 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24227646 | AGTAAAGGTGGAGGG[C/T]GAAGACACCGAGCCT | 12449 |
rs219393212 | in-del | -/AAAGGGGTAGCC | | | intron-variant | Ccnf | GRCm38.p3 | 17:24238742 | TCAGTGATGAACATG[-/AAAGGGGTAGCC]AAATAAACCCTTTCC | 12449 |
rs219475157 | snp | G/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24228619 | TCTCGTGGAAGAGCG[G/T]CCAGTGCTCTGACCA | 12449 |
rs219503676 | snp | C/T | | | intron-variant, downstream-variant-500B | Ccnf, Mir5134 | Mm_Celera | 17:24234166 | CCAAAGAGGTATAAT[C/T]GACATACAAAGGGTC | 12449 |
rs219531513 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24233643 | TTTCCTCACCAAGCT[A/G]CTTTTGATCATGGGG | 12449 |
rs219574607 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24230262 | GACCAGGACTCACAC[C/T]GTCCCTTAGCCCTCT | 12449 |
rs219701114 | snp | A/C | | | intron-variant | Ccnf | GRCm38.p3 | 17:24229018 | CAAACAAACAAAAAA[A/C]CACATATAAAAATAC | 12449 |
rs219703570 | in-del | -/C | | | intron-variant, nc-transcript-variant | Ccnf, Mir6965 | GRCm38.p3 | 17:24240943 | CAATAGCCTCCCTCT[-/C]CCGCTCCTAGACCCT | 12449 |
rs219825378 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24231105 | TGAACTCAGAAATTC[A/G]CCTGCCCTTGACTCC | 12449 |
rs219856539 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24237693 | GGAGACGCTGCCTGG[A/C]ACCCACAGACTTCAG | 12449 |
rs220025315 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24231651 | GCTTCCTGGTGCTTT[C/T]TCCACAGCAGTAGCG | 12449 |
rs220076854 | snp | C/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24231708 | GCCACCCCGCCCCCC[C/G]CCCGCCCCCCCCCCC | 12449 |
rs220081852 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24238532 | AAGATCCACAGGCTG[A/C]AAACCTGCTGCTCTA | 12449 |
rs220243572 | in-del | -/CACAGCCA | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24251822 | CCGATGCCGGGCAGC[-/CACAGCCA]CAGTCACAGTCTGCT | 12449 |
rs220532196 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24240307 | GAGGTCACATGAAAC[C/T]GTGCCTGTGGTCTAT | 12449 |
rs220565969 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24239838 | AAAGAATCCAGAGCT[C/T]GAAGTCACCTGTGCT | 12449 |
rs220575710 | in-del | -/TAG | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | Mm_Celera | 17:24234799 | GGTGATCTCAATCCC[-/TAG]TGCTCATAGGCAGTG | 12449 |
rs220579052 | in-del | -/G | | | intron-variant | Ccnf | Mm_Celera | 17:24232074 | CAGGGGCTACAAAGA[-/G]GGGGTCAGAACAGGA | 12449 |
rs220584601 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24233008 | GTGGACTGCTGCTCA[A/G]CCTTGGCAGAAGGGT | 12449 |
rs220618447 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24232502 | CTCTTTATGACTTTA[C/T]AGATGAGGGCTTTTT | 12449 |
rs220698401 | in-del | -/A | | | intron-variant | Ccnf | Mm_Celera | 17:24239978 | CTGAGAGGAACTCAG[-/A]ACTGCCCCACAGGTT | 12449 |
rs220731377 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24243111 | CTGCTCAGTCATCCT[C/T]TGCCGATCCAAATTA | 12449 |
rs220801279 | in-del | -/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24230569 | ATAGTGTCAAGCCTG[-/G]TGACTTAGAACTGAT | 12449 |
rs220983841 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | Mm_Celera | 17:24235206 | GCAAGAGAGAAAAGG[C/T]GCAATGATGTGGACT | 12449 |
rs221011586 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24243073 | CCTGGCCTGATTTGC[C/T]GAGCACCTCCTATTC | 12449 |
rs221068476 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | Mm_Celera | 17:24235802 | GATTATAGGCACATG[C/T]GACTCCCTCAGACCT | 12449 |
rs221125440 | in-del | -/A | | | intron-variant | Ccnf | GRCm38.p3 | 17:24229022 | CAAACAAAAAAACAC[-/A]TATAAAAATACGAAG | 12449 |
rs221132784 | in-del | -/AGCGG | | | intron-variant | Ccnf | Mm_Celera | 17:24232664 | AGGTGAGCTGCTGGA[-/AGCGG]GCACGGTGGAGGGCT | 12449 |
rs221538974 | snp | A/G | | | synonymous-codon | Ccnf | Mm_Celera | 17:24239919 | GCATCGTCCGGGGTC[A/G]GACATCTGTCAACAA | 12449 |
rs221567936 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24244450 | ACCACCAAAGGCTGA[A/G]GGAGACCAACACTCA | 12449 |
rs221597014 | in-del | -/AAC | | | intron-variant | Ccnf | Mm_Celera | 17:24226268 | CAGACAGGCTCGAGT[-/AAC]AACAACAACAACAAC | 12449 |
rs221799760 | snp | A/G | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24251750 | GCTTCCGGCCGAGGA[A/G]ACTGCATTTGGAGGC | 12449 |
rs221800729 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24243155 | CTTCCTTAGAACCTA[C/T]ATCCAAGTGTCAAGG | 12449 |
rs222008225 | snp | A/T | | | intron-variant | Ccnf | Mm_Celera | 17:24248935 | AAAAAAAAAAAACGA[A/T]TAAACCACGCAATTC | 12449 |
rs222305964 | snp | G/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24241311 | CAAGGCAGTGTGGAA[G/T]CCTCAGGCTCTCTGC | 12449 |
rs222373840 | in-del | -/CAGTCACCTTGCTTCCTCAGCATGGT | | | intron-variant | Ccnf | GRCm38.p3 | 17:24227666 | ACACCGAGCCTATGA[-/CAGTCACCTTGCTTCCTCAGCATGGT]CTGGGCACCACAGGA | 12449 |
rs222498989 | snp | C/T | | | missense, downstream-variant-500B | Ccnf, Mir6965 | Mm_Celera | 17:24240834 | ATTAAGCATCCCTGA[C/T]GAGAAGACTCTTCCA | 12449 |
rs222553384 | in-del | -/GAAC | | | intron-variant | Ccnf | Mm_Celera | 17:24236750 | AGCAATACAGTGAGT[-/GAAC]TCACTGTTAGGCTAG | 12449 |
rs222556876 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24248117 | CAGTGTGCTCATATA[C/T]ATAACATAAATAAAT | 12449 |
rs222580332 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24225741 | AGTGCAAACTGTGGC[C/T]TTCTCAGGAGGACCC | 12449 |
rs222591353 | snp | G/T | | | downstream-variant-500B | Ccnf | Mm_Celera | 17:24223083 | CAAGGGGTGGGAGTA[G/T]GAGTTTCCGGTTCTG | 12449 |
rs222621791 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24225314 | GCCCTGGGTCCTTCT[C/T]ATAACTGGCAGACTC | 12449 |
rs222691600 | in-del | -/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24233839 | CAGAGGCAAATCTAA[-/T]GCACAGCTTGAGAAA | 12449 |
rs222809282 | snp | A/T | | | downstream-variant-500B | Ccnf | Mm_Celera | 17:24223169 | TCTGCCTGCCGGGAC[A/T]GTCGGGAGAGGCACT | 12449 |
rs222912062 | snp | G/T | | | intron-variant | Ccnf | Mm_Celera | 17:24239281 | ACTAAGTAACCAACA[G/T]GGGCCCCACACACCC | 12449 |
rs223079318 | snp | C/G | | | intron-variant | Ccnf | Mm_Celera | 17:24245473 | TCAAATTCCTATACA[C/G]CAAACACTTACTGGG | 12449 |
rs223107326 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24244422 | TTCAGGGGACACGAG[C/T]CAGCACACAAACACC | 12449 |
rs223127875 | snp | A/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24225846 | CACTGCTGCCTCCTC[A/T]CATCAGAAGACCGGT | 12449 |
rs223304666 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24225445 | TCAGGGCTAGAGAAC[C/T]ACAGAGCAGTCTGCC | 12449 |
rs223330717 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24226221 | ACTGTGTTCAGGTCC[A/G]TCTCCCTGAAAGTAA | 12449 |
rs223404801 | in-del | -/A | | | intron-variant | Ccnf | Mm_Celera | 17:24237632 | AAATGGCGCATCGAT[-/A]GGCCTTGGAGTCAGA | 12449 |
rs223417256 | in-del | -/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24245380 | AGCTATCCTGGGAGA[-/G]GGGGAGTAGCACCTA | 12449 |
rs223421666 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24249063 | ATTCTCAGCACTCAC[A/G]TGGCAGCTCACAATT | 12449 |
rs223426264 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24245326 | ATGGTGACTCTAGCC[A/G]TCCCAGCATTCTGGA | 12449 |
rs223534957 | snp | C/G | | | intron-variant | Ccnf | Mm_Celera | 17:24227266 | GTTTTTGGAGACAGG[C/G]TTTCTCTGTATAGCC | 12449 |
rs223699075 | in-del | -/CAGT | | | intron-variant | Ccnf | GRCm38.p3 | 17:24236742 | AGCCCCAGAGCAATA[-/CAGT]CAGTGAGTTCACTGT | 12449 |
rs223807885 | in-del | -/AC | | | intron-variant | Ccnf | GRCm38.p3 | 17:24227805 | CTGGTGGATTATTCT[-/AC]AGAGCTCAGACTTTA | 12449 |
rs223836234 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24250111 | CTTGCATAGCATAGA[C/T]TGGGAACTCAAATTA | 12449 |
rs223991355 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24249225 | AACAACACTAGGATT[A/G]GTATTGTTTCCATAT | 12449 |
rs224042696 | in-del | -/AATA | | | intron-variant | Ccnf | Mm_Celera | 17:24230896 | TACTCATAATCATAG[-/AATA]AATAAATAATTTTTT | 12449 |
rs224141188 | snp | G/T | | | intron-variant | Ccnf | Mm_Celera | 17:24229202 | GCCCACATAGAGTCT[G/T]AAGCACAGATGGTGG | 12449 |
rs224251134 | in-del | -/AA | | | intron-variant | Ccnf | Mm_Celera | 17:24248697 | AATCAATCAATTGAT[-/AA]AAAAAACCACTCTTG | 12449 |
rs224319204 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24225237 | GATGTGAGCCCTCAG[A/G]GCAGGGCATCAACTG | 12449 |
rs224407092 | in-del | -/A | | | intron-variant | Ccnf | Mm_Celera | 17:24248903 | GCAGGCAAAACACTC[-/A]AAAAAATAAAAATTA | 12449 |
rs224424496 | in-del | -/TT | | | upstream-variant-2KB | Ccnf | GRCm38.p3 | 17:24252571 | AGTTGATCAGTTGTC[-/TT]TTTTTTTTTTTTTGC | 12449 |
rs224504126 | snp | A/C | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24252482 | CTAACAATGAGCAAA[A/C]CCGCTGTCCATCACA | 12449 |
rs224619376 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24228903 | TAACACACACATAGA[C/T]ACACACACACACACA | 12449 |
rs224650300 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24230801 | GGGTACTGAGTTCAA[C/T]TCCCTGCAACCACAA | 12449 |
rs224665392 | snp | A/G | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24251854 | TCTGCTGAGCGATGT[A/G]TTCACTCGAGTACAT | 12449 |
rs224732846 | snp | A/C | | | intron-variant | Ccnf | GRCm38.p3 | 17:24227132 | GGAGATTGCTAAGTG[A/C]TGGCTAAAGAATGGG | 12449 |
rs224770108 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24232317 | TGTTCTCTTGGCCCG[A/G]CACCCCTCCGTCCAG | 12449 |
rs224828786 | in-del | -/AGGAA | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | GRCm38.p3 | 17:24235322 | GGCGAGGAACAGGAC[-/AGGAA]AGGTCTACTCCCCAC | 12449 |
rs224832768 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24227578 | TCACACACACACACA[C/T]ATACACACACTCCTC | 12449 |
rs224894611 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24247168 | GCAGTGGTGGCGCAC[A/G]CCTTTAATCCCAGCA | 12449 |
rs225003061 | in-del | -/TG | | | intron-variant | Ccnf | Mm_Celera | 17:24245379 | AGCTATCCTGGGAGA[-/TG]GGGGGAGTAGCACCT | 12449 |
rs225106515 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24250519 | AGATGAGCTCTTCTC[C/T]TCCACAGTGGGTTGT | 12449 |
rs225193076 | in-del | -/CTGTGGCTTT | | | intron-variant | Ccnf | GRCm38.p3 | 17:24225734 | GAGCACAGTGCAAAC[-/CTGTGGCTTT]TCAGGAGGACCCAGA | 12449 |
rs225198372 | in-del | -/CCCC | | | intron-variant | Ccnf | Mm_Celera | 17:24250614 | AGGGCCCCCACATTA[-/CCCC]CCCCCCCCCCCCAAG | 12449 |
rs225242349 | in-del | -/GACCC | | | intron-variant | Ccnf | GRCm38.p3 | 17:24232458 | CCAAAAAACAAAAAA[-/GACCC]GACCCATGAGCGACA | 12449 |
rs225257583 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24232714 | TAGGAGGGCTACACA[C/T]AGCCCTCCCGGTGTA | 12449 |
rs225330467 | in-del | -/C | | | intron-variant | Ccnf | Mm_Celera | 17:24250451 | CCCAATGGAGTCGCG[-/C]CCCACATGTTGAGAA | 12449 |
rs225336491 | snp | C/G | | | intron-variant | Ccnf | Mm_Celera | 17:24233371 | ATGACCTTCATCCCA[C/G]TGGGCCGGATGTTCT | 12449 |
rs225343922 | snp | C/G | | | intron-variant | Ccnf | Mm_Celera | 17:24228289 | GAGAGAAGGCAGAGG[C/G]AGCCAGCCCAGTGTC | 12449 |
rs225514156 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24227937 | GGCAGGTGACCAAGT[A/G]CAGGGAAAGGACACT | 12449 |
rs225626347 | snp | G/T | | | intron-variant | Ccnf | Mm_Celera | 17:24228585 | AGCCTCCATGCGGAT[G/T]CTAGGAACTGAGCCC | 12449 |
rs225632746 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24249471 | TAAAGATGATTTAAT[A/C]GTTACTGTCCTCTAT | 12449 |
rs225710384 | in-del | -/A | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24252454 | CCTCTGGAAGGTATT[-/A]AAAAAACTAAATCTA | 12449 |
rs225715654 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24237047 | TACAAGTTTTGCTCG[A/C]CACCAGGTCAAACAC | 12449 |
rs225872357 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24230743 | TCCATATAGGGGGCT[A/G]GAGAGATGGCTCAGC | 12449 |
rs225894307 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24230154 | CATCAGGGAAGCGCA[C/T]CTTACGGAGCCACCC | 12449 |
rs226042559 | in-del | -/A | | | intron-variant | Ccnf | Mm_Celera | 17:24250245 | CTCAGCTTACAGTGC[-/A]AAAATCACCCCTTCC | 12449 |
rs226183355 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24230562 | AAGGGCACATAGTGT[C/T]AAGCCTGATGACTTA | 12449 |
rs226331694 | in-del | -/CCTT | | | intron-variant | Ccnf | GRCm38.p3 | 17:24224443 | TGCTTAGGTAAAAGC[-/CCTT]TCTGTGAGTTTGACT | 12449 |
rs226398689 | snp | A/G | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24252706 | CCTGACACTGCTTAG[A/G]GTCATCTGAGGGAGA | 12449 |
rs226579455 | snp | G/T | | | intron-variant | Ccnf | Mm_Celera | 17:24231736 | CCCCCCCCCGTGACC[G/T]CAAACAGAAGAAACT | 12449 |
rs226590177 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24231514 | AGAGGGAGGAAAATG[C/T]CACGTCTCATCCATC | 12449 |
rs226672501 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24238883 | AGCCATATGGCTCTT[A/G]GAGAGCAAACTCTGG | 12449 |
rs226770853 | in-del | -/TT | | | intron-variant | Ccnf | GRCm38.p3 | 17:24247577 | TAAAAAAAGGAATTC[-/TT]TTTTTTTTTTTTTTT | 12449 |
rs226839986 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24229820 | TACCTTTTTTTTTTT[A/G]ATTTGTTTATTTATT | 12449 |
rs227134642 | snp | G/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24241074 | TGCTCTAAGCAGCAC[G/T]GACGGTGGCAGTGGT | 12449 |
rs227416320 | in-del | -/TAAG | | | intron-variant | Ccnf | Mm_Celera | 17:24239268 | AAGGCCAGAACTAAC[-/TAAG]TAACCAACAGGGGCC | 12449 |
rs227490627 | snp | C/G | | | intron-variant | Ccnf | Mm_Celera | 17:24239603 | TCAGGTGGCTCACAA[C/G]TGCCTGTAACTCCAC | 12449 |
rs227517050 | snp | G/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24245357 | GGCCGAGGCAGGCGC[G/T]AGAGGAAAGCTATCC | 12449 |
rs227550306 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24239067 | TATCTACCATCCATG[C/T]GGTGGGGCAACAAGA | 12449 |
rs227550348 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24246386 | ACTTCTGACATGATG[C/T]GTCCCACTTCACTGC | 12449 |
rs227706145 | in-del | -/CACTGCTGCCTCCTCACATCAGAAGACCG | | | intron-variant | Ccnf | Mm_Celera | 17:24225831 | AGGAGGTGAACCCCA[lengthTooLong]GTGACTGAAGCCAAG | 12449 |
rs227849503 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24238963 | TGTAAACCTCTGACA[A/G]TCTTAGACATGAACA | 12449 |
rs227878404 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24232045 | CCACTTGCTTCTGAC[C/T]ATCAAAGAGCATCCA | 12449 |
rs227945618 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24238297 | TAGAACACATTAATG[A/G]GACAAGTCCCCAATA | 12449 |
rs228180885 | in-del | -/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24232513 | TTTATAGATGAGGGC[-/T]TTTTTTTTTTAAGGT | 12449 |
rs228226796 | in-del | -/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24232817 | AGCCCTCCCGGTGTA[-/G]GAGGGCTACACACAG | 12449 |
rs228234784 | snp | C/G | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | Mm_Celera | 17:24235336 | CAGGAAAGGTCTACT[C/G]CCCACCCCCACCCCC | 12449 |
rs228392064 | snp | C/T | | | utr-variant-3-prime | Ccnf | Mm_Celera | 17:24223712 | TGGGTTTCACAGGTG[C/T]GCATGACAGCTGGGT | 12449 |
rs228443659 | in-del | -/AA | | | intron-variant | Ccnf | Mm_Celera | 17:24249414 | GGATCACTTAAAGGG[-/AA]AAAAAAAATTCACAA | 12449 |
rs228538046 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24224834 | CGATACTTTCCTCAG[C/T]ACAGTGCCAGATGGC | 12449 |
rs228814352 | in-del | -/GAGC | | | intron-variant | Ccnf | GRCm38.p3 | 17:24226436 | TACCATCTGTGAGGG[-/GAGC]AGCCATGGCGTGGCT | 12449 |
rs228872977 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24237986 | CTGAGGTTCGTGCTC[A/G]CGTGTCACTCATAAC | 12449 |
rs228931340 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24241734 | CTGTCACTGTCTTCC[A/G]ACACAGCAGAAGTCG | 12449 |
rs228969139 | snp | C/G | | | intron-variant | Ccnf | Mm_Celera | 17:24248381 | GGGTCTTTTTCTCTT[C/G]AAGTAACCATTGCAG | 12449 |
rs229006014 | in-del | -/AG | | | intron-variant | Ccnf | Mm_Celera | 17:24237676 | GATGTGCCAACACTT[-/AG]AGGAGACGCTGCCTG | 12449 |
rs229027036 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24247378 | AGGTCTGCTCTTCCG[A/C]AGGTCCTGAGTTCAA | 12449 |
rs229260077 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24244028 | TCTCAGCTGTGACAA[A/G]AAAAGGCTCAAGCTC | 12449 |
rs229288233 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24237313 | CCACACAGTACACAC[A/G]GCCAGCCTGGGCTTC | 12449 |
rs229293651 | in-del | -/A | | | intron-variant | Ccnf | Mm_Celera | 17:24227206 | AAATCTGAATATAGT[-/A]AAAAAAAAAACTTTT | 12449 |
rs229496635 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24246583 | TTCTGACACACAGCG[C/T]TTCCCTATTTCCCAA | 12449 |
rs229533040 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24249647 | GCCAGGGCTATACAG[A/G]AAAACCCTGTCTCAA | 12449 |
rs229548634 | in-del | -/G | | | intron-variant | Ccnf | Mm_Celera | 17:24245422 | TCCAATGCAAACCCA[-/G]CGCTCCAAAAACTGT | 12449 |
rs229563409 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24250254 | ACAGTGCAAAATCAC[A/C]CCTTCCTAGCACCGT | 12449 |
rs229564807 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24241843 | GTTGGTGCTCTTAAC[C/T]GCTGAGCCATCTCTC | 12449 |
rs229641589 | snp | A/C | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24251653 | AGCCCGCCCGGAGGC[A/C]GAGAGGGCTGGTCTT | 12449 |
rs229677275 | snp | G/T | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24252317 | CTGCCTCTGCCTCCC[G/T]AGTGCTGTGATTAAA | 12449 |
rs229710756 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | Mm_Celera | 17:24236212 | CAGCTCCCTAGGTCT[A/G]ACCTCTAGTCACTGA | 12449 |
rs229802091 | in-del | -/C | | | intron-variant | Ccnf | GRCm38.p3 | 17:24246303 | CACAACTGAACAAAG[-/C]TGCAGACAACTTGGC | 12449 |
rs229865704 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24239673 | AGGCATTGCATGCAC[A/G]GGGTATGTACATACA | 12449 |
rs229881582 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24240381 | CCCACACCAGATGAG[A/G]TCACATGAAACCGTG | 12449 |
rs230028900 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24226096 | GACACAGGGCAGGCA[A/G]CTAACAAAGATACTA | 12449 |
rs230061762 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24225726 | CCAAATACAGAGCAC[A/G]GTGCAAACTGTGGCT | 12449 |
rs230079308 | in-del | -/TTC | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | GRCm38.p3 | 17:24241629 | TTTTTCTTTTCTTTT[-/TTC]TTTTTTTTTTCTTTT | 12449 |
rs230143660 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24247222 | TTTCTGAGTTCAAGG[A/C]CAGCCTGGTCTACAG | 12449 |
rs230153241 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24245443 | CAAAAACTGTACAAC[A/G]GTCCAAAGATGACCT | 12449 |
rs230184436 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24239971 | CTATGTCCTGAGAGG[A/G]ACTCAGAACTGCCCC | 12449 |
rs230386962 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | GRCm38.p3 | 17:24241095 | TGGCAGTGGTGGCTC[C/T]CACCGCTCACCCGCC | 12449 |
rs230420371 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24228121 | GTTAACTTTCTGAGG[A/G]GAGGGTCCAGGCAGT | 12449 |
rs230569309 | in-del | -/A | | | intron-variant | Ccnf | GRCm38.p3 | 17:24244682 | ACGCATAGACATGTC[-/A]AGTCTCAGCATGGTA | 12449 |
rs230756673 | snp | A/C/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24229021 | ACAAACAAAAAAACA[A/C/G]ATATAAAAATACGAA | 12449 |
rs230811649 | snp | A/G | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24252825 | TCACCACCTCTGGTG[A/G]TGCCATCCCTAGGTA | 12449 |
rs230839031 | in-del | -/AACAAC | | | intron-variant | Ccnf | Mm_Celera | 17:24226267 | CAGACAGGCTCGAGT[-/AACAAC]AACAACAACAACAAC | 12449 |
rs230873773 | in-del | -/CTTCCCA | | | intron-variant | Ccnf | GRCm38.p3 | 17:24228789 | TCCCCTCCCCATCTC[-/CTTCCCA]CTTCCCACCCATTCA | 12449 |
rs230920797 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24225112 | CATAAACCCTGGCCA[C/T]AGATGGCAGCACCTG | 12449 |
rs231036351 | snp | A/G | | | synonymous-codon | Ccnf | Mm_Celera | 17:24224156 | GTATCCTGAGGTCGT[A/G]ATGTCCTTGGCCCGA | 12449 |
rs231057930 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24244118 | TCACTGGCAATGGGG[C/T]CACAGATTATAGGTT | 12449 |
rs231102106 | snp | C/G | | | intron-variant | Ccnf | Mm_Celera | 17:24231658 | GGTGCTTTCTCCACA[C/G]CAGTAGCGCTCAATG | 12449 |
rs231120614 | in-del | -/TTT | | | intron-variant | Ccnf | Mm_Celera | 17:24229809 | TAACTTTAATATACC[-/TTT]TTTTTTTTAATTTGT | 12449 |
rs231267230 | snp | A/C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24227542 | AAAATTTCTCTCTCT[A/C/T]TCTCTCTCCCTCTCT | 12449 |
rs231421214 | snp | G/T | | | intron-variant | Ccnf | Mm_Celera | 17:24232168 | CCCGAAGAAGCCTGG[G/T]ACAAGTCTCACTGAA | 12449 |
rs231877457 | in-del | -/TTGGGG | | | intron-variant | Ccnf | GRCm38.p3 | 17:24240067 | AATAATGGTAGTCTT[-/TTGGGG]GGGGGGGCGGGGAGT | 12449 |
rs231997795 | snp | C/T | | | synonymous-codon | Ccnf | Mm_Celera | 17:24243304 | GTAGAGGTAGGCAAT[C/T]CCCAACTTCACAGCA | 12449 |
rs232073517 | snp | A/T | | | intron-variant | Ccnf | Mm_Celera | 17:24233454 | ATCTTACTAGATTGC[A/T]ATGGGAGGGCTCAGC | 12449 |
rs232177804 | in-del | -/A | | | intron-variant | Ccnf | Mm_Celera | 17:24236903 | CATAGAAATGGGGGG[-/A]AAAGTAAAAAAAAAA | 12449 |
rs232266020 | snp | A/T | | | intron-variant | Ccnf | Mm_Celera | 17:24250305 | TTCCTCATGCTGCAG[A/T]GACCCCCAACCATAA | 12449 |
rs232507870 | in-del | -/AATTCCAGCTGCTGTGTGTGGTGACCAACTGTG | | | intron-variant | Ccnf | GRCm38.p3 | 17:24236640 | CCCATGAAAGTGCCA[lengthTooLong]GCTGTGTGTGGTGAC | 12449 |
rs232530891 | in-del | -/A | | | intron-variant | Ccnf | Mm_Celera | 17:24244906 | CTGTCCAAGGGAGGG[-/A]AGACCAGGAAGGAAT | 12449 |
rs232539718 | snp | G/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24242740 | ACTGACAGGGGGTTA[G/T]GGTAGGAGCCTCAGT | 12449 |
rs232826201 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24226415 | TGTCAAGAAGGAAAC[C/T]GAGAGCTACCATCTG | 12449 |
rs232882701 | in-del | -/A | | | intron-variant | Ccnf | Mm_Celera | 17:24249415 | GGATCACTTAAAGGG[-/A]AAAAAAATTCACAAG | 12449 |
rs232891830 | snp | A/G | | | intron-variant, downstream-variant-500B | Ccnf, Mir5134 | Mm_Celera | 17:24234058 | CTCTTCTTAGCAACT[A/G]GCATCCTTTGGATCA | 12449 |
rs232914531 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24241293 | GTCCTGTCCACCTCC[C/T]TCCAAGGCAGTGTGG | 12449 |
rs232949386 | snp | G/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24241997 | AGGTGAGAGCTCTCT[G/T]CTGAGCTGAAGCCCA | 12449 |
rs232954065 | in-del | -/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24236897 | TGAACACATAGAAAT[-/G]GGGGGAAAAGTAAAA | 12449 |
rs233060010 | snp | A/T | | | intron-variant | Ccnf | Mm_Celera | 17:24230915 | AATAAATAATTTTTT[A/T]TAAAAAAAGACTCCA | 12449 |
rs233111166 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24230468 | AGTTCTGGTAGTTCC[A/G]TAACATTTACCCAGA | 12449 |
rs233182188 | snp | C/G | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24252485 | ACAATGAGCAAACCC[C/G]CTGTCCATCACATTT | 12449 |
rs233232195 | snp | A/C | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24253172 | TGTTCCTGTTGTAGT[A/C]GGTGTGTCACTGTGG | 12449 |
rs233310410 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24244849 | ACCTTAGTACTCACT[A/G]GAGGCAGGGGTGGGC | 12449 |
rs233380098 | in-del | -/CCAGTGC | | | intron-variant | Ccnf | GRCm38.p3 | 17:24225925 | AGGTATCACCTAGCA[-/CCAGTGC]CCAACTGAAGGTTGC | 12449 |
rs233418135 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24226001 | AGGGAGGAGGCTGGG[C/T]GTCACAGGATCCACA | 12449 |
rs233562629 | snp | C/G/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24240243 | ACCGTGCCTGTGGTC[C/G/T]ATACCAGGGCCACAT | 12449 |
rs233581484 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24238343 | TAGCTCCAAATTCAT[A/G]AACCGCCTGCCTCAG | 12449 |
rs233603186 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24233377 | TTCATCCCAGTGGGC[A/C]GGATGTTCTGCCCAC | 12449 |
rs233782819 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24229506 | GCCCTCTTCTGGAGT[A/G]TCTGAAGACAGCTAC | 12449 |
rs233886056 | in-del | -/A | | | intron-variant | Ccnf | GRCm38.p3 | 17:24226966 | TTCAAACACCAACAC[-/A]ACATTGCAGTTTGAC | 12449 |
rs233954944 | snp | C/T | | | intron-variant, missense | Ccnf | Mm_Celera | 17:24251226 | CCGGGTCACAGGGGC[C/T]CGAGTCCATGCTCCT | 12449 |
rs234192963 | in-del | -/TTTTC | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | GRCm38.p3 | 17:24241627 | TTTTTTTCTTTTCTT[-/TTTTC]TTTTTTTTTTCTTTT | 12449 |
rs234503792 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24230851 | ATGCCCTCCTCTGAT[A/G]TGCCTGAAGACCTGA | 12449 |
rs234693367 | in-del | -/G | | | intron-variant | Ccnf | Mm_Celera | 17:24248768 | TCATCTAGAAGACCA[-/G]GGTTCAATTCCCAGC | 12449 |
rs234701409 | in-del | -/CT | | | intron-variant | Ccnf | GRCm38.p3 | 17:24250439 | TCGTGTGACCCCCCC[-/CT]AATGGAGTCGCGCCC | 12449 |
rs234782594 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24228429 | CTCCCCACCCGGTTT[C/T]TTTCTTTACAAAAGT | 12449 |
rs234812156 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24227075 | GAGTGGGCAAAGCCA[C/T]GGATGCGAAGCAATG | 12449 |
rs234944181 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24233659 | CTTTTGATCATGGGG[C/T]TTTTTCACAGAGATA | 12449 |
rs235102273 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24239753 | ACTCAGCTCTAGTCC[C/T]GGACCAATCTCACAG | 12449 |
rs235157382 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24228010 | CCAGCACTACCTCTG[A/G]GAGGAACACCGTGGG | 12449 |
rs235164417 | in-del | -/T | | | intron-variant | Ccnf | Mm_Celera | 17:24224584 | AAAAGCAGGTGAAAC[-/T]TGCCTAAGTCAGTGT | 12449 |
rs235194079 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24227567 | CTCTCTCTCTCTCAC[A/G]CACACACACATATAC | 12449 |
rs235254424 | snp | G/T | | | intron-variant | Ccnf | Mm_Celera | 17:24248038 | TTCCCAGCAACCACA[G/T]GGTGGCTCACAACCA | 12449 |
rs235289527 | snp | A/T | | | intron-variant | Ccnf | Mm_Celera | 17:24248821 | CTTCTGAAACTCAAG[A/T]CCCCAGGGATCAAAC | 12449 |
rs235473244 | snp | A/T | | | intron-variant | Ccnf | Mm_Celera | 17:24250081 | GTGACTATCAGCATA[A/T]GGTTGACCAAGGGAC | 12449 |
rs235481814 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | Mm_Celera | 17:24235657 | CCAGTGATCTGTTTT[C/T]AGAAATCAGATTATT | 12449 |
rs235640538 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24250651 | CCTTCCTACTTATAA[A/G]TGCGCCTATCTTTCT | 12449 |
rs235645886 | in-del | -/T | | | intron-variant | Ccnf | Mm_Celera | 17:24225798 | GATGCAGTGCAGATA[-/T]TTTGTAGCAGGTTTT | 12449 |
rs235656301 | snp | A/T | | | intron-variant | Ccnf | Mm_Celera | 17:24243678 | CTTTTTAGGATGATA[A/T]AAGTTGGACAGTGTT | 12449 |
rs235878695 | snp | A/T | | | intron-variant | Ccnf | Mm_Celera | 17:24238487 | TCACAATATAAATAT[A/T]TTTGGAGATAGAGGT | 12449 |
rs235924642 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24244989 | GTCTATACTACAAGT[C/T]CACGTTAGCAAAACC | 12449 |
rs235983826 | in-del | -/AA | | | intron-variant | Ccnf | GRCm38.p3 | 17:24247285 | AAACCCTGTCTCAAG[-/AA]AAAAAAAAAAAAACA | 12449 |
rs236299364 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24246894 | ACACATACAGATATG[C/T]AGGCAAAACACCCAG | 12449 |
rs236424954 | in-del | -/G | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24242347 | ACTGTGGGAGAAACA[-/G]GGCAAAGCTATGATG | 12449 |
rs236506785 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24231613 | CAGGGTTTCAGGGCA[A/G]CTAATGACACACCGC | 12449 |
rs236522405 | snp | C/G | | | intron-variant | Ccnf | Mm_Celera | 17:24239807 | GCCTAGGCGGTCCTG[C/G]CCCAAGGTTCAGAGA | 12449 |
rs236706602 | in-del | -/A | | | intron-variant | Ccnf | Mm_Celera | 17:24224866 | CTCAGATCATGTGTC[-/A]CCCGCATGCCACATC | 12449 |
rs236770656 | snp | C/G | | | intron-variant | Ccnf | Mm_Celera | 17:24228643 | CTGACCAACAGAGCC[C/G]TCCCTCCAGCTCTAC | 12449 |
rs236909434 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24228349 | AGTACCTGTCTACAC[C/T]AGCCCTGTACCAATG | 12449 |
rs236931635 | snp | C/T | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24251451 | TCCTACTGGTAGGAC[C/T]ACAGAGTTACGCCCC | 12449 |
rs236989395 | snp | G/T | | | intron-variant | Ccnf | Mm_Celera | 17:24250244 | CACTCAGCTTACAGT[G/T]CAAAATCACCCCTTC | 12449 |
rs237027305 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24225641 | TCAGTGATCCACCTC[C/T]AGTAGGTACCCATGT | 12449 |
rs237030322 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24225275 | AACTGGGCAAGGTTA[A/G]GCTTCAGAATAGGCC | 12449 |
rs237082083 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24245671 | AAGAAAGAAAGAAAG[A/G]AAGGAAGGAAGGAAG | 12449 |
rs237104133 | snp | A/T | | | downstream-variant-500B | Ccnf | Mm_Celera | 17:24223109 | TTCTGAGGTCAGATG[A/T]CCCAGGCCCCGTTGA | 12449 |
rs237166495 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24224811 | GGAAAACCCTTGACC[A/C]GAGTGTTCGATACTT | 12449 |
rs237247058 | snp | A/G | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24251995 | CCCTCCCCGAAGCCA[A/G]CATGCTCACTGTATC | 12449 |
rs237330938 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24237772 | TTGTAGCTTGGTGTG[C/T]ATGTGTATTTATGAC | 12449 |
rs237330961 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24230774 | AGTTAAGAGCACTGA[A/C]TGCTCTTCCAGGGGT | 12449 |
rs237340435 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | Mm_Celera | 17:24235087 | AACCTGGGGAACGAG[A/G]CCATAAAAAACCCCA | 12449 |
rs237381129 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24242133 | CCCAGGCCTTGCCAG[A/G]ACTTACTCTCTGTAA | 12449 |
rs237644477 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24227580 | ACACACACACACATA[C/T]ACACACACTCCTCCT | 12449 |
rs237696783 | snp | C/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24239095 | AGAACAAGCTTTCCC[C/G]ATTGTGGCAATCTGC | 12449 |
rs237751180 | snp | G/T | | | intron-variant | Ccnf | Mm_Celera | 17:24247334 | CAAAAAAGAATTCTT[G/T]TGCTGGAGAGATGGC | 12449 |
rs237952379 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24249895 | TGAAGGCTAGCTCAC[A/G]ACCAGTCAGTAAGAT | 12449 |
rs237989600 | snp | C/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24248292 | CTCTGGAAGAATGGT[C/G]AGTGCTTGTAACTGC | 12449 |
rs238231138 | in-del | -/CACCC | | | intron-variant | Ccnf | Mm_Celera | 17:24250432 | GAAAAGGTCGTGTGA[-/CACCC]CCCCCCCAATGGAGT | 12449 |
rs238430855 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24240265 | GGGCCACATGAAACC[A/G]TGCCTGTGATCTATC | 12449 |
rs238509831 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24226149 | GTTTATGCCACAGCA[C/T]GGAGCAGAGGGCACC | 12449 |
rs238641455 | in-del | -/CC | | | intron-variant | Ccnf | Mm_Celera | 17:24250510 | TGCTCTTCAGATGAG[-/CC]CTCTTCTCCTCCACA | 12449 |
rs238655629 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24231627 | AGCTAATGACACACC[A/G]CAGCCATGGCTTCCT | 12449 |
rs238718898 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24250626 | ATTACCCCCCCCCCC[C/T]AAGGTCCTGCCTTCC | 12449 |
rs239180229 | snp | C/G | | | intron-variant | Ccnf | Mm_Celera | 17:24225244 | GCCCTCAGGGCAGGG[C/G]ATCAACTGGAGGAAG | 12449 |
rs239182126 | snp | G/T | | | intron-variant | Ccnf | Mm_Celera | 17:24227275 | GACAGGGTTTCTCTG[G/T]ATAGCCCTGGCTGTC | 12449 |
rs239184203 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24233068 | TGACTGCTGAGAAGA[A/C]CTGGGATGTGAGATT | 12449 |
rs239288895 | snp | A/C | | | intron-variant | Ccnf | GRCm38.p3 | 17:24228938 | CCATAAAGACACAAA[A/C]TCAGGAACCATAATA | 12449 |
rs239322768 | snp | G/T | | | intron-variant | Ccnf | Mm_Celera | 17:24232536 | TTTAAGGTTTGTTTG[G/T]CTGTGCTGTGGTTCA | 12449 |
rs239356137 | snp | A/T | | | intron-variant | Ccnf | Mm_Celera | 17:24250555 | TATTTACTTCAGCAA[A/T]TCATTCTTCATTCAA | 12449 |
rs239447600 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24233141 | GGTCAGATGTTCCCC[A/C]CTGAAATCCACAGTC | 12449 |
rs239464992 | in-del | -/GTT | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | GRCm38.p3 | 17:24242636 | ATGAGAACAGCAGTG[-/GTT]GAAGCACCTTAGGAA | 12449 |
rs239511189 | snp | A/C | | | intron-variant | Ccnf | GRCm38.p3 | 17:24228069 | GTGGGCTGGGCTGGG[A/C]CCAGGAGCCCCGGAG | 12449 |
rs239551755 | snp | C/G | | | intron-variant | Ccnf | Mm_Celera | 17:24229914 | ACAGATGGTTGTGAG[C/G]CACCAAGTGGTTGCT | 12449 |
rs239590960 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | Mm_Celera | 17:24235765 | CTCTGGAACCCACTC[A/G]TCTCCACTTCCTCAG | 12449 |
rs239591068 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24229219 | AGCACAGATGGTGGG[C/T]AAATCACCAAAGCAG | 12449 |
rs239842536 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | Mm_Celera | 17:24235874 | CGAGCAAATTACTCA[C/T]TGAGGCCACCTCCAT | 12449 |
rs240044697 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24239173 | GATGGAACCAAGGGC[C/T]TAGCCTGCAAGTTCT | 12449 |
rs240256129 | snp | C/T | | | downstream-variant-500B, upstream-variant-2KB | Ccnf, 1600002H07Rik | Mm_Celera | 17:24222927 | GCTGGTTTCTCCCCA[C/T]GGAATCCAGCCACAA | 12449 |
rs240396075 | in-del | -/AGCAGG | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | Mm_Celera | 17:24235381 | GCTGAGGTTTAAAGC[-/AGCAGG]AGAACAGACTAGGAA | 12449 |
rs240431695 | snp | C/G/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24228952 | ACTCAGGAACCATAA[C/G/T]ATACACAAAGACCCC | 12449 |
rs240543887 | in-del | -/TGA | | | downstream-variant-500B, upstream-variant-2KB | Ccnf, 1600002H07Rik | Mm_Celera | 17:24222763 | ATGGGTTTGTACTTG[-/TGA]TTCAAGGGTATCTGG | 12449 |
rs240572158 | snp | G/T | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24253051 | AGGCTGACCTATAAC[G/T]TGAGGTCTGTCCTGC | 12449 |
rs240742248 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24233486 | CACTGTGGGTGGTGC[A/G]GTCCCTGGGCTGATG | 12449 |
rs240809681 | snp | A/T | | | intron-variant | Ccnf | Mm_Celera | 17:24232119 | AGGAGAGGCATGGCT[A/T]CAGAGCACAGACAAG | 12449 |
rs240866235 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24224479 | TCTCAAGCTGGAAAG[A/G]TTCCCCTTGATAACT | 12449 |
rs240992887 | snp | C/T | | | downstream-variant-500B | Ccnf | Mm_Celera | 17:24223202 | GCAGGACTAGATTTT[C/T]TCTTTTTTCAGTTGA | 12449 |
rs241083360 | in-del | -/A | | | intron-variant | Ccnf | GRCm38.p3 | 17:24230703 | ATGTAAAGTCAAGAT[-/A]AAAAAAAACTATCTT | 12449 |
rs241216963 | in-del | -/G | | | intron-variant | Ccnf | Mm_Celera | 17:24238592 | CAGCCCATTGTGGGT[-/G]GGGCCATCCCTGGGC | 12449 |
rs241335072 | snp | A/G | | | synonymous-codon | Ccnf | Mm_Celera | 17:24226777 | TTTGGGTGCATCATC[A/G]TGGAAACTGGAAATG | 12449 |
rs241502920 | snp | A/T | | | intron-variant | Ccnf | Mm_Celera | 17:24239293 | ACAGGGGCCCCACAC[A/T]CCCCTCCACTCCCAA | 12449 |
rs241554402 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24237972 | TCCAAGGACTCTCTC[C/T]GAGGTTCGTGCTCAC | 12449 |
rs241565254 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24238855 | CGAGCAGTCAGAGGA[C/T]ATCTTTTGGGACAGC | 12449 |
rs241623304 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24239839 | AAGAATCCAGAGCTT[A/G]AAGTCACCTGTGCTT | 12449 |
rs241683500 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24248388 | TTTCTCTTGAAGTAA[A/C]CATTGCAGCGAGTTG | 12449 |
rs241685234 | snp | G/T | | | intron-variant | Ccnf | Mm_Celera | 17:24247136 | AGCTCTTCTTGGACA[G/T]TTAAGAATTCTTGCG | 12449 |
rs241720049 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24241002 | CACGGCAGAAATGAG[A/G]CTGAGAAGCAGCCAG | 12449 |
rs241720179 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24249141 | CATGCAGACAAAACA[C/T]AAATGCATATGAAAT | 12449 |
rs241767693 | in-del | -/CACACACACAAATACAC | | | intron-variant | Ccnf | Mm_Celera | 17:24243854 | AAATAAATCTTAAAA[-/CACACACACAAATACAC]AAATACACACACACA | 12449 |
rs241932786 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24241480 | ACAAGCATGATTCTC[C/T]GCAGACATTTCTCCC | 12449 |
rs242073592 | snp | A/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24241339 | TGCCAGGGACCCACC[A/T]CAGGGCAAGGCGTGG | 12449 |
rs242257170 | in-del | -/A | | | intron-variant | Ccnf | Mm_Celera | 17:24238993 | ACAATATTCTGTGAC[-/A]AGAGATCAGCCAGGA | 12449 |
rs242257217 | in-del | -/C | | | intron-variant | Ccnf | Mm_Celera | 17:24249855 | TCAAGAAGGTACTTT[-/C]TGGGGCCAAGAAACT | 12449 |
rs242305212 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24229895 | GAGGGAGTCAGATCT[C/T]GTTACAGATGGTTGT | 12449 |
rs242310944 | in-del | -/TGTG | | | intron-variant | Ccnf | GRCm38.p3 | 17:24249078 | GTGGCAGCTCACAAT[-/TGTG]TGTAACTCCAGTTCC | 12449 |
rs242390791 | in-del | -/C | | | intron-variant | Ccnf | Mm_Celera | 17:24230992 | CCATCACCCAGAAAA[-/C]CCCCCATGCCTCATT | 12449 |
rs242433831 | snp | G/T | | | intron-variant, downstream-variant-500B | Ccnf, Mir5134 | Mm_Celera | 17:24234179 | ATCGACATACAAAGG[G/T]TCAACTCTGCCATCC | 12449 |
rs242441264 | in-del | -/TT | | | intron-variant | Ccnf | Mm_Celera | 17:24236708 | TGTTAACTCCAGCTG[-/TT]GTGTGAGGCTGGGTT | 12449 |
rs242511160 | in-del | -/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24247578 | TAAAAAAAGGAATTC[-/T]TTTTTTTTTTTTTTG | 12449 |
rs242525398 | snp | A/C | | | intron-variant | Ccnf | GRCm38.p3 | 17:24225540 | CCCATGTTACCCTGG[A/C]GGTCTCTTTGGAGGC | 12449 |
rs242549088 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24225447 | AGGGCTAGAGAACTA[C/T]AGAGCAGTCTGCCTC | 12449 |
rs242619899 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24232839 | TACACACAGCCCTCC[C/T]GGTGTAGGTGGGCTA | 12449 |
rs242697423 | in-del | -/T | | | intron-variant | Ccnf | Mm_Celera | 17:24233539 | GGCCCAGCAAGACAC[-/T]GAGCAAGCCACTATG | 12449 |
rs242704046 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24225853 | GCCTCCTCACATCAG[A/G]AGACCGGTGACTGAA | 12449 |
rs242742822 | in-del | -/AC | | | intron-variant | Ccnf | GRCm38.p3 | 17:24249163 | TATGAAATTTTAAAA[-/AC]ACACACACACACACA | 12449 |
rs242836050 | in-del | -/C | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | GRCm38.p3 | 17:24234698 | GCTGGTGGGTTCACA[-/C]ATCTCTGCAGCCTGT | 12449 |
rs242973307 | snp | A/G/T | | | intron-variant | Ccnf | Mm_Celera | 17:24227561 | CTCTCCCTCTCTCTC[A/G/T]CTCACACACACACAC | 12449 |
rs243094857 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24232724 | ACACACAGCCCTCCC[A/G]GTGTAGGAGGGCTAC | 12449 |
rs243186686 | snp | C/G | | | downstream-variant-500B, upstream-variant-2KB | Ccnf, 1600002H07Rik | Mm_Celera | 17:24222739 | GGATGGAACAGAAAA[C/G]AGAGAGCTAATGGGT | 12449 |
rs243220615 | snp | A/C | | | intron-variant | Ccnf | GRCm38.p3 | 17:24228907 | ACACACATAGACACA[A/C]ACACACACACATACA | 12449 |
rs243221788 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24238919 | AGGCTTGGTAGCAAG[C/T]GATGAGCCATCTTAC | 12449 |
rs243262216 | in-del | -/T | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24252043 | GGATAGCAAGACCTC[-/T]TAGTGGGTCTGAGAC | 12449 |
rs243309484 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24249564 | CCATTCCCCAGCACT[C/T]GGGAGGCAGAGGCAG | 12449 |
rs243416977 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24250520 | GATGAGCTCTTCTCC[C/T]CCACAGTGGGTTGTT | 12449 |
rs243494855 | in-del | -/ACACACACACACACAC | | | intron-variant | Ccnf | GRCm38.p3 | 17:24224645 | CTGCAGTACACACAT[-/ACACACACACACACAC]ACACACACACACACA | 12449 |
rs243500584 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24233820 | AGCGCCTTCCACATC[A/G]CTTCCAGAGGCAAAT | 12449 |
rs243538511 | snp | C/G | | | utr-variant-3-prime | Ccnf | Mm_Celera | 17:24223672 | TGCTCCCGGAGACAA[C/G]AGGACACAGAAGGGT | 12449 |
rs243628934 | snp | C/G | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | Mm_Celera | 17:24235381 | GGCTGAGGTTTAAAG[C/G]AGAACAGACTAGGAA | 12449 |
rs243636181 | in-del | -/G | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | Mm_Celera | 17:24235363 | CCCCAAGAAGGGTCA[-/G]GGGGCTGAGGTTTAA | 12449 |
rs243681286 | snp | C/G | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24252922 | CCTTGGTTGAGCTCC[C/G]GCTCTGACTTCCTTC | 12449 |
rs243730448 | snp | A/C | | | intron-variant, missense | Ccnf | Mm_Celera | 17:24251207 | GGGGATGCGACGCGC[A/C]CTCCCGGGTCACAGG | 12449 |
rs243755517 | snp | C/G | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24242478 | CTTCTCTAAGACAGG[C/G]CCCCTTCTGGGGTCC | 12449 |
rs243841930 | snp | A/G | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24252202 | ACTGTTTTCCAATTT[A/G]TTACTTTTTCTTTTC | 12449 |
rs243930030 | in-del | -/AA | | | intron-variant | Ccnf | Mm_Celera | 17:24229402 | ATGGCTCAGCGGTTG[-/AA]AGAACACCGACTGCT | 12449 |
rs243969260 | snp | C/G | | | intron-variant, downstream-variant-500B | Ccnf, Mir6965 | Mm_Celera | 17:24240547 | GTCTATCCCACACCA[C/G]ATGAGGTCACATGAA | 12449 |
rs244397895 | snp | A/T | | | intron-variant | Ccnf | Mm_Celera | 17:24238632 | TGGGTGCTATAAGGG[A/T]ACAGGCTGAGTAAGC | 12449 |
rs244442402 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24243999 | CAGGAGGAAAATCCT[A/G]TGCTGTGTTAGTTTC | 12449 |
rs244688161 | snp | A/G | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24251912 | CGAGAAAAGACAAGT[A/G]GTCTCTTGAGGGTGG | 12449 |
rs244743398 | in-del | -/TGGGC | | | intron-variant | Ccnf | GRCm38.p3 | 17:24228054 | GAAGTACAAGCGAGG[-/TGGGC]TGGGCTGGGCTGGGC | 12449 |
rs244773229 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24228617 | GGTCTCGTGGAAGAG[C/T]GTCCAGTGCTCTGAC | 12449 |
rs244781358 | snp | A/C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24230155 | ATCAGGGAAGCGCAT[A/C/T]TTACGGAGCCACCCC | 12449 |
rs244813515 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24229640 | TTAATTAAGCCTGAG[A/G]AGCGGAGTGCAAGTC | 12449 |
rs244845116 | snp | A/T | | | intron-variant | Ccnf | Mm_Celera | 17:24233651 | CCAAGCTGCTTTTGA[A/T]CATGGGGCTTTTTCA | 12449 |
rs244864471 | snp | C/T | | | synonymous-codon, downstream-variant-500B | Ccnf, Mir6965 | Mm_Celera | 17:24240875 | CGCCTGCTTCCTTTT[C/T]TCTTCGTCCTGGAGC | 12449 |
rs245043853 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24231953 | GAGCTGAGGGGCCAT[A/G]GCTCAGAAAGCCTCA | 12449 |
rs245046797 | in-del | -/T | | | intron-variant | Ccnf | Mm_Celera | 17:24250155 | AGAACATGGAGGCCA[-/T]GATCCATCCCAGAGC | 12449 |
rs245091161 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24248111 | CAGCTACAGTGTGCT[C/T]ATATATATAACATAA | 12449 |
rs245139943 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24232695 | ACACACAGCCCTCCC[A/G]GTGTAGGAGGGCTAC | 12449 |
rs245142479 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24239624 | GTAACTCCACTTCCA[A/G]GAGAGCCAATGAATA | 12449 |
rs245380248 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24226612 | CAGCACCTGTAGGGA[A/G]GACAGAGTGAAGCAC | 12449 |
rs245416933 | snp | A/T | | | intron-variant, nc-transcript-variant | Ccnf, Mir5134 | Mm_Celera | 17:24234604 | CTGCCAAGTCTGTTC[A/T]GCTTGAGCAAGTGGC | 12449 |
rs245840990 | in-del | -/GCTCTCACC | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24241091 | ACGGTGGCAGTGGTG[-/GCTCTCACC]GCTCACCCGCCTCCC | 12449 |
rs245985334 | in-del | -/AAAA | | | intron-variant | Ccnf | Mm_Celera | 17:24229559 | AAATAAATAAATCTT[-/AAAA]AAAAAAAAAGAAAGC | 12449 |
rs246027241 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24245566 | GTTCAAGGCTAGCCT[A/G]GTATATAGAGTGAGT | 12449 |
rs246069678 | snp | G/T | | | intron-variant | Ccnf | Mm_Celera | 17:24239461 | AATCGAAGAATTTCT[G/T]GGGTCTTCTTAAACA | 12449 |
rs246316303 | in-del | -/CTTCTCCCTCCAAGA | | | upstream-variant-2KB | Ccnf | GRCm38.p3 | 17:24251666 | GCAGAGAGGGCTGGT[-/CTTCTCCCTCCAAGA]CTTGTCCTACCGTCC | 12449 |
rs246420214 | in-del | -/AAAAAAC | | | intron-variant | Ccnf | GRCm38.p3 | 17:24247294 | CTCAAGAAAAAAAAA[-/AAAAAAC]AAAACAAAAAACCCC | 12449 |
rs246662520 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24249241 | GTATTGTTTCCATAT[A/G]GTAACTTACAGCTCG | 12449 |
rs246672926 | snp | A/G | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24252794 | GTATGATTGATGACT[A/G]AGAGGGTTCAGCCTC | 12449 |
rs246695264 | snp | C/G/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24226439 | CCATCTGTGAGGGAG[C/G/T]GAGCCATGGCGTGGC | 12449 |
rs246741486 | snp | C/G | | | intron-variant | Ccnf | Mm_Celera | 17:24248842 | GGGATCAAACACCCT[C/G]TTCTGGCCTTTGCAG | 12449 |
rs246782202 | snp | A/C | | | intron-variant | Ccnf | GRCm38.p3 | 17:24240246 | GTGCCTGTGGTCTAT[A/C]CCAGGGCCACATGAA | 12449 |
rs246932986 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24242677 | AACAAACCAACAACC[A/G]TGAACTTCGCATAAT | 12449 |
rs246974931 | snp | G/T | | | intron-variant | Ccnf | Mm_Celera | 17:24251056 | GCCCACGACTTCACA[G/T]ATAAGTAAAATCGTA | 12449 |
rs247018355 | in-del | -/C | | | intron-variant, downstream-variant-500B | Ccnf, Mir5134 | Mm_Celera | 17:24234147 | TGTGGGGGATACAGA[-/C]CCCCCAAAGAGGTAT | 12449 |
rs247027607 | in-del | -/AAATTATAT | | | intron-variant | Ccnf | Mm_Celera | 17:24243678 | TTTTTAGGATGATAA[-/AAATTATAT]AAGTTGGACAGTGTT | 12449 |
rs247083680 | snp | C/G | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24241922 | TACAACTACTCCCCC[C/G]ACCCCTCCTCTCTTC | 12449 |
rs247101987 | snp | A/G | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24252336 | GCTGTGATTAAAGGC[A/G]TGTGGCACCACCACC | 12449 |
rs247135659 | snp | G/T | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24252979 | AAGACAAATAAATTG[G/T]TTTTGGTCCTGTTGT | 12449 |
rs247148839 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24243692 | AAAAGTTGGACAGTG[C/T]TCATTTTGTTCACAA | 12449 |
rs247214471 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24244448 | ACACCACCAAAGGCT[A/G]AAGGAGACCAACACT | 12449 |
rs247292069 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24238090 | GGATTCAATTCCCAG[C/T]CCCCACATGGTAGCT | 12449 |
rs247295873 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24245345 | CAGCATTCTGGAGGC[C/T]GAGGCAGGCGCGAGA | 12449 |
rs247528933 | in-del | -/CCTA | | | intron-variant | Ccnf | Mm_Celera | 17:24246819 | TGGCTCAGAATCATC[-/CCTA]CCTAGCTCAGGTTCC | 12449 |
rs247535275 | in-del | -/AGGGGT | | | intron-variant | Ccnf | GRCm38.p3 | 17:24238744 | AGTGATGAACATGAA[-/AGGGGT]AGCCAAATAAACCCT | 12449 |
rs247565854 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24227145 | TGATGGCTAAAGAAT[A/G]GGGTTTCCTTTGAGG | 12449 |
rs247684738 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24240186 | TCATCCCAGGGCCAT[A/G]TGAAACCATGTTTAA | 12449 |
rs247780702 | snp | G/T | | | intron-variant | Ccnf | Mm_Celera | 17:24250950 | AGACGTTTTCACGGG[G/T]CAGATCCTGTGGCCT | 12449 |
rs247825285 | snp | C/G | | | intron-variant | Ccnf | Mm_Celera | 17:24247420 | CATCTGTAATGAGAT[C/G]TGATACCCTCATCTG | 12449 |
rs247825667 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24239705 | ACAAGCATATGTATA[C/T]AAATAAGTAAAAACT | 12449 |
rs248134388 | in-del | -/AACA | | | intron-variant | Ccnf | GRCm38.p3 | 17:24226292 | AACAACAACAACAAC[-/AACA]AAAGGCGATGCTTGG | 12449 |
rs248218511 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24229722 | ATCTCCACATGCACA[C/T]ATGTGCTCACACATC | 12449 |
rs248249246 | snp | G/T | | | intron-variant | Ccnf | Mm_Celera | 17:24229086 | GCTAAGGTTAAGTGT[G/T]GCTTGTATACCCTGT | 12449 |
rs248421222 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24232608 | AGCTCCTGTCCTATC[C/T]CCTTGACTGCATCTG | 12449 |
rs248471029 | snp | C/G | | | intron-variant | Ccnf | Mm_Celera | 17:24239557 | CTTACTGATCTCACA[C/G]ACGACCCAGGTTCAA | 12449 |
rs248548724 | in-del | -/TTC | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24242615 | TTAAGGATGAGAATA[-/TTC]TAAATGAGAACAGCA | 12449 |
rs248573857 | snp | A/G | | | synonymous-codon | Ccnf | Mm_Celera | 17:24224183 | CCGATCTCCCCGATT[A/G]CAGAGAAGGGGCCTG | 12449 |
rs248613642 | snp | G/T | | | intron-variant | Ccnf | Mm_Celera | 17:24226320 | GCTTGGGAACAGGCC[G/T]CGGCCAAGCCCAAGC | 12449 |
rs248638712 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24231689 | GCCTCAGCTTCCCGC[A/C]ACAGCCACCCCGCCC | 12449 |
rs248747925 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24228208 | AGCCAGCCAGTGCCG[C/T]GGGGAGGAGGAAGGA | 12449 |
rs248852252 | snp | A/T | | | intron-variant | Ccnf | Mm_Celera | 17:24227312 | CTCACTCTGTAGACC[A/T]GGCTGGCTTTGAACT | 12449 |
rs248924589 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24225765 | AGGACCCAGATCTCC[C/T]CCACTCCACAGAGAG | 12449 |
rs248945848 | in-del | -/C | | | intron-variant | Ccnf | Mm_Celera | 17:24243537 | ACAAAAGGTCAAGTA[-/C]TTATGATCTGTTTAC | 12449 |
rs248998351 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24231087 | CATAGACCAGGCTGG[C/T]CTTGAACTCAGAAAT | 12449 |
rs249001040 | snp | G/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | Mm_Celera | 17:24234767 | AATCCGAGTCAGCCC[G/T]CAGCCACCAAAGCAC | 12449 |
rs249062135 | in-del | -/T | | | intron-variant | Ccnf | Mm_Celera | 17:24239662 | TGGTCTCCACAGGCA[-/T]TTGCATGCACAGGGT | 12449 |
rs249064871 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24246638 | ATTGCTATCTCCTTA[A/G]GTTGTAGTCTTAGAA | 12449 |
rs249142295 | in-del | -/AAATACAC | | | intron-variant | Ccnf | GRCm38.p3 | 17:24243855 | AAATAAATCTTAAAA[-/AAATACAC]ACACACACACACACA | 12449 |
rs249170947 | snp | A/C | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | Mm_Celera | 17:24236374 | AACAAAACAAAAACC[A/C]AAAACCAAAAGTTGT | 12449 |
rs249183928 | in-del | -/C | | | intron-variant | Ccnf | Mm_Celera | 17:24250921 | ACAAGTGAAATCGCA[-/C]CCCCCAGGTCGTGAG | 12449 |
rs249225667 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24245177 | ACAACTCCAGCTGTC[C/T]ATCAAGCTGACGGTG | 12449 |
rs249375825 | snp | A/G | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24251531 | GCTACACCAGGACGC[A/G]AATTCAAACGCTGGC | 12449 |
rs249400589 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24250438 | GGTCGTGTGACCCCC[A/C]CAATGGAGTCGCGCC | 12449 |
rs249429492 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24228536 | GCCAGGAGATGGCAC[A/G]GGAACCTGTGGAACT | 12449 |
rs249449050 | snp | G/T | | | intron-variant | Ccnf | Mm_Celera | 17:24250041 | TAGTCACTATGGCCA[G/T]CTTACATTGTTTATA | 12449 |
rs249474901 | in-del | -/AAC | | | intron-variant | Ccnf | Mm_Celera | 17:24249669 | TGTCTCAAAAAACAA[-/AAC]AACAACAAAAAAGAT | 12449 |
rs249514079 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24230205 | AACAGGGTCTTGGTA[C/T]ACAGTCTAGGTGTCA | 12449 |
rs249616336 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24248993 | TTAAAAACATGCAAT[C/T]TGGGGCTGGAGAGAT | 12449 |
rs249802465 | in-del | -/TCCCACAAGCACCC | | | intron-variant | Ccnf | GRCm38.p3 | 17:24232967 | ACTCTGTTCCAGTGG[-/TCCCACAAGCACCC]TCCCCAGCGAATGTG | 12449 |
rs249892805 | in-del | -/C | | | upstream-variant-2KB | Ccnf | GRCm38.p3 | 17:24252918 | CCTGCCTTGGTTGAG[-/C]TCCGGCTCTGACTTC | 12449 |
rs249950579 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24228673 | CCCACCCCAACTCTT[C/T]TTTCTATGGTCCATC | 12449 |
rs249993846 | snp | C/T | | | intron-variant, downstream-variant-500B | Ccnf, Mir5134 | Mm_Celera | 17:24234348 | AGCACCTCAGCCCTG[C/T]CCGTTGGTCAAGGCT | 12449 |
rs250138657 | in-del | -/CTTC | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24241628 | TTTTTCTTTTCTTTT[-/CTTC]TTCTTTTTTTTTTCT | 12449 |
rs250354176 | in-del | -/CAAAA | | | intron-variant | Ccnf | GRCm38.p3 | 17:24247308 | AAAAACAAAAAACCC[-/CAAAA]CAAAACAAAACAAAA | 12449 |
rs250400874 | in-del | -/A | | | intron-variant | Ccnf | GRCm38.p3 | 17:24232932 | TTCTCTGCTGTCCAC[-/A]AGTACTAACAATCAG | 12449 |
rs250400911 | snp | A/G | | | intron-variant, downstream-variant-500B | Ccnf, Mir6965 | Mm_Celera | 17:24240429 | ACCAGATGAGGCCAC[A/G]TGAAACCGTGCCTGT | 12449 |
rs250472247 | in-del | -/AAAG | | | intron-variant | Ccnf | Mm_Celera | 17:24230545 | TATGGCTCCGTGGGC[-/AAAG]AAAGGGCACATAGTG | 12449 |
rs250527383 | snp | A/C | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24251774 | TGGAGGCGCCAACTC[A/C]AACACTGATGTGGAA | 12449 |
rs250542324 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | Mm_Celera | 17:24235073 | ACCAGGGAGTTAAAA[A/G]CCTGGGGAACGAGGC | 12449 |
rs250558987 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24244174 | CAGTCACGACTACAG[A/C]AGGGACATGAGTCAT | 12449 |
rs250701806 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24228126 | CTTTCTGAGGGGAGG[A/G]TCCAGGCAGTGAAAG | 12449 |
rs250929052 | in-del | -/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24227718 | GGAGGAAACTGGGTA[-/G]GCAAAAGCATAATAA | 12449 |
rs250990451 | snp | A/C/G | | | intron-variant | Ccnf | Mm_Celera | 17:24231712 | CCCCGCCCCCCGCCC[A/C/G]CCCCCCCCCCCCCCC | 12449 |
rs251024426 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24243937 | GAGGTCTCTACGTGG[A/C]CTTCACTAGCAACTC | 12449 |
rs251351299 | in-del | -/G | | | intron-variant | Ccnf | Mm_Celera | 17:24228018 | CCTCTGGGAGGAACA[-/G]CCGTGGGAGAGCAGC | 12449 |
rs251420584 | snp | A/T | | | intron-variant | Ccnf | Mm_Celera | 17:24230916 | ATAAATAATTTTTTT[A/T]AAAAAAAGACTCCAT | 12449 |
rs251563447 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24250383 | ATCTTAATGTAAATA[C/T]CTGATATGCAGGATG | 12449 |
rs251600604 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24242775 | CTCAGTCTGGAAGAG[A/G]CTGCCAAGGACAGGG | 12449 |
rs251731275 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24233387 | TGGGCCGGATGTTCT[A/G]CCCACAGGTTCCTAT | 12449 |
rs251917352 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24227697 | TCAGCATGGTCTGGG[A/C]ACCACAGGAGGAAAC | 12449 |
rs252089085 | snp | C/T | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24253125 | TCACGTTTGAATATG[C/T]TTGGCCCAGGGAGTG | 12449 |
rs252291090 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24246407 | ACTTCACTGCAGAAT[C/T]GGTTTTTAACACACA | 12449 |
rs252663938 | snp | C/T | | | intron-variant, downstream-variant-500B | Ccnf, Mir6965 | GRCm38.p3 | 17:24240694 | GAGGCTACATGAAAC[C/T]GTGCCTGAGGTCTAT | 12449 |
rs252748290 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24247165 | CGGGCAGTGGTGGCG[A/C]ACGCCTTTAATCCCA | 12449 |
rs252927441 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24243826 | CATACAAACACACAT[A/G]CATGCATAAAAATAA | 12449 |
rs253007311 | snp | G/T | | | intron-variant | Ccnf | Mm_Celera | 17:24250715 | GGCTGACCTCGGGCT[G/T]TCCATCAGGAGGTCT | 12449 |
rs253105542 | snp | A/T | | | intron-variant | Ccnf | Mm_Celera | 17:24239786 | TCCCTAAGTTCCCCG[A/T]TTAAAGCCTAGGCGG | 12449 |
rs253120844 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24233001 | AGCGAATGTGGACTG[A/C]TGCTCAGCCTTGGCA | 12449 |
rs253160986 | in-del | -/A | | | intron-variant | Ccnf | Mm_Celera | 17:24229476 | CTCACAAACATCCGT[-/A]ACAAAAAATCTGATG | 12449 |
rs253217126 | snp | A/T | | | intron-variant | Ccnf | Mm_Celera | 17:24230909 | AGAATAAATAAATAA[A/T]TTTTTTTAAAAAAAG | 12449 |
rs253251899 | in-del | -/T | | | intron-variant | Ccnf | Mm_Celera | 17:24245210 | ACACTTTCAGGGATA[-/T]TGATAACCTTGACGA | 12449 |
rs253258397 | in-del | -/C | | | intron-variant | Ccnf | Mm_Celera | 17:24247149 | ATTTAAGAATTCTTG[-/C]CGGGCAGTGGTGGCG | 12449 |
rs253290945 | in-del | -/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24232507 | ATGACTTTATAGATG[-/G]GGGCTTTTTTTTTTT | 12449 |
rs253440189 | snp | C/T | | | downstream-variant-500B, upstream-variant-2KB | Ccnf, 1600002H07Rik | Mm_Celera | 17:24222867 | AGCTGCCTCATAAAT[C/T]ACAAGGCAAAGCATT | 12449 |
rs253455640 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24241632 | TTCTTTTCTTTTTTC[-/T]TTTTTTTTTCTTTTA | 12449 |
rs253467445 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24243028 | CCAAGGAAGGAAGCC[A/G]TCTATGTCCATGCAG | 12449 |
rs253547315 | snp | C/G | | | intron-variant | Ccnf | Mm_Celera | 17:24246595 | GCGTTTCCCTATTTC[C/G]CAACACCATTCCTCA | 12449 |
rs253568114 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24225555 | AGGTCTCTTTGGAGG[C/T]CCCTTCTGAAGGGGC | 12449 |
rs253605596 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24239676 | CATTGCATGCACAGG[A/G]TATGTACATACAGAC | 12449 |
rs253785945 | snp | C/G | | | intron-variant | Ccnf | Mm_Celera | 17:24228351 | TACCTGTCTACACCA[C/G]CCCTGTACCAATGTC | 12449 |
rs253805658 | in-del | -/AAAAAAA | | | intron-variant | Ccnf | GRCm38.p3 | 17:24229558 | AAATAAATAAATCTT[-/AAAAAAA]AAAAAAAAAAAAAGA | 12449 |
rs253933604 | snp | A/C | | | intron-variant | Ccnf | GRCm38.p3 | 17:24233670 | GGGGCTTTTTCACAG[A/C]GATAGGAACCCTAGT | 12449 |
rs253993447 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24249648 | CCAGGGCTATACAGG[A/G]AAACCCTGTCTCAAA | 12449 |
rs254014969 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24228656 | CCGTCCCTCCAGCTC[C/T]ACCCACCCCAACTCT | 12449 |
rs254108636 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24250245 | ACTCAGCTTACAGTG[A/C]AAAATCACCCCTTCC | 12449 |
rs254260251 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24249630 | GAGTGAGTTCCAGGA[C/T]AGCCAGGGCTATACA | 12449 |
rs254348434 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24225859 | TCACATCAGAAGACC[A/G]GTGACTGAAGCCAAG | 12449 |
rs254393503 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24225443 | GGTCAGGGCTAGAGA[A/G]CTACAGAGCAGTCTG | 12449 |
rs254436129 | in-del | -/ACCCTTG | | | intron-variant | Ccnf | GRCm38.p3 | 17:24224801 | GTTAGGTGGGGGAAA[-/ACCCTTG]ACCCGAGTGTTCGAT | 12449 |
rs254483736 | in-del | -/AAAAAAAA | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | GRCm38.p3 | 17:24235909 | CCAGGACAATGATTT[-/AAAAAAAA]AAAAAAAAAAAAAAA | 12449 |
rs254515003 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24233787 | GAAGAGTAAGAAAAT[A/G]CAAACTACATTTTGA | 12449 |
rs254617211 | snp | A/G | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24252939 | CTCTGACTTCCTTCA[A/G]TGATGGGTTGTGACC | 12449 |
rs254784434 | in-del | -/CCAG | | | intron-variant | Ccnf | GRCm38.p3 | 17:24229017 | CAAACAAACAAAAAA[-/CCAG]ACACATATAAAAATA | 12449 |
rs254841216 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24225384 | TGCAGGGCCTGACTG[C/T]AGTCTGTCTTTGGGC | 12449 |
rs255113251 | in-del | -/A | | | intron-variant | Ccnf | Mm_Celera | 17:24231697 | TCCCGCAACAGCCAC[-/A]CCCGCCCCCCGCCCG | 12449 |
rs255471074 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24226107 | GGCAGCTAACAAAGA[C/T]ACTACTCAAGTCACA | 12449 |
rs255494227 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24238770 | AATAAACCCTTTCCT[C/T]CCCAACTTGATTTTT | 12449 |
rs255546819 | snp | G/T | | | intron-variant | Ccnf | Mm_Celera | 17:24238278 | AAACAGCAAAAAGAT[G/T]AAATAGAACACATTA | 12449 |
rs255658193 | snp | C/G | | | intron-variant | Ccnf | Mm_Celera | 17:24245153 | ACTTTCTAAAGGCAT[C/G]TATACCTAACAACTC | 12449 |
rs255683921 | snp | G/T | | | intron-variant | Ccnf | Mm_Celera | 17:24247335 | AAAAAAGAATTCTTT[G/T]GCTGGAGAGATGGCT | 12449 |
rs255692231 | in-del | -/AAAAT | | | intron-variant | Ccnf | GRCm38.p3 | 17:24243854 | AAATAAATCTTAAAA[-/AAAAT]CACACACACACACAC | 12449 |
rs255700443 | snp | A/T | | | intron-variant | Ccnf | Mm_Celera | 17:24230790 | TGCTCTTCCAGGGGT[A/T]CTGAGTTCAATTCCC | 12449 |
rs255785183 | in-del | -/T | | | intron-variant | Ccnf | Mm_Celera | 17:24248529 | GGACTAAAAAAGCAC[-/T]TTCTGGACCATGCTG | 12449 |
rs255840436 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24228512 | CCACAAGTACTGGGG[C/T]CCACGGAGGCCAGGA | 12449 |
rs255929110 | in-del | -/TATTG | | | intron-variant, downstream-variant-500B | Ccnf, Mir5134 | Mm_Celera | 17:24234224 | TACTGGGATTGAAAT[-/TATTG]TATTAACACAGTTGA | 12449 |
rs255997295 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24248344 | CTGTCTTCTTGAGAC[A/G]CAAATTTTACCGGCA | 12449 |
rs256051506 | in-del | -/TGGGA | | | intron-variant | Ccnf | Mm_Celera | 17:24228069 | TGGGCTGGGCTGGGC[-/TGGGA]CCAGGAGCCCCGGAG | 12449 |
rs256165119 | snp | A/G | | | intron-variant | Ccnf | GRCm38.p3 | 17:24233293 | CTTGGGAGCTTTGGC[A/G]GTGACAGGAAAAAGA | 12449 |
rs256315957 | snp | G/T | | | intron-variant | Ccnf | Mm_Celera | 17:24239665 | GTCTCCACAGGCATT[G/T]CATGCACAGGGTATG | 12449 |
rs256425344 | snp | C/G | | | intron-variant | Ccnf | Mm_Celera | 17:24228341 | AGCAGCCCAGTACCT[C/G]TCTACACCAGCCCTG | 12449 |
rs256467327 | snp | C/G | | | intron-variant | Ccnf | Mm_Celera | 17:24233636 | CCCTGACTTTCCTCA[C/G]CAAGCTGCTTTTGAT | 12449 |
rs256535051 | snp | G/T | | | intron-variant | Ccnf | Mm_Celera | 17:24249967 | CTAACATTAGCTGAG[G/T]TTACCCTTGAACTCC | 12449 |
rs256731918 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24250643 | AGGTCCTGCCTTCCT[A/G]CTTATAAATGCGCCT | 12449 |
rs256774136 | snp | A/T | | | intron-variant | Ccnf | Mm_Celera | 17:24243418 | AATCACAGCCCTTGA[A/T]GTTGAAAAGTTTATT | 12449 |
rs256879223 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24232006 | CTCCAGACTCAGGTG[A/G]CAAAAGGAAGCTATG | 12449 |
rs256886018 | in-del | -/TCCCCACCCACCC | | | intron-variant | Ccnf | Mm_Celera | 17:24228402 | CGTACCACTTCCACA[-/TCCCCACCCACCC]TCCCCACCCGGTTTC | 12449 |
rs256906129 | in-del | -/CCAA | | | intron-variant | Ccnf | Mm_Celera | 17:24231587 | TGCTCATGCTGGGGC[-/CCAA]CCAAGCTCAGGGTTT | 12449 |
rs256926995 | in-del | -/C/G/GG | | | intron-variant | Ccnf | GRCm38.p3 | 17:24232906 | ACTGTTTCTGAGGCA[-/C/G/GG]GGGGCAGCCTGTTCT | 12449 |
rs257094167 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24227276 | ACAGGGTTTCTCTGT[A/G]TAGCCCTGGCTGTCC | 12449 |
rs257122356 | in-del | -/TTCAGCGCGGCAGTTCA | | | intron-variant | Ccnf | GRCm38.p3 | 17:24245352 | TGGAGGCCGAGGCAG[-/TTCAGCGCGGCAGTTCA]GCGCGAGAGGAAAGC | 12449 |
rs257227060 | snp | A/C | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | GRCm38.p3 | 17:24235325 | GAGGAACAGGACAGG[A/C]AAGGTCTACTCCCCA | 12449 |
rs257317644 | snp | A/C | | | intron-variant | Ccnf | GRCm38.p3 | 17:24244449 | CACCACCAAAGGCTG[A/C]AGGAGACCAACACTC | 12449 |
rs257444813 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24229918 | ATGGTTGTGAGCCAC[C/T]AAGTGGTTGCTGGGA | 12449 |
rs257525088 | in-del | -/A | | | intron-variant | Ccnf | Mm_Celera | 17:24248917 | CAAAAAATAAAAATT[-/A]AAAAAAAAAAAAAAC | 12449 |
rs257531638 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24227406 | ACTTAAACGATCAGA[A/G]TGGGTAGAGTATATT | 12449 |
rs257557622 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24228080 | TGGGCCCAGGAGCCC[C/T]GGAGTAGCTGTGAAT | 12449 |
rs257569127 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24247619 | ACAGGGTTTCTCTGT[A/G]TAGCCCTGGCTGTTC | 12449 |
rs257570818 | in-del | -/A | | | intron-variant | Ccnf | GRCm38.p3 | 17:24229479 | ACAAACATCCGTAAC[-/A]AAAAATCTGATGCCC | 12449 |
rs257570898 | snp | A/T | | | intron-variant | Ccnf | Mm_Celera | 17:24251057 | CCCACGACTTCACAG[A/T]TAAGTAAAATCGTAG | 12449 |
rs257742642 | snp | A/C | | | intron-variant | Ccnf | GRCm38.p3 | 17:24248932 | TAAAAAAAAAAAAAA[A/C]GATTAAACCACGCAA | 12449 |
rs257817756 | snp | A/T | | | synonymous-codon | Ccnf | Mm_Celera | 17:24224990 | GTCCAGAAGGCTGCC[A/T]AGCAGTGTCTCCTCC | 12449 |
rs257862264 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24230073 | TGAAAAATTGCAAGA[A/G]GACATGTGGACTGAG | 12449 |
rs257906607 | snp | A/G | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24251967 | ATCCCCACAGCTTGG[A/G]TCAGCCTTCATCCCC | 12449 |
rs258070286 | snp | A/C | | | intron-variant, upstream-variant-2KB | Ccnf, Mir6965 | Mm_Celera | 17:24241310 | CCAAGGCAGTGTGGA[A/C]GCCTCAGGCTCTCTG | 12449 |
rs258074174 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24233464 | ATTGCTATGGGAGGG[C/T]TCAGCTCACTGTGGG | 12449 |
rs258103812 | snp | A/G | | | upstream-variant-2KB | Ccnf | Mm_Celera | 17:24252179 | CTGTCTCTTTTCCGG[A/G]AGACTATACTGTTTT | 12449 |
rs258140685 | snp | C/T | | | downstream-variant-500B | Ccnf | Mm_Celera | 17:24222966 | ACTCTTCTGACTTCT[C/T]GCTCTCCTGCATCTT | 12449 |
rs258231366 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | Ccnf, Mir5134 | Mm_Celera | 17:24236121 | TTTGAAGCCTGGAAT[-/AA]AGACAGTTGTGCTGG | 12449 |
rs258391624 | in-del | -/AACAACA | | | intron-variant | Ccnf | GRCm38.p3 | 17:24226289 | AACAACAACAACAAC[-/AACAACA]AAAGGCGATGCTTGG | 12449 |
rs258537702 | in-del | -/AC | | | intron-variant | Ccnf | GRCm38.p3 | 17:24243858 | AAATCTTAAAAAAAT[-/AC]ACACACACACACACA | 12449 |
rs258574717 | snp | A/C | | | intron-variant | Ccnf | Mm_Celera | 17:24225767 | GACCCAGATCTCCTC[A/C]ACTCCACAGAGAGGA | 12449 |
rs258610074 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24226004 | GAGGAGGCTGGGTGT[C/T]ACAGGATCCACAACT | 12449 |
rs258669709 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24226410 | TGCTGTGTCAAGAAG[A/G]AAACTGAGAGCTACC | 12449 |
rs258781890 | snp | A/G | | | synonymous-codon | Ccnf | Mm_Celera | 17:24231387 | GATGGACAGGCTGGT[A/G]TGCAGCAGGGTGAGC | 12449 |
rs258798435 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24246357 | GCAAAAACCCAGACG[C/T]GATTGGATGAGGCAC | 12449 |
rs259005037 | snp | C/T | | | intron-variant | Ccnf | GRCm38.p3 | 17:24245354 | GGAGGCCGAGGCAGG[C/T]GCGAGAGGAAAGCTA | 12449 |
rs259041660 | snp | C/T | | | intron-variant | Ccnf | Mm_Celera | 17:24246759 | TGTTCAGGACCTTGG[C/T]TGCTCTTGCAGAGGA | 12449 |
rs259163266 | snp | A/G | | | intron-variant | Ccnf | Mm_Celera | 17:24231502 | GGGATCTAGACAAGA[A/G]GGAGGAAAATGCCAC | 12449 |